European Thyroid Association and Cardiovascular and Interventional Radiological Society of Europe 2021 Clinical Practice Guideline for the Use of Minimally Invasive Treatments in Malignant Thyroid Lesions

in European Thyroid Journal
Authors:
Giovanni Mauri Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy
Division of Interventional Radiology, European Institute of Oncology, IRCCS, Milan, Italy

Search for other papers by Giovanni Mauri in
Current site
Google Scholar
PubMed
Close
,
Laszlo Hegedüs Department of Endocrinology, Odense University Hospital, University of Southern Denmark, Odense, Denmark

Search for other papers by Laszlo Hegedüs in
Current site
Google Scholar
PubMed
Close
,
Steven Bandula Interventional Oncology Service, University College Hospital, London, United Kingdom

Search for other papers by Steven Bandula in
Current site
Google Scholar
PubMed
Close
,
Roberto Luigi Cazzato Department of Interventional Radiology, University Hospital of Strasbourg, Strasbourg, France

Search for other papers by Roberto Luigi Cazzato in
Current site
Google Scholar
PubMed
Close
,
Agnieszka Czarniecka The Oncologic and Reconstructive Surgery Clinic, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Gliwice, Poland

Search for other papers by Agnieszka Czarniecka in
Current site
Google Scholar
PubMed
Close
,
Oliver Dudeck Center for Microtherapy, Klinik Hirslanden, Zurich, Switzerland

Search for other papers by Oliver Dudeck in
Current site
Google Scholar
PubMed
Close
,
Laura Fugazzola Department of Endocrinology and Metabolic Diseases, IRCCS Istituto Auxologico Italiano, Milan, Italy
Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy

Search for other papers by Laura Fugazzola in
Current site
Google Scholar
PubMed
Close
,
Romana Netea-Maier Division of Endocrinology, Department of Internal Medicine, Radboud University Medical Center, Nijmegen, The Netherlands

Search for other papers by Romana Netea-Maier in
Current site
Google Scholar
PubMed
Close
,
Gilles Russ Thyroid and Endocrine Tumors Unit, La Pitie-Salpetriere Hospital, Sorbonne University, Paris, France

Search for other papers by Gilles Russ in
Current site
Google Scholar
PubMed
Close
,
Göran Wallin Department of Surgery, Faculty of Medicine and Health, Örebro University, Örebro, Sweden

Search for other papers by Göran Wallin in
Current site
Google Scholar
PubMed
Close
, and
Enrico Papini Department of Endocrinology & Metabolism, Ospedale Regina Apostolorum, Albano, Italy

Search for other papers by Enrico Papini in
Current site
Google Scholar
PubMed
Close
Free access

Sign up for journal news

The growing detection of papillary thyroid microcarcinomas (PTMCs) is paralleled by an increase in surgical procedures. Due to the frequent indolent nature, cost, and risk of surgery, active surveillance (AS) and ultrasound-guided minimally invasive treatments (MITs) are in suitable cases of incidental PTMC proposed as alternatives to thyroidectomy. Surgery and radioiodine are the established treatments for relapsing cervical differentiated thyroid carcinoma (DTC) metastases. But radioiodine refractoriness, risk of surgical complications, adverse influence on quality of life, or declining repeat surgery have led to AS and MIT being considered as alternatives for slow-growing DTC nodal metastases. Also, for distant radioiodine-refractory metastases not amenable to surgery, MIT is proposed as part of a multimodality therapeutic approach. The European Thyroid Association and the Cardiovascular and Interventional Radiological Society of Europe commissioned these guidelines for the appropriate use of MIT. Based on a systematic PubMed search, an evidence-based approach was applied, and both knowledge and practical experience of the panelists were incorporated to develop the manuscript and the specific recommendations. We recommend that when weighing between surgery, radioiodine, AS, or MIT for DTC, a multidisciplinary team including members with expertise in interventional radiology assess the demographic, clinical, histological, and imaging characteristics for appropriate selection of patients eligible for MIT. Consider TA in low-risk PTMC patients who are at surgical risk, have short life expectancy, relevant comorbidities, or are unwilling to undergo surgery or AS. As laser ablation, radiofrequency ablation, and microwave ablation are similarly safe and effective thermal ablation (TA) techniques, the choice should be based on the specific competences and resources of the centers. Use of ethanol ablation and high-intensity focused ultrasound is not recommended for PTMC treatment. Consider MIT as an alternative to surgical neck dissection in patients with radioiodine refractory cervical recurrences who are at surgical risk or decline further surgery. Factors that favor MIT are previous neck dissection, presence of surgical complications, small size metastases, and <4 involved latero-cervical lymph nodes. Consider TA among treatment options in patients with unresectable oligometastatic or oligoprogressive distant metastases to achieve local tumor control or pain palliation. Consider TA, in combination with bone consolidation and external beam radiation therapy, as a treatment option for painful bone metastases not amenable to other established treatments.

Abstract

The growing detection of papillary thyroid microcarcinomas (PTMCs) is paralleled by an increase in surgical procedures. Due to the frequent indolent nature, cost, and risk of surgery, active surveillance (AS) and ultrasound-guided minimally invasive treatments (MITs) are in suitable cases of incidental PTMC proposed as alternatives to thyroidectomy. Surgery and radioiodine are the established treatments for relapsing cervical differentiated thyroid carcinoma (DTC) metastases. But radioiodine refractoriness, risk of surgical complications, adverse influence on quality of life, or declining repeat surgery have led to AS and MIT being considered as alternatives for slow-growing DTC nodal metastases. Also, for distant radioiodine-refractory metastases not amenable to surgery, MIT is proposed as part of a multimodality therapeutic approach. The European Thyroid Association and the Cardiovascular and Interventional Radiological Society of Europe commissioned these guidelines for the appropriate use of MIT. Based on a systematic PubMed search, an evidence-based approach was applied, and both knowledge and practical experience of the panelists were incorporated to develop the manuscript and the specific recommendations. We recommend that when weighing between surgery, radioiodine, AS, or MIT for DTC, a multidisciplinary team including members with expertise in interventional radiology assess the demographic, clinical, histological, and imaging characteristics for appropriate selection of patients eligible for MIT. Consider TA in low-risk PTMC patients who are at surgical risk, have short life expectancy, relevant comorbidities, or are unwilling to undergo surgery or AS. As laser ablation, radiofrequency ablation, and microwave ablation are similarly safe and effective thermal ablation (TA) techniques, the choice should be based on the specific competences and resources of the centers. Use of ethanol ablation and high-intensity focused ultrasound is not recommended for PTMC treatment. Consider MIT as an alternative to surgical neck dissection in patients with radioiodine refractory cervical recurrences who are at surgical risk or decline further surgery. Factors that favor MIT are previous neck dissection, presence of surgical complications, small size metastases, and <4 involved latero-cervical lymph nodes. Consider TA among treatment options in patients with unresectable oligometastatic or oligoprogressive distant metastases to achieve local tumor control or pain palliation. Consider TA, in combination with bone consolidation and external beam radiation therapy, as a treatment option for painful bone metastases not amenable to other established treatments.

Scope of the Document

During the last decades, the incidence of differentiated thyroid cancer (DTC) is continuously rising in Europe and is estimated as high as 9 and 3 cases per 100,000 person-years in the female and male population, respectively [1]. Even if epidemiological differences are reported among different countries, papillary thyroid cancer (PTC) represents 80–85% and follicular cancer about 5–10% of cases, while medullary and anaplastic cancer account for the remaining [2]. Most DTCs are not aggressive tumors, as the disease-specific mortality rate is 0.7 and 0.5% per 100,000 person-years for women and men, respectively [1]. After successful initial treatment, local recurrences of PTC were registered during a 10-year follow-up in about 1.4% of patients and most of them occurred within 8 years [3]. However, the risk of recurrence or persistent structural disease rapidly increases in patients with advanced stage at diagnosis. Disease persistence or relapse are expected in <5, 6–20, and >20% of patients classified as low, intermediate, or high risk, respectively, according to the ATA risk of recurrence staging system [4].

So, the majority of DTCs are successfully cured with initial surgical treatment, followed, if needed, by radioiodine ablation (RAI) [4]. But, a few issues remain unsettled.

The growing incidental detection of papillary thyroid microcarcinomas (PTMCs) is paralleled by the progressive increase in surgical thyroid procedures [5]. Due to the frequently indolent nature of PTMC and the cost and risk of surgery, active surveillance (AS) and ultrasound (US)-guided minimally invasive treatments (MITs) are proposed as alternative management options to thyroidectomy for selected incidental PTMC [4, 6-8].

Moreover, after complete surgical resection, a follow-up by US may detect local recurrence in up to 7% of DTC as a whole and in up to 2.4% of PTMC patients [9, 10]. Repeat compartment-oriented surgery is the established therapeutic approach for DTC metastases which progressively grow during follow-up, but lymphadenectomy results in biochemical remission only in 21–61% of these patients [11, 12]. Also, management problems may occur because of the absence of radioiodine uptake, the increased risk of surgical complications, the unfavorable influence of further surgery on quality of life, or the patient’s declining repeat surgery after previous neck dissection. For these reasons, and the frequently indolent course of DTC lymph-node recurrences, current thyroid cancer guidelines suggest considering AS for cervical nodal metastases with a diameter ≤10 mm that appear as slow-growing [4]. As an alternative option, various image-guided MITs are now proposed as outpatient therapy of incidentally found indolent cervical DTC recurrences [13].

DTCs can result in distant metastases in up to 10% of cases, with lung and bone representing the 2 most commonly involved organs [14]. Various therapy options are currently available in metastatic patients, including RAI treatment, tyrosine-kinase inhibitors, surgery, radiation therapy (external beam radiation therapy [EBRT]), and MIT [15]. MIT is proposed in the multidisciplinary approach to patients with RAI refractory metastatic thyroid cancer who are fragile or not amenable to surgery, with the aim of achieving local control and/or pain palliation with minimal invasiveness of lung, bone, and liver disease.

Currently, the major thyroid cancer guidelines dedicate only a marginal attention to the use of MIT for malignant thyroid disease management [4, 16]. As the available information and the technical resources are rapidly evolving in this area [17], scope of the present guideline is to provide a clinical practice guide for the appropriate use of MIT, based on the best available scientific evidence and the authors’ expertise.

Methodology and Grading of Evidence

The Executive Committees of the European Thyroid Association (ETA) and the Cardiovascular and Interventional Radiological Society of Europe (CIRSE) commissioned development of these guidelines to a task force led by 3 chairpersons (L.H., G.M., and E.P.). This team proposed a group of other 8 authors (4 from CIRSE and 4 from ETA) to compose the guideline panel. The proposal was based on clinical experience, scholarly approach, being an ETA or/a CIRSE member, and willingness to participate. The ETA and CIRSE guideline boards approved the composition of this team.

