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Tumor recurrence after thyroid surgery and thyroid hormone therapy with and without 131 I therapy. Total thyroidectomy includes subtotal thyroidectomy (ipsilateral lobectomy, isthmusectomy, and near-total contralateral lobectomy); subtotal thyroidectomy is lobectomy with or without isthmusectomy. Patients undergoing total thyroidectomy had more advanced tumor stage than those undergoing subtotal thyroidectomy (ANOVA, P 0.001). (Mazzaferri, E. L., unpublished data.) 

Tumor recurrence after thyroid surgery and thyroid hormone therapy with and without 131 I therapy. Total thyroidectomy includes subtotal thyroidectomy (ipsilateral lobectomy, isthmusectomy, and near-total contralateral lobectomy); subtotal thyroidectomy is lobectomy with or without isthmusectomy. Patients undergoing total thyroidectomy had more advanced tumor stage than those undergoing subtotal thyroidectomy (ANOVA, P 0.001). (Mazzaferri, E. L., unpublished data.) 

Contexts in source publication

Context 1
... lobectomy alone may result in a 5-10% recur- rence rate in the opposite thyroid lobe (27,28), a high tumor recurrence rate (Fig. 2), and a high (11%) incidence of subse- quent pulmonary metastases (29). High recurrence rates in pa- tients with cervical lymph node metastases and multicentric tumors (3) also justify bilateral thyroidectomy and 131 I ablation. If lobectomy is performed, microscopic metastases in the con- tralateral lobe or found by 131 I imaging may ...
Context 2
... treatment with 131 I also obscures the thera-peutic influence of surgery (8). Patients in our study treated with total or near-total thyroidectomy plus 131 I ablation and l-thyroxine had significantly fewer recurrences and distant recurrences than those treated with any other combination, including total thyroidectomy and l-thyroxine (Fig. 2). Sur- gery and 131 I therapy had independent effects on recurrence and cancer mortality ( Table 2). After a median follow-up of 16.6 yr, surgery more extensive than lobectomy was an in- dependent variable that reduced the likelihood of cancer death by 50% ( Table ...
Context 3
... lung metastases may be seen only on the posttreatment WBS after remnant ablation (57, 58). Lastly, remnant ablation may destroy residual normal follicular cells destined to become malignant (59) and occult cancer that might recur years later (Figs. 2 and 3). ...

