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papillary thyroid carcinoma (PTC); (b) the diagnostic purpose due to the possibility to perform a post-RRA whole-body scan (ptWBS) to identify additional sites of disease not identified before the RRA [ 2 - 4 ]; and (c) the facilitator purpose because the
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-FDG PET/CT scans performed over 5 years in DTC patients with stimulated Tg levels >10 ng/ml or positive anti-Tg antibody (TgAb) and a negative 131 I NaI whole-body scan (WBS). Patients were classified based on their TNM stage and ATA risk categorization
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of recurrence. In January 2018, he received 150 mCi (5550 MBq) of 131 I for thyroid ablation with subsequent post- 131 I therapy whole-body scan(WBS) indicating RAI accumulation in the thyroid bed and a low-grade RAI accumulation within the lungs
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-Tg antibodies (anti-Tg Ab). Stimulated Tg was measured either on the day of RAI administration in the case of levothyroxine withdrawal, or on the peak 5th or 6th day after rhTSH stimulation. A posttherapeutic whole body scan combined with SPECT CT (single photon
Thyroid Diseases Center, Instituto Israelita de Ensino e Pesquisa Albert Einstein, Brazil
Department of Nuclear Medicine, Irmandade Santa Casa de Misericórdia de São Paulo, São Paulo, Brazil
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24U and sU), all patients were instructed to follow an RID (table 1 ) and undergo thyroid hormone withdrawal before having 131 I treatment or a whole-body scan. For the RID, the 306 patients were divided into 2 groups of 153 patients; the first
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NOVA Medical School, Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Lisbon, Portugal
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NOVA Medical School, Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Lisbon, Portugal
Unidade de Investigação em Patobiologia Molecular, Instituto Português de Oncologia de Lisboa, Lisbon, Portugal
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, radioactive iodine; WBS, whole-body scan. She received 100 mCi of radioactive iodine (RAI) with recombinant TSH. The stimulated Tg was 7.5 ng/mL and the post-RAI whole-body scan showed a moderate cervical residual uptake (as presented in Fig. 1
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as several examinations per patient [ 4 ], sometimes followed by FNA, resulting in high costs. In patients with macroscopically complete tumor resection who receive RAI, persistent locoregional disease is more commonly detected by posttherapy whole-body
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were started on T 4 4 days after RAI. Thyroid-stimulating hormone (TSH)-stimulated 131 I diagnostic whole-body scans (DxWBS) and measurement of Tg and Tg antibody (Tg-Ab) levels either following thyroid hormone withdrawal or recombinant TSH
Thyroid Diseases Center, Instituto Israelita de Ensino e Pesquisa Albert Einstein, São Paulo, Brazil
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measurements (Tg temporal trend), stimulated Tg levels or whole-body scan (WBS) uptake. Subjects and Methods Study Design We performed a prospective study at a single Brazilian thyroid disease center to evaluate the outcomes of low-risk thyroid
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Objective: The prognostic value of stimulated thyroglobulin (sTg) and Tg-related parameters prior to and immediately after radioactive iodine (RAI) administration was assessed in a cohort of patients presenting with differentiated thyroid cancer (DTC) as a predictor of recurrent or progressive structural disease. Methods: Clinical records of 180 DTC patients were retrospectively reviewed, and serum TSH, Tg, and Tg antibodies were recorded just before RAI administration (pre-) and at the time of whole body scanning (post-). Based on the results of initial staging and RAI scintigraphy, patients were divided into two groups: those who were considered to be structurally disease-free after thyroidectomy and RAI (group 1) and those who were not (group 2). Univariate analyses were performed for pre-Tg, ratioTg (post-Tg/pre-Tg), and other clinical and pathological markers for long-term outcome, as well as separate bivariate analyses focusing on pre-Tg to correct for possible confounders. Different pre-Tg cut-off values for predicting structural disease recurrence were assessed in a subgroup of patients in group 1 prepared with thyroid hormone withdrawal. Results: In group 1, (n = 166) male gender, higher T-stage and both Tg-related parameters proved to be significant risk factors for structural disease relapse. Of all candidate variables, only higher T-stage served to predict progressive structural disease in group 2 (n = 14). Subgroup analysis showed a negative predictive value of 91.67% for pre-Tg < 10 µg/L. Conclusion: The sTg value at the time of RAI administration may be helpful in predicting structural disease recurrence in patients with DTC.