The relevant literature was taken into consideration using a systematic PubMed search. An evidence-based approach was applied, and both the knowledge and the practical experience of the panelists were incorporated to develop the manuscript and the specific recommendations. The Grading of Recommendations, Assessment, Development, and Evaluation system was used when rating the strength of the recommendations and the quality of evidence [18].

In accordance with previous guidelines, we used the following coding system: strong recommendation indicated by 1 and weak recommendation, or suggestion, indicated by 2. The evidence grading is given as follows: very-low-quality (ØOOO), low-quality (ØØOO), moderate-quality (ØØØO), and high-quality evidence (ØØØØ). An electronic questionnaire was built on the Google Forms platform (Google LLC, Mountain View, CA, USA) and was disseminated to all participants and 2 Delphi rounds were performed to assess consensus.

Following discussions and after the task force had reached consensus, the draft was sent to the Guideline Boards for comments and thereafter posted on the ETA websites for 4 weeks for critical evaluation by the members. The received comments were evaluated by the authors and the guideline board, and the resulting changes were incorporated into the final document before submission to the European Thyroid Journal.

Techniques for Image-Guided Ablation of Thyroid Lesions: An Overview

As a rule, before MIT, the diagnosis of DTC recurrence must be confirmed by fine needle aspiration or core-needle biopsy.Local anesthesia, with or without conscious sedation depending on the patients’ wish, is preferred for the ablation of PTMC, cervical lymph-node metastases, and distant metastases in case of short procedural times. General anesthesia is preferred for the ablation of distant metastases requiring protracted treatment time (over 60 min).

Ethanol Ablation

Ethanol affects the tissues by inducing coagulative necrosis and endothelial damage resulting in thrombosis of small vessels, ischemic injury, and permanent tissue ablation. 21–27-gauge (G) needles are used, attached to a 1–5 mL syringe containing 95–99.9% ethanol. Small amounts (0.1–0.5 mL) of ethanol are slowly injected, according to size and shape of the lesion to be treated, with constant US monitoring of the diffusion. Local anesthesia is generally used before ethanol ablation (EA). Immediately after the injection of ethanol, the treated area becomes echogenic on US, masking the needle tip and blurring the image of the area. After 1–3 min, the echogenic area decreases, and the needle tip is eventually repositioned into an untreated zone. Ethanol injections are repeated until the entire targeted tissue appears completely treated. Ethanol leakage outside the lesion may occur, resulting in severe pain and requiring the immediate cessation of injection [19-21].

Thermal Ablation

Laser Ablation

Laser is a focused beam of light energy, usually generated by a diode or a Nd:YAG source and delivered through an optical fiber into the target tissue [22-24]. In laser ablation (LA), the optical fibers are inserted through a 21 G flexible guiding needle. The number of fibers to be inserted and the path to be followed are planned by the operator according to size and shape of the target lesion. Needle insertion along the major axis of the target lesion allows a repeat pullback for multiple illuminations. Injection of sterile saline or glucose solution around the target lesion can be performed to obtain a safety distance between the lesion and surrounding critical structures (“hydrodissection”). Hyperechoic signals, due to the formation of gas microbubbles, occurs during the ablation process, reflecting the heat-induced changes of the tissue. Most often, a fixed power protocol is used with LA, changing the total amount of energy delivered according to target tumor size and US modifications [25, 26].

Radiofrequency Ablation

An alternating electric current is applied to the target tissue via an electrode needle. The electric current rapidly oscillates tissue ions, creating frictional heating in areas of high current density adjacent to the electrode. Additional growth of the ablation zone is primarily due to thermal diffusion [13, 27]. Monopolar electrodes, with collecting pads and bipolar devices, without pads, are available [27, 28]. Short (7–10 cm length) and thin (17–19 G) devices, appropriate for use in the neck region, are also available. Hydrodissection with a glucose solution can be used to increase the safety of the procedure. The electrode is introduced under US guidance into the target lesion, and in large lesions, a continuous repositioning of the applicator (“moving shot” technique) is performed to ablate the entire lesion [27, 28]. The appearance of hyperechoic signals close to the electrode tip indicates the development of tissue changes, while a steep rise in tissue impedance demonstrates the achievement of tissue necrosis [27, 28].

Microwave Ablation

With microwave ablation (MWA), high-frequency (MHz to GHz range) electromagnetic energy passes unimpeded into the tissue and induces hyperthermia by rapid oscillation of water molecules. This direct tissue heating is less susceptible to the perfusion cooling of blood supply, thereby allowing larger volume and more consistent tissue necrosis. The technique is otherwise identical to RFA, by means of probe introduction into the lesion under US guidance, followed by tumor coverage via multiple overlapping burns. Internally cooled antennas require a single low-loss cable and 14–17 G probes. Probe dimension is chosen according to the target tumor to be treated (either superficial neck lesions or deep liver/lung/bone metastases) [29, 30].

Cryoablation

Localized tissue necrosis is achieved by inducing tissue hypothermia down to −40 to −140°C. Inside the needle probes, pressured gas (most frequently argon) passes through a narrow channel and is released within the device tip. Expansion of the gas causes rapid cooling via the Joule-Thompson effect, and an “ice ball” is formed in the adjacent tissue. Probes producing ice balls of various sizes are available which can be combined to produce a treatment volume which conforms to the target tumor. The ice ball is readily visible on computerized tomography and magnetic resonance and, less distinctly, with US examination, thus allowing intraprocedural monitoring – particularly useful when treating lesions close to critical structures. In cases at risk of complications, and for the protection of the skin in superficial tumors, hydrodissection should be preliminarily performed as for the heat-related techniques.

The mechanism of tissue injury is incompletely understood, but osmotic insult, cell wall crystal injury, and microvascular thrombosis may all contribute to ablation. Unlike hyperthermia-induced necrosis, there is less disruption of the tissue architecture, partly reducing the risk of vascular and nerve injury, even if major complications may occur [31, 32]. This technique is generally less painful than heat-based technologies and is especially suitable for the treatment of superficial tumors on an outpatient basis.

The complication rate is not negligible after cryoablation. Pneumothorax, pleural effusion, and hemoptysis are reported in 61.7, 70.5, and 36.8% of lung cancer treatments [33]. In a recent series of 23 patients with painful sacral metastases treated with either RFA or cryoablation, no major complications occurred, but the frequency of minor complications was 23% [34].

High-Intensity Focused Ultrasound Ablation

High-intensity focused ultrasound ablation is the only completely noninvasive ablation technique. Ultrasonic energy, in the 20 kHz–200 Mhz range, induces molecular vibration, frictional heating, and cavitation. By focusing the energy from a probe outside the patient into a small volume, tissue destruction can be achieved within the target tumor without affecting intervening structures. Multiple overlapping ablation volumes may allow a complete target ablation. Care must be taken to avoid subtotal treatment because computerized control may prevent the ablation of peripheral areas close to critical structures [35, 36].

Criteria for the Selection of Oncologic Patients Who Are Candidates for Minimally Invasive Treatment or a Multimodality Approach

Indications for image-guided MITs in thyroid malignancies should be evaluated by a multidisciplinary team including experts in both traditional and image-guided interventional treatment modalities [13]. The choice of the appropriate MIT procedure, whether EA, LA, RFA, MWA, or high-intensity focused ultrasound ablation, depends on type and location of tumor, the team’s experience, local technical resources, and the patients’ characteristics [37]. Patients should always be informed about advantages and limitations of MIT in comparison with the other management options.

The use of MIT may be considered in patients with DTC in the following conditions:

1. PTMC

2. Unresectable thyroid cancer

3. Neck lymph-node recurrences of DTC

4. Distant metastases

In incidentally discovered low-risk PTMC in patients who are not eligible for or decline surgery, MIT may be considered as an alternative option to AS [38-42]. A cytology suspicion of aggressive subtypes of thyroid carcinoma (e.g., tall cell, insular, and columnar cell), imaging detection of extrathyroidal growth or multiple neoplastic foci, presence of lymph node or distant metastases, and/or a worrisome molecular pattern (e.g., the detection of TERT promoter and TP53 mutations) contraindicate the use of MIT [38-42]. Moreover, due to the absence of comorbidities, higher risk of lymph node metastases and need of life-long follow-up, immediate surgery remains the best therapeutic approach to young subjects [40].

In patients with unresectable thyroid cancer, MIT should be considered as a palliative procedure for rapidly decreasing tumor burden and improving local symptoms, mainly in the context of multimodality treatment [43-45]. In patients with progressive RAI refractory cervical recurrences, who are at surgical risk or decline further surgery, MIT may be employed as an alternative to surgical neck dissection. MIT should be mainly considered in fragile patients with limited life expectancy, previous neck dissection, surgical complications, small size (<20 mm) metastases, and limited number (<4) of involved lymph nodes in the latero-cervical compartments [26, 29, 30, 46, 47]. TA should be discouraged, except for palliative purposes, in patients with extensive lymph node involvement, central recurrences, evidence of radioiodine uptake, or clinical and histological factors suggesting an aggressive disease.

In selected patients with distant RAI refractory metastases from DTC, MIT may be proposed within the multimodality approach to advanced disease, with palliative intent (i.e., symptom relief) or in selected cases to achieve local tumor control. TA is, in particular, indicated in patients with bone metastases that are resistant to, or that could successively use, EBRT for preventing adverse skeletal events or for delaying systemic treatment [48, 49].

Clinical Use in Thyroid Malignancies

Primary Thyroid Cancer

MIT has been applied in the treatment of primary thyroid cancer, mainly in patients with incidentally diagnosed PTMC [40, 44, 50-54] and only rarely in patients with other types of primary thyroid tumors [43-45].