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Citations

... Although most DTC carry with indolent clinical course and show good prognosis, metastatic DTC could be fatal, with 10% of patients developing distant metastasis (9,10). Lung is the most common site for distant metastases in DTC, and lung metastases (LMs) has been reported accounting for 4% in adult DTC (11), with a higher risk in children and young adults, with an incidence rate up to 23% -25% (12,13). ...
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... In metastatic DTCs, high-dose I 131 can be associated with complete responses, albeit rarely (16). Most tumor responses following RAI therapy are transient, mixed and/or completely refractory (17)(18)(19). Mechanistically, this is due in part to the genomic alterations which induce thyroid oncogenesis as well as inhibit thyroid cancer differentiation leading to impaired expression of the sodium iodine symporter (NIS), decreased follicular iodine uptake, and poor response to I-131 therapy (13,(20)(21) Redifferentiation therapy (RDT) is a potential salvage therapeutic strategy for patients with advanced DTCs, but with limited efficacy data to date. Currently, much of RDT is off label with outcome data that is limited to small cohorts with marked differences in patient selection and treatment protocols as well as a lack of comparison in clinical outcomes between patients with and without restored RAI avidity following RDT (24). ...
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Objective: Redifferentiation therapy (RDT) can restore radioactive iodine (RAI) uptake in differentiated thyroid cancer (DTC) cells to enable salvage 131I therapy for previously RAI refractory (RAIR) disease. This study evaluated the clinical outcomes of patients who underwent RDT and identified clinicopathologic characteristics predictive of RAI restoration following RDT. Methods: This is a retrospective case series of 33 patients with response evaluation criteria in solid tumors (RECIST)-progressive metastatic RAIR-DTC who underwent RDT between 2017 and 2022 at the Mayo Clinic (Rochester, MN). All patients underwent genomic profiling and received MEK, RET or ALK inhibitors alone, or combination BRAF-MEK inhibitors for 4 weeks. At week 3, those with increased RAI avidity in metastatic foci received high-dose 131I therapy. Baseline and clinicopathologic outcomes were comprehensively reviewed. Results: Of the 33 patients, 57.6% had restored RAI uptake following RDT (Redifferentiated subgroup). 42.1% (8/19) with papillary thyroid cancers (PTC), 100% (4/4) with invasive encapsulated follicular variant PTCs (IEFV-PTCs), and 100% (7/7) with follicular thyroid cancers (FTC) redifferentiated. All (11/11) RAS mutant tumors redifferentiated compared with 38.9% (7/18) with BRAF mutant disease (6 PTC and 1 IEFV-PTC). 76.5% (13/17) of redifferentiated and 66.7% (8/12) of non-redifferentiated patients achieved a best overall RECIST response of stable disease (SD) or non-complete response/non-progressive disease. Both subgroups had a median 12% tumor shrinkage at 3 weeks on drug(s) alone. The redifferentiated subgroup, following high-dose 131I therapy, achieved an additional median 20% tumor reduction at 6 months after RDT. There were no statistically significant differences between both groups in progression free survival (PFS), time to initiation of systemic therapy, and time to any additional therapy. Of the entire cohort, 6.1% (2/33) experienced histologic transformation to anaplastic thyroid cancer, 15.1% (5/33) died, and all had redifferentiated following RDT and received 131I therapy. Conclusion: RDT has the potential to restore RAI avidity and induce RECIST responses following 131I therapy in select patients with RAIR-DTC, particularly those with RAS-driven "follicular" phenotypes. In patients with PTC, none of the evaluated clinical outcomes differed statistically between the redifferentiated and non-redifferentiated subgroups. Further studies are needed to better characterize the long-term survival and/or safety outcomes of high-dose RAI following RDT, particularly whether it could be associated with histologic anaplastic transformation.
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Simple Summary The incidence of thyroid cancer (TC) has increased greatly since the 1970s, mostly because of higher detection of the small forms of papillary thyroid cancer (PTC). Despite this main and popular opinion, an increase in the occurrence of the larger forms of TC has also been observed. Due to some noticed trends concerning TC incidence and behavior, the management of these neoplasms has also changed in recent years. “Cancer screening activity”, which is the most popular of the aforementioned events, might have increased the PTC number during the analyzed period. However, the observed increase in the occurrence of TC continued to a point in time where there was a slowdown and even a reversal. This phenomenon is still debated and worthy of further investigation. Abstract Because of ambiguous and widely debated observations concerning the incidence, trend, and management of TC, we performed this analysis. We drew attention to some events, such as “cancer screening activity”, introduction of noninvasive follicular neoplasm with papillary-like nuclear features (NIFTP) to TC types, possibility of papillary thyroid microcarcinoma (PTMC) active surveillance (AS), occurrence of personalized medicine in TC management, and, finally, COVID-19 pandemic time. Because of the opinion that all changes have been made mostly by PTC, we compared it to the remaining types of TC in terms of incidence, clinical and pathological characteristics, and treatment. We analyzed patients treated in a single surgical center in eastern Europe (Poland). The prevalence of TC significantly increased from 5.15% in 2008 to 13.84% in 2015, and then significantly decreased to 1.33% in 2022 when the COVID-19 pandemic lasted (p < 0.0001). A similar trend was observed for PTC, when the incidence significantly increased to 13.99% in 2015 and then decreased to 1.38% in 2022 (p < 0.0001). At that time, the NIFTP category was introduced, and observation of PTMC began. The prevalence of FTC and MTC also increased until 2015 and then decreased. Significant differences in age, types of surgery, necessity of reoperation, and pTNM between PTCs and other types of TCs were observed. The average age was significantly lower in PTC patients than in patients with the remaining types of TC (p < 0.0001). Four milestones, including NIFTP introduction, the possibility of PTMC AS, personalized cancer medicine, and the COVID-19 pandemic, may have influenced the general statistics of TC.
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Preprint
Full-text available
Because of ambiguous and widely debated observations concerning incidence trend and management of TC, we performed this analysis. We drew attention to some events, such as “cancer screening activity,” introduction of noninvasive follicular neoplasm with papillary-like nuclear features (NIFTP) to TC types, possibility of papillary thyroid microcarcinoma (PTMC) active surveillance (AS), occurrence of personalized medicine in TC management and finally COVID-19 pandemic time. Because of the opinion that all changes have been made mostly by PTC, we compared it to the rest of types of TC in terms of incidence, clinical and pathological characteristics and treatment. The prevalence of TC significantly increased from 5.15% in 2008 to 13.84% in 2015 and then significantly decreased to 1.33% in 2022 when the pandemic lasted (p<0.0001). A similar trend was observed for PTC, when the incidence significantly increased to 13.99% in 2015 and then decreased to 1.38% in 2022 (p<0.0001). At that time, the NIFTP category was introduced, and observation of PTMC began. The prevalence of FTC and MTC also increased until 2015 and then decreased. Significant differences in age, types of surgery, necessity of reoperation, pTNM, between PTCs and other types of TCs were observed. The average age was significantly lower in PTC patients than in patients with the remaining types of TC (p<0.0001). Four milestones, including NIFTP introduction, the possibility of PTMC AS, personalized cancer medicine and the COVID-19 pandemic, may have influenced the general statistics of TC.