Papillary Thyroid Microcarcinoma

Due to the frequent indolent nature of PTMC, and the cost and risk of surgery, AS and MIT are considered as alternative management options to thyroidectomy for incidental PTMC [8, 55, 56]. Since the first feasibility study using laser for nonsurgical management of PTMC [57], US-guided treatments with laser, RFA, and MWA have been documented by several centers [40, 44, 50-54]. Three systematic reviews and meta-analyses have provided high-quality evidence of the efficacy and safety of RFA, MWA, and LA. The first study, based on 503 PTMCs with follow-up ranging from 8 to 53 months, demonstrated neither local tumor recurrence nor distant metastases after TA [6]. Cervical lymph node metastases were detected, at 24 and 30 months, respectively, in 2 patients (0.4%). There were no major complications, and minor complications (transient dysphonia, intrathyroidal bleeding, and parenchymal edema) ranged from 3.4 to 19.0% [6]. A second meta-analysis, including 715 patients with follow-up ranging from 8 to 26 months, registered complete disappearance in 57.6% of treated PTMC. Scar-like remnants, devoid of viable cancer cells at FNA, were observed in the remaining cases. Major (persistent dysphonia) and minor complications were reported in 0.7 and 3.2% of cases, respectively, with a 0.4% local recurrence rate [7]. A third meta-analysis, analyzing results of RFA, MWA, and LA in 1,284 PTMCs, demonstrated that complete disappearance was the highest (76.2%) and recurrence rate the lowest (0.01%) after RFA, compared with the other 2 methods, although not statistically significant. Conversely, the complication rate was lower with LA (0.9%) than with RFA (1.7%) and MWA (6.0%). No distant metastases occurred during the 7.8 months median follow-up [41]. Notably, in the reported meta-analysis, the follow-up was generally short for thyroid cancer surveillance, and the authors never mentioned the thyroglobulin level. Randomized head-to-head trials of TA versus surgery are lacking but recent studies report the outcomes of large retrospective series. Ninety-four patients treated with RFA were compared to 80 patients treated surgically during the same period [58]. After 5 years of follow-up, clinical outcomes were similar but procedure time, hospital stay, and cost of RFA were lower than those with surgery. The surgery group had significantly more major complications and lower posttreatment thyroid-related quality of life. In another study, 81 patients were treated with either surgery or LA with a 49-month mean follow-up; 94.4% of the ablated lesions completely disappeared and 5.6% remained as scar-like zones. Complication rates and recurrence rates did not differ significantly between the LA (2.8 and 5.6%, respectively) and the surgical group (6.7 and 6.7%, respectively). Mean hospital stay and procedure time were also shorter in the LA group. No distant metastases occurred in either group [59]. Robust comparative data are available in 2 meta-analyses. The first, including 867 patients, demonstrated that recurrence rate and recurrence-free survival following TA and surgery were similar, but that TA had a significantly lower complication rate (odds ratio [OR] 0.24), postoperative length of stay, and costs (pooled standard mean difference −1.69) [60]. The second meta-analysis, involving 1,289 patients, demonstrated that the risk of hoarseness (OR 0.33), late hypothyroidism (OR 0.31), and postoperative pain (OR 0.35) was lower and the hospitalization time was shorter (SMD −4.01) in the TA group. The TA group also obtained a better cosmetic result while other symptomatology did not differ significantly compared to surgery [61].

EA was employed from 2010 to 2017, in a small series of 15 patients with PTMC. After ethanol injection, tumor shrinkage and absence of Doppler flow was demonstrated in all cases. Neither major complications nor local recurrence or nodal metastases were reported [62].

AS has been proposed as an alternative to immediate surgery for PTMC, balancing the low probability of cancer progression, with prevention of surgical complications and late hypothyroidism [55]. No head-to-head comparison of TA versus AS is available, but the advantage of the ablation of the neoplastic area is potentially relevant. During a 5-year AS period, linear growth of PTMC volume has been reported in 12–23% of cases, while a minority of patients, especially among the young, developed extrathyroidal spread and cervical metastases after several years of observation [56, 63, 64]. Finally, as from 8.7 to 32.0% of patients in AS programs undergo delayed surgery for reasons unrelated to cancer growth [6], TA could also prevent the anxiety caused by awareness of harboring a tumor which may grow and eventually need more aggressive surgical removal [65]. The main advantages of TA are the possibility of offering an active treatment, which seems to be as effective as surgical removal, in an outpatient setting, with reduced invasiveness, no need of general anesthesia, and low risk of complications and hypothyroidism [17].

Unresectable Thyroid Cancer

A different scenario is represented by using MIT for tumor volume reduction and control of threatening local symptoms in unresectable primary DTC, medullary, or anaplastic carcinomas. Few data are available on this topic, but a mean volume reduction of 51% was observed in a series of inoperable DTCs. Importantly, RFA was not effective if the tumors had overt vascular encasement or massive calcification due to the difficult approach and the insufficient burden ablation [66]. In a large series of DTCs invading the airways, the volume reduction rate was 81.2% and complete disappearance rate, 72.1% (mean follow-up, 47.9 months). The efficacy decreased significantly according to the degree of tracheal abutment of the tumors [35].

Both LA and RFA may be used for the management of medullary thyroid cancer in patients not amenable to surgery [67, 68]. A few case reports demonstrated the efficacy of TA for short-term local control of medullary thyroid cancer, but the available evidence is still limited.

The feasibility of LA has been also reported for some anaplastic thyroid cancers, usually with minor short-term effects on symptoms and without effects on thyroid volume reduction [43-45]. Thus, treatment of inoperable anaplastic or medullary thyroid carcinoma with TA is characterized by inconsistent outcomes, and it should be considered only in patients with no other possible option, with palliative intent. In these cases, MIT may be part of a multimodality approach to advanced thyroid cancer but should never delay the use of systemic therapy and EBRT for this deadly disease (Tables 1, 2).

Table 1.

Indications for use of MITs in PTMCs

Table 1.
Table 2.

Summary of recommendations

Table 2.

Follicular Neoplasms

Few reports consider the use of TA for thyroid nodules with a cytological diagnosis of follicular neoplasm. In a 5-year follow-up study, 8 of 10 follicular lesions <2.0 cm in largest diameter completely disappeared, and 2 showed 97% volume reduction after RFA. There were no recurrences or distant metastases during the follow-up period [69]. In a second study, 6 thyroid lesions with follicular cytology and negative BRAF and NRAS molecular testing were treated with RFA and followed up until 24 months [70]. Two lesions regrew after treatment and were surgically excised. Histological examination revealed a follicular carcinoma and a follicular neoplasm of indeterminate malignant behavior. Therefore, surgery remains the established standard of care for the management of thyroid nodules with Bethesda IV cytology because of the risk of delayed diagnosis, and distant metastasis, in those follicular lesions that correspond to follicular thyroid cancers. TA should be restricted to patients with follicular lesions who are at surgical risk and present favorable US features and negative molecular testing as an alternative to clinical surveillance.

Neck Recurrences of Thyroid Cancer

The majority of DTCs are successfully cured with initial surgical treatment, followed, if needed, by RAI ablation [15]. Even after apparently successful treatment, recurrence can occur in the thyroid bed and/or as nodal metastases. Repeat compartment-oriented surgery is the established therapeutic approach for DTC recurrences but lymphadenectomy results in biochemical and structural remission only in some of these patients [71]. Thus, AS and MIT can be considered an alternative to surgery for selected patients with cervical DTC metastases [15].

EA has been reported as effective in local disease control in a few single-center case series [19, 72, 73]. The largest retrospective study, including 109 neck lymph node metastases, with a 38-month median follow-up, demonstrated complete response in 84% [19]. Up to 5 EA sessions were needed for complete ablation and, despite reporting no major complications, local pain and side effects may occur frequently. The major limitations of EA are the uneven and unpredictable area of ablation and risk of ethanol seeping into neck tissues [8]. A retrospective study comparing the outcomes of 42 patients with recurrence of DTC, treated either with EA or RFA, found no recurrences in the RFA group (61 months follow-up), while 5 of 21 (23%) metastases had local progression at 4–11 months after EA [74]. Retrospective and prospective studies have demonstrated efficacy of RFA, LA, and MWA for local control of DTC recurrence [29, 47, 75, 76]. A 2016 meta-analysis, including 255 metastatic lesions treated with US-guided RFA, demonstrated a significant tumor volume decrease at 6 months follow-up [77]. A second meta-analysis, evaluating the efficacy and safety of RFA and EA for treating locally recurrent thyroid cancer, included 415 thyroid lesions [78]. The complete disappearance rate after RFA was 68.8% and the recurrence rate, 0.0%, with a complication rate of 1.6%.

Head-to-head prospective studies of TA versus surgery are unavailable, but a few papers retrospectively compared the outcomes of RFA and surgical neck dissection. In a study in patients with <20-mm cervical DTC recurrences, 27 treated with RFA and 46 treated with surgery, the 3-year recurrence-free survival was similar in the 2 groups (96.0 and 92.6%, respectively). Major complications, mostly hypocalcemia, occurred only in the re-operated group [76]. In a long-term retrospective study, with propensity score adjustment, 2 cohorts of 70 patients with locally recurrent thyroid cancer underwent either RFA or repeat surgery. The recurrence-free survival rates in the RFA and in the surgery groups were similar (89.4 vs. 94.5% at 6 years, respectively) with no significant differences in mean posttreatment serum Tg levels. Hypocalcaemia and overall complication rates were significantly higher in the surgery group (7 cases in the RFA vs. 27 cases in the surgery group) [79].

LA was reported feasible in RAI refractory cervical DTC recurrence following cervical lymph-node dissection. A prospective trial in 8 non-RAI-avid cervical recurrences demonstrated a mean volume decrease from 0.64 to 0.07 mL at 12-months, with undetectable Tg levels in 60% of cases [75]. In 46 18FDG-PET/computerized tomography-positive nodal metastases followed up for 30 months [46], local control was obtained in 40 of 46 (86.9%) lymph nodes, with no detectable residual disease in 79% of patients.

Also, efficacy of LA was demonstrated in a patient with medullary thyroid cancer recurrence [26]. In a retrospective study of 24 lymph node metastases of PTC treated with MWA, nearly complete disappearance was achieved with no late recurrence reported during a 32-month follow-up [30]. A prospective study of 23 cervical PTC recurrences, with an up to 18-month follow-up, demonstrated a 91% mean volume reduction at the final follow-up. Complete disappearance in 30.4% and persistence as scar-like areas in 52.2% were reported. One patient experienced transient dysphonia, but no permanent complications occurred [29].

Notably, TA of thyroid cancer metastases is followed by a rapid increase of serum Tg levels during the following 48 h. After complete destruction of lymph node metastases, serum Tg progressively decreases to undetectable levels and becomes a sensitive blood marker for monitoring potential disease relapse [25, 75]. Similarly, serum calcitonin level may be used as an effective marker for monitoring the local control of medullary thyroid cancer metastases after thermal ablation of nodal recurrences [26].

Distant Metastases

Follicular and, to a lesser extent, papillary thyroid carcinomas result in distant metastases in up to 10% of cases, with lung and bone representing the 2 most commonly involved organs [14]. Various therapy options are currently available in metastatic patients, including RAI treatment, tyrosine-kinase inhibitors, surgery, EBRT, and MIT [15]. MIT is proposed in the multidisciplinary approach to patients with RAI refractory metastatic thyroid cancer who are fragile or not amenable to surgery. The aim being local disease control in oligometastatic or oligoprogressive patients and/or pain palliation with minimal invasion. However, outcome evidence is limited and of modest quality.

Lung Metastases

RFA treatment of 1,037 lung metastases from primary cancers of colon, rectum, kidney, and thyroid (the latter accounting for only 3%), treated up to 4 times without major complications, demonstrated progression-free survival and local tumor progression rates of 40.2 and 13.1%, and 5.9 and 11.0%, at 1 and 4 years, respectively [80]. Factors associated with poor overall and progression-free survival were primary disease other than colon or kidney, disease-free interval ≤1-year, tumor size >20 mm, and >2 pulmonary metastases. Pneumothorax was the most common adverse event, occurring in 67% of ablation procedures and requiring treatment in 28% of cases, while the 30-day mortality was 0.35%.

Bone Metastases

The most common site of bone metastases from thyroid cancer is the spine, severely affecting the quality of life and frequently resulting in focal neurologic symptoms and pathologic fractures. Treatment options, besides repeated RAI therapy in cases with persistent radioiodine uptake, include surgical resection, vertebroplasty, EBRT, and MIT. In a single-arm prospective multicenter study [81], RFA significantly relieved pain intensity from bone metastases at the 3-month follow-up. Three major adverse effects (refractory pain and neural damages) were reported. Similarly, a study using cryoablation [82] reported a mean score for worst pain in a 24-h period decreasing from 7.1/10 before treatment to 5.1/10 and 1.4/10 at 1- and 24-week follow-up, respectively; 83% of patients reporting opioid use before cryoablation reduced their intake during follow-up, and only 1 case of infection was registered. LA was employed for the management of 6 DTC metastatic lesions resistant to high-dose RAI therapy, followed by EBRT and on opioid analgesics [83]. At 6 months, imaging showed massive reduction of tumor burden associated with a significant decrease in all pain variables. No major complications occurred, and daily opioid requirement significantly decreased. Secondary fractures represent the most common major adverse event following bone tumor ablation [84, 85]. Therefore, TA should be combined, especially for weight-bearing bones, with bone consolidation by osteoplasty or osteosynthesis [86, 87].

Liver Metastases

There is considerable experience with TA of liver lesions, including metastases from different tumors [88, 89]. After RFA in 512 colorectal liver metastases, local tumor progression-free and overall survival were 72 and 30% at 10 years, and 72 and 28% at 10 and 15 years, respectively [89]. Small ablation margins (<5 mm) and large tumor size (>2 cm) were factors affecting complete ablation and local tumor progression [88, 89]. Importantly, major complications following MIT were rare (1–7%) [88, 89], and percutaneous TA was safely combined with systemic treatments. Only sporadic reports are available on TA outcomes in liver metastases of other origins, including thyroid cancer. Use of LTA and RFA were described in single case-reports [90, 91] as effective for rapid tumor burden decrease and associated with marked, but temporary, symptom improvement. Therefore, TA should be considered in a multimodality approach to DTC patients who are at surgical risk and in whom other treatment modalities are ineffective. Anecdotal reports are also available for RFA treatment of liver metastases from medullary thyroid cancer [67].

Concluding Remarks

The major hindrances before implementing these technologies in the treatment of malignant thyroid disease are the same as those for benign thyroid disease, which are primarily, lack of guidelines and access to these technologies for thyroid disease [92, 93]. Realizing this has been among the main drivers of the present guideline and the ambition to establish teaching courses in the near future.

Conflict of Interest Statement

G.M.: consultancy from Elesta SrL, speaking fee from GE, Advisory Board for Boston Scientific. All other authors declare they have no conflicts of interest to declare.

Funding Sources

No funds were received for the present work.

Author Contributions

All authors contributed to the idea, gathered the information, interpreted the data, and wrote and accepted the final version of the manuscript.

Footnotes

verified

References

  • 1

    European Network of Cancer Registries Factsheets [Internet]. [cited 2021 Apr 7]. Available from: https://www.encr.eu/sites/default/files/factsheets/ENCR_Factsheet_Thyroid_2017-2.pdf.

    • PubMed
    • Export Citation
  • 2

    Figge JJ . Epidemiology of thyroid cancer. In: Thyroid cancer (second edition): a comprehensive guide to clinical management. Totowa, NJ: Humana Press; 2006. p. 913.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 3

    Durante C , Montesano T, Torlontano M, Attard M, Monzani F, Tumino S, et al.. Papillary thyroid cancer: time course of recurrences during postsurgery surveillance. J Clin Endocrinol Metab. 2013 Feb;98(2):63642.http://dx.doi.org/10.1210/jc.2012-3401.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 4

    Haugen BR , Alexander EK, Bible KC, Doherty GM, Mandel SJ, Nikiforov YE, et al.. 2015 American thyroid association management guidelines for adult patients with thyroid nodules and differentiated thyroid cancer: the American thyroid association guidelines task force on thyroid nodules and differentiated thyroid Cancer. Thyroid. 2016 Jan;26(1):1133.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 5

    Lim H , Devesa SS, Sosa JA, Check D, Kitahara CM. Trends in thyroid cancer incidence and mortality in the United States, 1974–2013. JAMA. 2017 Apr;317(13):133848.http://dx.doi.org/10.1001/jama.2017.2719.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 6

    Cho SJ , Baek JH, Chung SR, Choi YJ, Lee JH. Thermal ablation for small papillary thyroid cancer: a systematic review. Thyroid. 2019 Dec;29(12):177483. http://dx.doi.org/10.1089/thy.2019.0377.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 7

    Choi Y , Jung S-L. Efficacy and safety of thermal ablation techniques for the treatment of primary papillary thyroid microcarcinoma: a systematic review and meta-analysis. Thyroid. 2020 May;30(5):72031.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 8

    Mauri G , Orsi F, Carriero S, Della Vigna P, De Fiori E, Monzani D, et al.. Image-guided thermal ablation as an alternative to surgery for papillary thyroid microcarcinoma: preliminary results of an Italian experience. Front Endocrinol. 2021;11:575152.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 9

    Chereau N , Oyekunle TO, Zambeli-Ljepović A, Kazaure HS, Roman SA, Menegaux F, et al.. Predicting recurrence of papillary thyroid cancer using the eighth edition of the AJCC/UICC staging system. Br J Surg. 2019 Jun;106(7):88997. http://dx.doi.org/10.1002/bjs.11145.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 10

    Roti E , degli Uberti EC, Bondanelli M, Braverman LE. Thyroid papillary microcarcinoma: a descriptive and meta-analysis study. Eur J Endocrinol. 2008 Dec;159(6):65973.http://dx.doi.org/10.1530/EJE-07-0896.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 11

    Urken ML , Milas M, Randolph GW, Tufano R, Bergman D, Bernet V, et al.. Management of recurrent and persistent metastatic lymph nodes in well-differentiated thyroid cancer: a multifactorial decision-making guide for the thyroid cancer care collaborative. Head Neck. 2015 Apr;37(4):60514. http://dx.doi.org/10.1002/hed.23615.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 12

    Al-Saif O , Farrar WB, Bloomston M, Porter K, Ringel MD, Kloos RT. Long-term efficacy of lymph node reoperation for persistent papillary thyroid cancer. J Clin Endocrinol Metab. 2010;95(5):218794.http://dx.doi.org/10.1210/jc.2010-0063.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 13

    Mauri G , Gennaro N, Lee MK, Baek JH. Laser and radiofrequency ablations for benign and malignant thyroid tumors. Int J Hyperthermia. 2019 Oct;36(2):1320. http://dx.doi.org/10.1080/02656736.2019.1622795.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 14

    Durante C , Haddy N, Baudin E, Leboulleux S, Hartl D, Travagli JP, et al.. Long-term outcome of 444 patients with distant metastases from papillary and follicular thyroid carcinoma: benefits and limits of radioiodine therapy. J Clin Endocrinol Metab. 2006;91(8):28929.http://dx.doi.org/10.1210/jc.2005-2838.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 15

    Haugen BR , Alexander EK, Bible KC, Doherty GM, Mandel SJ, Nikiforov YE, et al.. 2015 American thyroid association management guidelines for adult patients with thyroid nodules and differentiated thyroid cancer: the American thyroid association guidelines task force on thyroid nodules and differentiated thyroid cancer. Thyroid. 2016 Jan;26(1):1133.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 16

    Filetti S , Durante C, Hartl D, Leboulleux S, Locati LD, Newbold K, et al.. Thyroid cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2019 Dec;30(12):185683.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 17

    Hegedüs L , Miyauchi A, Tuttle RM. Nonsurgical thermal ablation of thyroid nodules: not if, but why, when, and how? Thyroid. 2020 Dec;30(12):16914.

  • 18

    Swiglo BA , Murad MH, Schünemann HJ, Kunz R, Vigersky RA, Guyatt GH, et al.. A case for clarity, consistency, and helpfulness: state-of-the-art clinical practice guidelines in endocrinology using the grading of recommendations, assessment, development, and evaluation system. J Clin Endocrinol Metab. 2008;93(3):66673.http://dx.doi.org/10.1210/jc.2007-1907.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 19

    Heilo A , Sigstad E, Fagerlid KH, Håskjold OI, Grøholt KK, Berner A, et al.. Efficacy of ultrasound-guided percutaneous ethanol injection treatment in patients with a limited number of metastatic cervical lymph nodes from papillary thyroid carcinoma. J Clin Endocrinol Metab. 2011 Sep;96(9):27505. http://dx.doi.org/10.1210/jc.2010-2952.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 20

    Hahn SY , Shin JH, Na DG, Ha EJ, Ahn HS, Lim HK, et al.. Ethanol ablation of the thyroid nodules: 2018 consensus statement by the Korean society of thyroid radiology. Korean J Radiol. 2019 Apr;20(4):60920.http://dx.doi.org/10.3348/kjr.2018.0696.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 21

    Jeong SY , Baek JH, Choi YJ, Lee JH. Ethanol and thermal ablation for malignant thyroid tumours. Int J Hyperthermia. 2017 Dec;33(8):93845. http://dx.doi.org/10.1080/02656736.2017.1361048.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 22

    Gharib H , Hegedüs L, Pacella CM, Baek JH, Papini E. Clinical review: nonsurgical, image-guided, minimally invasive therapy for thyroid nodules. J Clin Endocrinol Metab. 2013 Oct;98(10):394957.http://dx.doi.org/10.1210/jc.2013-1806.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 23

    Papini E , Pacella CM, Misischi I, Guglielmi R, Bizzarri G, Døssing H, et al.. The advent of ultrasound-guided ablation techniques in nodular thyroid disease: towards a patient-tailored approach. Best Pract Res Clin Endocrinol Metab. 2014;28(4):60118. http://dx.doi.org/10.1016/j.beem.2014.02.004.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 24

    Mauri G , Nicosia L, Della vigna P, Varano GM, Maiettini D, Bonomo G, et al.. Percutaneous laser ablation for benign and malignant thyroid diseases. Ultrasonography. 2019 Jan;38(1):2536. http://dx.doi.org/10.14366/usg.18034.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 25

    Mauri G , Cova L, Tondolo T, Ierace T, Baroli A, Di Mauro E, et al.. Percutaneous laser ablation of metastatic lymph nodes in the neck from papillary thyroid carcinoma: preliminary results. J Clin Endocrinol Metab. 2013 Jul;98(7):E12037.http://dx.doi.org/10.1210/jc.2013-1140.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 26

    Persichetti A , Bizzarri G, Guglielmi R, Barnabei A, Bianchini A, Coccaro C, et al.. Ultrasound-guided laser ablation for local control of neck recurrences of medullary thyroid cancer. A feasibility study. Int J Hyperthermia. 2018 Dec;35(1):48092. http://dx.doi.org/10.1080/02656736.2018.1508759.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 27

    Park HS , Baek JH, Park AW, Chung SR, Choi YJ, Lee JH. Thyroid radiofrequency ablation: updates on innovative devices and techniques. Korean J Radiol. 2017;18(4):61523.http://dx.doi.org/10.3348/kjr.2017.18.4.615.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 28

    Kim JH , Baek JH, Lim HK, Ahn HS, Baek SM, Choi YJ, et al.. 2017 Thyroid radiofrequency ablation guideline: Korean society of thyroid radiology. Korean J Radiol. 2018;19(4):63255.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 29

    Yue W , Chen L, Wang S, Yu S. Locoregional control of recurrent papillary thyroid carcinoma by ultrasound-guided percutaneous microwave ablation: a prospective study. Int J Hyperthermia. 2015 Jun;31(4):4038.http://dx.doi.org/10.3109/02656736.2015.1014433.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 30

    Teng D , Ding L, Wang Y, Liu C, Xia Y, Wang H. Safety and efficiency of ultrasound-guided low power microwave ablation in the treatment of cervical metastatic lymph node from papillary thyroid carcinoma: a mean of 32 months follow-up study. Endocrine. 2018 Dec;62(3):64854. http://dx.doi.org/10.1007/s12020-018-1711-4.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 31

    Cazzato RL , Garnon J, Ramamurthy N, Koch G, Tsoumakidou G, Caudrelier J, et al.. Percutaneous image-guided cryoablation: current applications and results in the oncologic field. Med Oncol. 2016;33(12):116. http://dx.doi.org/10.1007/s12032-016-0848-3.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 32

    Erinjeri JP , Clark TWI. Cryoablation: mechanism of action and devices. J Vasc Interv Radiol. 2010 Aug;21(Suppl 8):S187-91. http://dx.doi.org/10.1016/j.jvir.2009.12.403.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 33

    Inoue M , Nakatsuka S, Yashiro H, Ito N, Izumi Y, Yamauchi Y, et al.. Percutaneous cryoablation of lung tumors: feasibility and safety. J Vasc Interv Radiol. 2012 Mar;23(3):295305.http://dx.doi.org/10.1016/j.jvir.2011.11.019.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 34

    Cazzato RL , De Marini P, Leonard-Lorant I, Dalili D, Koch G, Autrusseau PA, et al.. Percutaneous thermal ablation of sacral metastases: assessment of pain relief and local tumor control. Diagn Interv Imaging. 2021 Apr;31(4):215360.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 35

    Chung SR , Baek JH, Choi YJ, Sung TY, Song DE, Kim TY, et al.. Efficacy of radiofrequency ablation for recurrent thyroid cancer invading the airways. Eur Radiol. 2020 Sep;18.http://dx.doi.org/10.1007/s00330-020-07283-w.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 36

    Orgera G , Monfardini L, Della Vigna P, Zhang L, Bonomo G, Arnone P, et al.. High-intensity focused ultrasound (HIFU) in patients with solid malignancies: evaluation of feasibility, local tumour response and clinical results. Radiol Med. 2011 Aug;116(5):73448.http://dx.doi.org/10.1007/s11547-011-0634-4.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 37

    Dietrich CF , Müller T, Bojunga J, Dong Y, Mauri G, Radzina M, et al.. Statement and recommendations on interventional ultrasound as a thyroid diagnostic and treatment procedure. Ultrasound Med Biol. 2018 Jan;44(1):1436. http://dx.doi.org/10.1016/j.ultrasmedbio.2017.08.1889.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 38

    Zhang M , Luo Y, Zhang Y, Tang J. Efficacy and safety of ultrasound-guided radiofrequency ablation for treating low-risk papillary thyroid microcarcinoma: a Prospective Study. Thyroid. 2016 Nov;26(11):15817.http://dx.doi.org/10.1089/thy.2015.0471.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 39

    Ding M , Tang X, Cui D, Chi J, Shi Y, Wang T, et al.. Clinical outcomes of ultrasound-guided radiofrequency ablation for the treatment of primary papillary thyroid microcarcinoma. Clin Radiol. 2019;74(9):7127. http://dx.doi.org/10.1016/j.crad.2019.05.012.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 40

    Lim HK , Cho SJ, Baek JH, Lee KD, Son CW, Son JM, et al.. US-guided radiofrequency ablation for low-risk papillary thyroid microcarcinoma: efficacy and safety in a large population. Korean J Radiol. 2019 Dec;20(12):165361.http://dx.doi.org/10.3348/kjr.2019.0192.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 41

    Tong M , Li S, Li YY, Li YY, Feng Y, Che Y. Efficacy and safety of radiofrequency, microwave and laser ablation for treating papillary thyroid microcarcinoma: a systematic review and meta-analysis. Int J Hyperthermia. 2019 Jan;36(1):127886. http://dx.doi.org/10.1080/02656736.2019.1700559.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 42

    Cho SJ , Baek SM, Lim HK, Lee KD, Son JM, Baek JH. Long-term follow-up results of ultrasound-guided radiofrequency ablation for low-risk papillary thyroid microcarcinoma: more than 5 year follow-up for 84 tumors. Thyroid. 2020 Dec;30(12):174551.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 43

    Cakir B , Topaloglu O, Gul K, Agac T, Aydin C, Dirikoc A, et al.. Ultrasound-guided percutaneous laser ablation treatment in inoperable aggressive course anaplastic thyroid carcinoma: the introduction of a novel alternative palliative therapy: second experience in the literature. J Endocrinol Invest. 2007;30(7):6245.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 44

    Jeong SY , Baek JH, Choi YJ, Chung SR, Sung TY, Kim WG, et al.. Radiofrequency ablation of primary thyroid carcinoma: efficacy according to the types of thyroid carcinoma. Int J Hyperthermia. 2018 Jul;34(5):6116. http://dx.doi.org/10.1080/02656736.2018.1427288.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 45

    Pacella CM , Bizzari G, Spiezia S, Bianchini A, Guglielmi R, Crescenzi A, et al.. Thyroid tissue: US-guided percutaneous laser thermal ablation. Radiology. 2004 Jul;232(1):27280.http://dx.doi.org/10.1148/radiol.2321021368.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 46

    Mauri G , Cova L, Ierace T, Baroli A, Di Mauro E, Pacella CM, et al.. Treatment of metastatic lymph nodes in the neck from papillary thyroid carcinoma with percutaneous laser ablation. Cardiovasc Intervent Radiol. 2016 Jul;39(7):102330. http://dx.doi.org/10.1007/s00270-016-1313-6.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 47

    Wang L , Ge M, Xu D, Chen L, Qian C, Shi K, et al.. Ultrasonography-guided percutaneous radiofrequency ablation for cervical lymph node metastasis from thyroid carcinoma. J Cancer Res Ther. 2014 Nov;10 Suppl:C1449.http://dx.doi.org/10.4103/0973-1482.145844.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 48

    Cazzato RL , Bonichon F, Buy X, Godbert Y, De Figuereido BH, Pointillart V, et al.. Over ten years of single-institution experience in percutaneous image-guided treatment of bone metastases from differentiated thyroid cancer. Eur J Surg Oncol. 2015 Sep;41(9):124755. http://dx.doi.org/10.1016/j.ejso.2015.06.005.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 49

    Bonichon F , Buy X, Godbert Y, Pointillart V, Henriques de Figueiredo B, Gangi A, et al.. Local treatment of metastases from differentiated thyroid cancer. Ann Endocrinol. 2015 Feb;76(1 Suppl 1):1S406.http://dx.doi.org/10.1016/S0003-4266(16)30013-0.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 50

    Zhang L , Zhou W, Zhan W, Peng Y, Jiang S, Xu S. Percutaneous laser ablation of unifocal papillary thyroid microcarcinoma: utility of conventional ultrasound and contrast-enhanced ultrasound in assessing local therapeutic response. World J Surg. 2018 Aug;42(8):247684. http://dx.doi.org/10.1007/s00268-018-4500-6.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 51

    Li J , Liu Y, Liu J, Qian L. Ultrasound-guided percutaneous microwave ablation versus surgery for papillary thyroid microcarcinoma. Int J Hyperthermia. 2018 Jul;34(5):6539. http://dx.doi.org/10.1080/02656736.2018.1453092.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 52

    Lan Y , Jin Z, Zhang Y, Song Q, Xiao J, Yan L, et al.. Factors associated with health-related quality of life in papillary thyroid microcarcinoma patients undergoing radiofrequency ablation: a cross-sectional prevalence study. Int J Hyperthermia. 2020 Jan;37(1):117481. http://dx.doi.org/10.1080/02656736.2020.1812738.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 53

    Wang L , Xu D, Yang Y, Li M, Zheng C, Qiu X, et al.. Safety and efficacy of ultrasound-guided percutaneous thermal ablation in treating low-risk papillary thyroid microcarcinoma: a pilot and feasibility study. J Cancer Res Ther. 2019 Oct;15(7):15229. http://dx.doi.org/10.4103/jcrt.JCRT_214_19.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 54

    Xiao J , Zhang Y, Zhang M, Lan Y, Yan L, Luo Y, et al.. Ultrasonography-guided radiofrequency ablation versus surgery for the treatment of solitary T1bN0M0 papillary thyroid carcinoma: a comparative study. Clin Endocrinol. 2021 Apr;94(4):68491.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 55

    Jeon MJ , Kim WG, Chung KW, Baek JH, Kim WB, Shong YK. Active surveillance of papillary thyroid microcarcinoma: where do we stand? Eur Thyroid J. 2019 Dec;8(6):298306. http://dx.doi.org/10.1159/000503064.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 56

    Kim HI , Jang HW, Ahn HS, Ahn S, Park SY, Oh YL, et al.. High serum TSH level is associated with progression of papillary thyroid microcarcinoma during active surveillance. J Clin Endocrinol Metab. 2018 Feb;103(2):44651.http://dx.doi.org/10.1210/jc.2017-01775.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 57

    Papini E , Guglielmi R, Gharib H, Misischi I, Graziano F, Chianelli M, et al.. Ultrasound-guided laser ablation of incidental papillary thyroid microcarcinoma: a potential therapeutic approach in patients at surgical risk. Thyroid. 2011;21(8):91720. http://dx.doi.org/10.1089/thy.2010.0447.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 58

    Zhang M , Tufano RP, Russell JO, Zhang Y, Zhang Y, Qiao Z, et al.. Ultrasound-guided radiofrequency ablation versus surgery for low-risk papillary thyroid microcarcinoma: results of over 5 years’ follow-up. Thyroid. 2020 Mar;30(3):40817.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 59

    Zhou W , Ni X, Xu S, Zhang L, Chen Y, Zhan W. Ultrasound-guided laser ablation versus surgery for solitary papillary thyroid microcarcinoma: a retrospective study. Int J Hyperthermia. 2019 Jan;36(1):897904. http://dx.doi.org/10.1080/02656736.2019.1649475.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 60

    Shen K , Xue S, Xie Y, Wang H, Li J, Sun Y, et al.. Comparison of thermal ablation and routine surgery for the treatment of papillary thyroid microcarcinoma: a systematic review and meta-analysis. Int J Hyperthermia. 2020 Jan;37(1):91324. http://dx.doi.org/10.1080/02656736.2020.1777331.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 61

    Guan SH , Wang H, Teng DK. Comparison of ultrasound-guided thermal ablation and conventional thyroidectomy for benign thyroid nodules: a systematic review and meta-analysis. Int J Hyperthermia. 2020 Jan;37(1):4429. http://dx.doi.org/10.1080/02656736.2020.1758802.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 62

    Hay ID , Lee RA, Kaggal S, Morris JC, Stan MN, Castro MR, et al.. Long-term results of treating with ethanol ablation 15 adult patients with cT1aN0 papillary thyroid microcarcinoma. J Endocr Soc. 2020;4(11):19. http://dx.doi.org/10.1210/jendso/bvaa135.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 63

    Kwon H , Oh H-S, Kim M, Park S, Jeon MJ, Kim WG, et al.. Active surveillance for patients with papillary thyroid microcarcinoma: a single center’s experience in Korea. J Clin Endocrinol Metab. 2017 Jun;102(6):191725.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 64

    Tuttle RM , Fagin JA, Minkowitz G, Wong RJ, Roman B, Patel S, et al.. Natural history and tumor volume kinetics of papillary thyroid cancers during active surveillance. JAMA Otolaryngol Head Neck Surg. 2017 Oct;143(10):101520. http://dx.doi.org/10.1001/jamaoto.2017.1442.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 65

    Oda H , Miyauchi A, Ito Y, Yoshioka K, Nakayama A, Sasai H, et al.. Incidences of unfavorable events in the management of low-risk papillary microcarcinoma of the thyroid by active surveillance versus immediate surgery. Thyroid. 2016 Jan;26(1):1505.http://dx.doi.org/10.1089/thy.2015.0313.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 66

    Park KW , Shin JH, Han BK, Ko EY, Chung JH. Inoperable symptomatic recurrent thyroid cancers: preliminary result of radiofrequency ablation. Ann Surg Oncol. 2011 Sep;18(9):25648. http://dx.doi.org/10.1245/s10434-011-1619-1.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 67

    Al-Salameh A , Baudry C, Gautier JF, Toubert ME, Bihan H, Cohen R. Late liver metastasis of medullary thyroid cancer with low calcitonin levels: successfully cured by radiofrequency. Endokrynol Pol. 2016;67(3):3269.http://dx.doi.org/10.5603/EP.a2016.0038.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 68

    Biamonte E , Solbiati L, Ierace T, Colombo P, Lavezzi E, Mazziotti G, et al.. Medullary thyroid carcinoma treated with percutaneous ultrasound-guided radiofrequency ablation. Endocrine. 2019 Sep;65(3):5159. http://dx.doi.org/10.1007/s12020-019-01995-w.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 69

    Ha SM , Sung JY, Baek JH, Na DG, Kim J-H, Yoo H, et al.. Radiofrequency ablation of small follicular neoplasms: initial clinical outcomes. Int J Hyperthermia. 2017 May;33(8):931.http://dx.doi.org/10.1080/02656736.2017.1331268.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 70

    Dobrinja C , Bernardi S, Fabris B, Eramo R, Makovac P, Bazzocchi G, et al.. Surgical and pathological changes after radiofrequency ablation of thyroid nodules. Int J Endocrinol. 2015;2015:576576. http://dx.doi.org/10.1155/2015/576576.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 71

    Schuff KG . Management of recurrent/persistent papillary thyroid carcinoma: efficacy of the surgical option. J Clin Endocrinol Metab. 2011 Jul;96(7):20389. http://dx.doi.org/10.1210/jc.2011-1663.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 72

    Lewis BD , Hay ID, Charboneau JW, McIver B, Reading CC, Goellner JR. Percutaneous ethanol injection for treatment of cervical lymph node metastases in patients with papillary thyroid carcinoma. AJR Am J Roentgenol. 2002 Mar;178(3):699704.http://dx.doi.org/10.2214/ajr.178.3.1780699.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 73

    Hay ID , Lee RA, Davidge-Pitts C, Reading CC, Charboneau JW. Long-term outcome of ultrasound-guided percutaneous ethanol ablation of selected “recurrent” neck nodal metastases in 25 patients with TNM stages III or IVA papillary thyroid carcinoma previously treated by surgery and 131I therapy. Surgery. 2013 Dec;154(6):14485. http://dx.doi.org/10.1016/j.surg.2013.07.007.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 74

    Guenette JP , Monchik JM, Dupuy DE. Image-guided ablation of postsurgical locoregional recurrence of biopsy-proven well-differentiated thyroid carcinoma. J Vasc Interv Radiol. 2013 May;24(5):6729.http://dx.doi.org/10.1016/j.jvir.2013.02.001.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 75

    Papini E , Bizzarri G, Bianchini A, Valle D, Misischi I, Guglielmi R, et al.. Percutaneous ultrasound-guided laser ablation is effective for treating selected nodal metastases in papillary thyroid cancer. J Clin Endocrinol Metab. 2013 Jan;98(1):E92-7. http://dx.doi.org/10.1210/jc.2012-2991.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 76

    Kim JH , Yoo WS, Park YJ, Park DJ, Yun TJ, Choi SH, et al.. Efficacy and safety of radiofrequency ablation for treatment of locally recurrent thyroid cancers smaller than 2 cm. Radiology. 2015 Sep;276(3):90918.http://dx.doi.org/10.1148/radiol.15140079.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 77

    Zhao Q , Tian G, Kong D, Jiang T. Meta-analysis of radiofrequency ablation for treating the local recurrence of thyroid cancers. J Endocrinol Invest. 2016 Aug;39(8):90916. http://dx.doi.org/10.1007/s40618-016-0450-8.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 78

    Suh CH , Baek JH, Choi YJ, Lee JH. Efficacy and safety of radiofrequency and ethanol ablation for treating locally recurrent thyroid cancer: a systematic review and meta-analysis. Thyroid. 2016 Mar;26(3):4208.http://dx.doi.org/10.1089/thy.2015.0545.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 79

    Choi Y , Jung SL, Bae JS, Lee SH, Jung CK, Jang J, et al.. Comparison of efficacy and complications between radiofrequency ablation and repeat surgery in the treatment of locally recurrent thyroid cancers: a single-center propensity score matching study. Int J Hyperthermia. 2019 Jan;36(1):35967. http://dx.doi.org/10.1080/02656736.2019.1571248.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 80

    De Baère T , Aupérin A, Deschamps F, Chevallier P, Gaubert Y, Boige V, et al.. Radiofrequency ablation is a valid treatment option for lung metastases: experience in 566 patients with 1037 metastases. Ann Oncol. 2015;26(5):98791.http://dx.doi.org/10.1093/annonc/mdv037.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 81

    Dupuy DE , Liu D, Hartfeil D, Hanna L, Blume JD, Ahrar K, et al.. Percutaneous radiofrequency ablation of painful osseous metastases: a multicenter American College of Radiology Imaging Network trial. Cancer. 2010 Feb 15;116(4):98997. http://dx.doi.org/10.1002/cncr.24837.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 82

    Callstrom MR , Dupuy DE, Solomon SB, Beres RA, Littrup PJ, Davis KW, et al.. Percutaneous image-guided cryoablation of painful metastases involving bone: multicenter trial. Cancer. 2013 Mar;119(5):103341.http://dx.doi.org/10.1002/cncr.27793.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 83

    Pacella CM , Di Stasio E, Guglielmi R, Baroli A, Pedrazzini L, Misischi I, et al.. Role of laser ablation in multimodal treatment of radioiodine- refractory bone metastases of thyroid cancer: a retrospective study. Endocrine. 2020 Nov;70(2):33847. http://dx.doi.org/10.1007/s12020-020-02314-4.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 84

    Auloge P , Cazzato RL, Rousseau C, Caudrelier J, Koch G, Rao P, et al.. Complications of percutaneous bone tumor cryoablation: a 10-year experience. Radiology. 2019 May;291(2):5218.http://dx.doi.org/10.1148/radiol.2019181262.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 85

    Luigi Cazzato R , Auloge P, De Marini P, Rousseau C, Chiang JB, Koch G, et al.. Percutaneous image-guided ablation of bone metastases: local tumor control in oligometastatic patients. Int J Hyperthermia. 2018 Dec;35(1):4939. http://dx.doi.org/10.1080/02656736.2018.1508760.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 86

    Cazzato RL , Garnon J, Caudrelier J, Rao PP, Koch G, Gangi A. Low-power bipolar radiofrequency ablation and vertebral augmentation for the palliative treatment of spinal malignancies. Int J Hyperthermia. 2018 Nov;34(8):12828. http://dx.doi.org/10.1080/02656736.2017.1422557.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 87

    Barat M , Tselikas L, de Baère T, Gravel G, Yevich S, Delpla A, et al.. Thermal-ablation of vertebral metastases prevents adverse events in patients with differentiated thyroid carcinoma. Eur J Radiol. 2019 Oct;119:108650. http://dx.doi.org/10.1016/j.ejrad.2019.108650.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 88

    Shyn PB , Mauri G, Alencar RO, Tatli S, Shah SH, Morrison PR, et al.. Percutaneous imaging-guided cryoablation of liver tumors: predicting local progression on 24-hour MRI. AJR Am J Roentgenol. 2014 Feb;203(2):W18191.http://dx.doi.org/10.2214/AJR.13.10747.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 89

    Han K , Kim JH, Yang SG, Park SH, Choi H-K, Chun S-Y, et al.. A single-center retrospective analysis of periprocedural variables affecting local tumor progression after radiofrequency ablation of colorectal cancer liver metastases. Radiology. 2021;298(1):2128.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 90

    Wertenbroek MWJLAE , Links TP, Prins TR, Plukker JTM, Van Der Jagt EJ, De Jong KP. Radiofrequency ablation of hepatic metastases from thyroid carcinoma. Thyroid. 2008 Oct;18(10):110510. http://dx.doi.org/10.1089/thy.2008.0080.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 91

    Yoon JH , Jeon MJ, Kim M, Ram Hong A, Kim HK, Shin DY, et al.. Unusual metastases from differentiated thyroid cancers: a multicenter study in Korea. PLoS One. 2020 Aug 25;15(8):e0238207. http://dx.doi.org/10.1371/journal.pone.0238207.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 92

    Hegedüs L , Frasoldati A, Negro R, Papini E. European thyroid association survey on use of minimally invasive techniques for thyroid nodules. Eur Thyroid J. 2020 Jul;9(4):194204. http://dx.doi.org/10.1159/000506513.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 93

    Papini E , Monpeyssen H, Frasoldati A, Hegedüs L. 2020 European thyroid association clinical practice guideline for the use of image-guided ablation in benign thyroid nodules. Eur Thyroid J. 2020 Jul;9(4):17285. http://dx.doi.org/10.1159/000508484.

    • PubMed
    • Search Google Scholar
    • Export Citation

Footnotes

Giovanni Mauri and Laszlo Hegedüs share first authorship.

 

  • Collapse
  • Expand
  • 1

    European Network of Cancer Registries Factsheets [Internet]. [cited 2021 Apr 7]. Available from: https://www.encr.eu/sites/default/files/factsheets/ENCR_Factsheet_Thyroid_2017-2.pdf.

    • PubMed
    • Export Citation
  • 2

    Figge JJ . Epidemiology of thyroid cancer. In: Thyroid cancer (second edition): a comprehensive guide to clinical management. Totowa, NJ: Humana Press; 2006. p. 913.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 3

    Durante C , Montesano T, Torlontano M, Attard M, Monzani F, Tumino S, et al.. Papillary thyroid cancer: time course of recurrences during postsurgery surveillance. J Clin Endocrinol Metab. 2013 Feb;98(2):63642.http://dx.doi.org/10.1210/jc.2012-3401.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 4

    Haugen BR , Alexander EK, Bible KC, Doherty GM, Mandel SJ, Nikiforov YE, et al.. 2015 American thyroid association management guidelines for adult patients with thyroid nodules and differentiated thyroid cancer: the American thyroid association guidelines task force on thyroid nodules and differentiated thyroid Cancer. Thyroid. 2016 Jan;26(1):1133.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 5

    Lim H , Devesa SS, Sosa JA, Check D, Kitahara CM. Trends in thyroid cancer incidence and mortality in the United States, 1974–2013. JAMA. 2017 Apr;317(13):133848.http://dx.doi.org/10.1001/jama.2017.2719.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 6

    Cho SJ , Baek JH, Chung SR, Choi YJ, Lee JH. Thermal ablation for small papillary thyroid cancer: a systematic review. Thyroid. 2019 Dec;29(12):177483. http://dx.doi.org/10.1089/thy.2019.0377.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 7

    Choi Y , Jung S-L. Efficacy and safety of thermal ablation techniques for the treatment of primary papillary thyroid microcarcinoma: a systematic review and meta-analysis. Thyroid. 2020 May;30(5):72031.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 8

    Mauri G , Orsi F, Carriero S, Della Vigna P, De Fiori E, Monzani D, et al.. Image-guided thermal ablation as an alternative to surgery for papillary thyroid microcarcinoma: preliminary results of an Italian experience. Front Endocrinol. 2021;11:575152.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 9

    Chereau N , Oyekunle TO, Zambeli-Ljepović A, Kazaure HS, Roman SA, Menegaux F, et al.. Predicting recurrence of papillary thyroid cancer using the eighth edition of the AJCC/UICC staging system. Br J Surg. 2019 Jun;106(7):88997. http://dx.doi.org/10.1002/bjs.11145.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 10

    Roti E , degli Uberti EC, Bondanelli M, Braverman LE. Thyroid papillary microcarcinoma: a descriptive and meta-analysis study. Eur J Endocrinol. 2008 Dec;159(6):65973.http://dx.doi.org/10.1530/EJE-07-0896.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 11

    Urken ML , Milas M, Randolph GW, Tufano R, Bergman D, Bernet V, et al.. Management of recurrent and persistent metastatic lymph nodes in well-differentiated thyroid cancer: a multifactorial decision-making guide for the thyroid cancer care collaborative. Head Neck. 2015 Apr;37(4):60514. http://dx.doi.org/10.1002/hed.23615.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 12

    Al-Saif O , Farrar WB, Bloomston M, Porter K, Ringel MD, Kloos RT. Long-term efficacy of lymph node reoperation for persistent papillary thyroid cancer. J Clin Endocrinol Metab. 2010;95(5):218794.http://dx.doi.org/10.1210/jc.2010-0063.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 13

    Mauri G , Gennaro N, Lee MK, Baek JH. Laser and radiofrequency ablations for benign and malignant thyroid tumors. Int J Hyperthermia. 2019 Oct;36(2):1320. http://dx.doi.org/10.1080/02656736.2019.1622795.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 14

    Durante C , Haddy N, Baudin E, Leboulleux S, Hartl D, Travagli JP, et al.. Long-term outcome of 444 patients with distant metastases from papillary and follicular thyroid carcinoma: benefits and limits of radioiodine therapy. J Clin Endocrinol Metab. 2006;91(8):28929.http://dx.doi.org/10.1210/jc.2005-2838.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 15

    Haugen BR , Alexander EK, Bible KC, Doherty GM, Mandel SJ, Nikiforov YE, et al.. 2015 American thyroid association management guidelines for adult patients with thyroid nodules and differentiated thyroid cancer: the American thyroid association guidelines task force on thyroid nodules and differentiated thyroid cancer. Thyroid. 2016 Jan;26(1):1133.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 16

    Filetti S , Durante C, Hartl D, Leboulleux S, Locati LD, Newbold K, et al.. Thyroid cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2019 Dec;30(12):185683.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 17

    Hegedüs L , Miyauchi A, Tuttle RM. Nonsurgical thermal ablation of thyroid nodules: not if, but why, when, and how? Thyroid. 2020 Dec;30(12):16914.

  • 18

    Swiglo BA , Murad MH, Schünemann HJ, Kunz R, Vigersky RA, Guyatt GH, et al.. A case for clarity, consistency, and helpfulness: state-of-the-art clinical practice guidelines in endocrinology using the grading of recommendations, assessment, development, and evaluation system. J Clin Endocrinol Metab. 2008;93(3):66673.http://dx.doi.org/10.1210/jc.2007-1907.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 19

    Heilo A , Sigstad E, Fagerlid KH, Håskjold OI, Grøholt KK, Berner A, et al.. Efficacy of ultrasound-guided percutaneous ethanol injection treatment in patients with a limited number of metastatic cervical lymph nodes from papillary thyroid carcinoma. J Clin Endocrinol Metab. 2011 Sep;96(9):27505. http://dx.doi.org/10.1210/jc.2010-2952.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 20

    Hahn SY , Shin JH, Na DG, Ha EJ, Ahn HS, Lim HK, et al.. Ethanol ablation of the thyroid nodules: 2018 consensus statement by the Korean society of thyroid radiology. Korean J Radiol. 2019 Apr;20(4):60920.http://dx.doi.org/10.3348/kjr.2018.0696.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 21

    Jeong SY , Baek JH, Choi YJ, Lee JH. Ethanol and thermal ablation for malignant thyroid tumours. Int J Hyperthermia. 2017 Dec;33(8):93845. http://dx.doi.org/10.1080/02656736.2017.1361048.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 22

    Gharib H , Hegedüs L, Pacella CM, Baek JH, Papini E. Clinical review: nonsurgical, image-guided, minimally invasive therapy for thyroid nodules. J Clin Endocrinol Metab. 2013 Oct;98(10):394957.http://dx.doi.org/10.1210/jc.2013-1806.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 23

    Papini E , Pacella CM, Misischi I, Guglielmi R, Bizzarri G, Døssing H, et al.. The advent of ultrasound-guided ablation techniques in nodular thyroid disease: towards a patient-tailored approach. Best Pract Res Clin Endocrinol Metab. 2014;28(4):60118. http://dx.doi.org/10.1016/j.beem.2014.02.004.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 24

    Mauri G , Nicosia L, Della vigna P, Varano GM, Maiettini D, Bonomo G, et al.. Percutaneous laser ablation for benign and malignant thyroid diseases. Ultrasonography. 2019 Jan;38(1):2536. http://dx.doi.org/10.14366/usg.18034.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 25

    Mauri G , Cova L, Tondolo T, Ierace T, Baroli A, Di Mauro E, et al.. Percutaneous laser ablation of metastatic lymph nodes in the neck from papillary thyroid carcinoma: preliminary results. J Clin Endocrinol Metab. 2013 Jul;98(7):E12037.http://dx.doi.org/10.1210/jc.2013-1140.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 26

    Persichetti A , Bizzarri G, Guglielmi R, Barnabei A, Bianchini A, Coccaro C, et al.. Ultrasound-guided laser ablation for local control of neck recurrences of medullary thyroid cancer. A feasibility study. Int J Hyperthermia. 2018 Dec;35(1):48092. http://dx.doi.org/10.1080/02656736.2018.1508759.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 27

    Park HS , Baek JH, Park AW, Chung SR, Choi YJ, Lee JH. Thyroid radiofrequency ablation: updates on innovative devices and techniques. Korean J Radiol. 2017;18(4):61523.http://dx.doi.org/10.3348/kjr.2017.18.4.615.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 28

    Kim JH , Baek JH, Lim HK, Ahn HS, Baek SM, Choi YJ, et al.. 2017 Thyroid radiofrequency ablation guideline: Korean society of thyroid radiology. Korean J Radiol. 2018;19(4):63255.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 29

    Yue W , Chen L, Wang S, Yu S. Locoregional control of recurrent papillary thyroid carcinoma by ultrasound-guided percutaneous microwave ablation: a prospective study. Int J Hyperthermia. 2015 Jun;31(4):4038.http://dx.doi.org/10.3109/02656736.2015.1014433.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 30

    Teng D , Ding L, Wang Y, Liu C, Xia Y, Wang H. Safety and efficiency of ultrasound-guided low power microwave ablation in the treatment of cervical metastatic lymph node from papillary thyroid carcinoma: a mean of 32 months follow-up study. Endocrine. 2018 Dec;62(3):64854. http://dx.doi.org/10.1007/s12020-018-1711-4.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 31

    Cazzato RL , Garnon J, Ramamurthy N, Koch G, Tsoumakidou G, Caudrelier J, et al.. Percutaneous image-guided cryoablation: current applications and results in the oncologic field. Med Oncol. 2016;33(12):116. http://dx.doi.org/10.1007/s12032-016-0848-3.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 32

    Erinjeri JP , Clark TWI. Cryoablation: mechanism of action and devices. J Vasc Interv Radiol. 2010 Aug;21(Suppl 8):S187-91. http://dx.doi.org/10.1016/j.jvir.2009.12.403.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 33

    Inoue M , Nakatsuka S, Yashiro H, Ito N, Izumi Y, Yamauchi Y, et al.. Percutaneous cryoablation of lung tumors: feasibility and safety. J Vasc Interv Radiol. 2012 Mar;23(3):295305.http://dx.doi.org/10.1016/j.jvir.2011.11.019.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 34

    Cazzato RL , De Marini P, Leonard-Lorant I, Dalili D, Koch G, Autrusseau PA, et al.. Percutaneous thermal ablation of sacral metastases: assessment of pain relief and local tumor control. Diagn Interv Imaging. 2021 Apr;31(4):215360.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 35

    Chung SR , Baek JH, Choi YJ, Sung TY, Song DE, Kim TY, et al.. Efficacy of radiofrequency ablation for recurrent thyroid cancer invading the airways. Eur Radiol. 2020 Sep;18.http://dx.doi.org/10.1007/s00330-020-07283-w.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 36

    Orgera G , Monfardini L, Della Vigna P, Zhang L, Bonomo G, Arnone P, et al.. High-intensity focused ultrasound (HIFU) in patients with solid malignancies: evaluation of feasibility, local tumour response and clinical results. Radiol Med. 2011 Aug;116(5):73448.http://dx.doi.org/10.1007/s11547-011-0634-4.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 37

    Dietrich CF , Müller T, Bojunga J, Dong Y, Mauri G, Radzina M, et al.. Statement and recommendations on interventional ultrasound as a thyroid diagnostic and treatment procedure. Ultrasound Med Biol. 2018 Jan;44(1):1436. http://dx.doi.org/10.1016/j.ultrasmedbio.2017.08.1889.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 38

    Zhang M , Luo Y, Zhang Y, Tang J. Efficacy and safety of ultrasound-guided radiofrequency ablation for treating low-risk papillary thyroid microcarcinoma: a Prospective Study. Thyroid. 2016 Nov;26(11):15817.http://dx.doi.org/10.1089/thy.2015.0471.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 39

    Ding M , Tang X, Cui D, Chi J, Shi Y, Wang T, et al.. Clinical outcomes of ultrasound-guided radiofrequency ablation for the treatment of primary papillary thyroid microcarcinoma. Clin Radiol. 2019;74(9):7127. http://dx.doi.org/10.1016/j.crad.2019.05.012.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 40

    Lim HK , Cho SJ, Baek JH, Lee KD, Son CW, Son JM, et al.. US-guided radiofrequency ablation for low-risk papillary thyroid microcarcinoma: efficacy and safety in a large population. Korean J Radiol. 2019 Dec;20(12):165361.http://dx.doi.org/10.3348/kjr.2019.0192.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 41

    Tong M , Li S, Li YY, Li YY, Feng Y, Che Y. Efficacy and safety of radiofrequency, microwave and laser ablation for treating papillary thyroid microcarcinoma: a systematic review and meta-analysis. Int J Hyperthermia. 2019 Jan;36(1):127886. http://dx.doi.org/10.1080/02656736.2019.1700559.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 42

    Cho SJ , Baek SM, Lim HK, Lee KD, Son JM, Baek JH. Long-term follow-up results of ultrasound-guided radiofrequency ablation for low-risk papillary thyroid microcarcinoma: more than 5 year follow-up for 84 tumors. Thyroid. 2020 Dec;30(12):174551.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 43

    Cakir B , Topaloglu O, Gul K, Agac T, Aydin C, Dirikoc A, et al.. Ultrasound-guided percutaneous laser ablation treatment in inoperable aggressive course anaplastic thyroid carcinoma: the introduction of a novel alternative palliative therapy: second experience in the literature. J Endocrinol Invest. 2007;30(7):6245.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 44

    Jeong SY , Baek JH, Choi YJ, Chung SR, Sung TY, Kim WG, et al.. Radiofrequency ablation of primary thyroid carcinoma: efficacy according to the types of thyroid carcinoma. Int J Hyperthermia. 2018 Jul;34(5):6116. http://dx.doi.org/10.1080/02656736.2018.1427288.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 45

    Pacella CM , Bizzari G, Spiezia S, Bianchini A, Guglielmi R, Crescenzi A, et al.. Thyroid tissue: US-guided percutaneous laser thermal ablation. Radiology. 2004 Jul;232(1):27280.http://dx.doi.org/10.1148/radiol.2321021368.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 46

    Mauri G , Cova L, Ierace T, Baroli A, Di Mauro E, Pacella CM, et al.. Treatment of metastatic lymph nodes in the neck from papillary thyroid carcinoma with percutaneous laser ablation. Cardiovasc Intervent Radiol. 2016 Jul;39(7):102330. http://dx.doi.org/10.1007/s00270-016-1313-6.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 47

    Wang L , Ge M, Xu D, Chen L, Qian C, Shi K, et al.. Ultrasonography-guided percutaneous radiofrequency ablation for cervical lymph node metastasis from thyroid carcinoma. J Cancer Res Ther. 2014 Nov;10 Suppl:C1449.http://dx.doi.org/10.4103/0973-1482.145844.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 48

    Cazzato RL , Bonichon F, Buy X, Godbert Y, De Figuereido BH, Pointillart V, et al.. Over ten years of single-institution experience in percutaneous image-guided treatment of bone metastases from differentiated thyroid cancer. Eur J Surg Oncol. 2015 Sep;41(9):124755. http://dx.doi.org/10.1016/j.ejso.2015.06.005.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 49

    Bonichon F , Buy X, Godbert Y, Pointillart V, Henriques de Figueiredo B, Gangi A, et al.. Local treatment of metastases from differentiated thyroid cancer. Ann Endocrinol. 2015 Feb;76(1 Suppl 1):1S406.http://dx.doi.org/10.1016/S0003-4266(16)30013-0.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 50

    Zhang L , Zhou W, Zhan W, Peng Y, Jiang S, Xu S. Percutaneous laser ablation of unifocal papillary thyroid microcarcinoma: utility of conventional ultrasound and contrast-enhanced ultrasound in assessing local therapeutic response. World J Surg. 2018 Aug;42(8):247684. http://dx.doi.org/10.1007/s00268-018-4500-6.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 51

    Li J , Liu Y, Liu J, Qian L. Ultrasound-guided percutaneous microwave ablation versus surgery for papillary thyroid microcarcinoma. Int J Hyperthermia. 2018 Jul;34(5):6539. http://dx.doi.org/10.1080/02656736.2018.1453092.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 52

    Lan Y , Jin Z, Zhang Y, Song Q, Xiao J, Yan L, et al.. Factors associated with health-related quality of life in papillary thyroid microcarcinoma patients undergoing radiofrequency ablation: a cross-sectional prevalence study. Int J Hyperthermia. 2020 Jan;37(1):117481. http://dx.doi.org/10.1080/02656736.2020.1812738.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 53

    Wang L , Xu D, Yang Y, Li M, Zheng C, Qiu X, et al.. Safety and efficacy of ultrasound-guided percutaneous thermal ablation in treating low-risk papillary thyroid microcarcinoma: a pilot and feasibility study. J Cancer Res Ther. 2019 Oct;15(7):15229. http://dx.doi.org/10.4103/jcrt.JCRT_214_19.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 54

    Xiao J , Zhang Y, Zhang M, Lan Y, Yan L, Luo Y, et al.. Ultrasonography-guided radiofrequency ablation versus surgery for the treatment of solitary T1bN0M0 papillary thyroid carcinoma: a comparative study. Clin Endocrinol. 2021 Apr;94(4):68491.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 55

    Jeon MJ , Kim WG, Chung KW, Baek JH, Kim WB, Shong YK. Active surveillance of papillary thyroid microcarcinoma: where do we stand? Eur Thyroid J. 2019 Dec;8(6):298306. http://dx.doi.org/10.1159/000503064.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 56

    Kim HI , Jang HW, Ahn HS, Ahn S, Park SY, Oh YL, et al.. High serum TSH level is associated with progression of papillary thyroid microcarcinoma during active surveillance. J Clin Endocrinol Metab. 2018 Feb;103(2):44651.http://dx.doi.org/10.1210/jc.2017-01775.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 57

    Papini E , Guglielmi R, Gharib H, Misischi I, Graziano F, Chianelli M, et al.. Ultrasound-guided laser ablation of incidental papillary thyroid microcarcinoma: a potential therapeutic approach in patients at surgical risk. Thyroid. 2011;21(8):91720. http://dx.doi.org/10.1089/thy.2010.0447.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 58

    Zhang M , Tufano RP, Russell JO, Zhang Y, Zhang Y, Qiao Z, et al.. Ultrasound-guided radiofrequency ablation versus surgery for low-risk papillary thyroid microcarcinoma: results of over 5 years’ follow-up. Thyroid. 2020 Mar;30(3):40817.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 59

    Zhou W , Ni X, Xu S, Zhang L, Chen Y, Zhan W. Ultrasound-guided laser ablation versus surgery for solitary papillary thyroid microcarcinoma: a retrospective study. Int J Hyperthermia. 2019 Jan;36(1):897904. http://dx.doi.org/10.1080/02656736.2019.1649475.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 60

    Shen K , Xue S, Xie Y, Wang H, Li J, Sun Y, et al.. Comparison of thermal ablation and routine surgery for the treatment of papillary thyroid microcarcinoma: a systematic review and meta-analysis. Int J Hyperthermia. 2020 Jan;37(1):91324. http://dx.doi.org/10.1080/02656736.2020.1777331.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 61

    Guan SH , Wang H, Teng DK. Comparison of ultrasound-guided thermal ablation and conventional thyroidectomy for benign thyroid nodules: a systematic review and meta-analysis. Int J Hyperthermia. 2020 Jan;37(1):4429. http://dx.doi.org/10.1080/02656736.2020.1758802.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 62

    Hay ID , Lee RA, Kaggal S, Morris JC, Stan MN, Castro MR, et al.. Long-term results of treating with ethanol ablation 15 adult patients with cT1aN0 papillary thyroid microcarcinoma. J Endocr Soc. 2020;4(11):19. http://dx.doi.org/10.1210/jendso/bvaa135.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 63

    Kwon H , Oh H-S, Kim M, Park S, Jeon MJ, Kim WG, et al.. Active surveillance for patients with papillary thyroid microcarcinoma: a single center’s experience in Korea. J Clin Endocrinol Metab. 2017 Jun;102(6):191725.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 64

    Tuttle RM , Fagin JA, Minkowitz G, Wong RJ, Roman B, Patel S, et al.. Natural history and tumor volume kinetics of papillary thyroid cancers during active surveillance. JAMA Otolaryngol Head Neck Surg. 2017 Oct;143(10):101520. http://dx.doi.org/10.1001/jamaoto.2017.1442.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 65

    Oda H , Miyauchi A, Ito Y, Yoshioka K, Nakayama A, Sasai H, et al.. Incidences of unfavorable events in the management of low-risk papillary microcarcinoma of the thyroid by active surveillance versus immediate surgery. Thyroid. 2016 Jan;26(1):1505.http://dx.doi.org/10.1089/thy.2015.0313.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 66

    Park KW , Shin JH, Han BK, Ko EY, Chung JH. Inoperable symptomatic recurrent thyroid cancers: preliminary result of radiofrequency ablation. Ann Surg Oncol. 2011 Sep;18(9):25648. http://dx.doi.org/10.1245/s10434-011-1619-1.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 67

    Al-Salameh A , Baudry C, Gautier JF, Toubert ME, Bihan H, Cohen R. Late liver metastasis of medullary thyroid cancer with low calcitonin levels: successfully cured by radiofrequency. Endokrynol Pol. 2016;67(3):3269.http://dx.doi.org/10.5603/EP.a2016.0038.

    • PubMed
    • Search Google Scholar
    • Export Citation