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thyroid carcinomas (PTCs) to develop a homogeneous cohort ( Cancer Genome Atlas Research Network 2014 ). Limited data exist regarding the mutational profile in advanced thyroid cancers, such as poorly differentiated thyroid carcinomas (PDTCs), anaplastic
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. 2013 ). Until recently, no effective therapeutic options have been available for patients with any type of advanced thyroid cancer. In fact, EBRT has significant toxicity and mainly plays a palliative role, and classical cytotoxic chemotherapies have
Endocrinology Service, Human Oncology and Pathogenesis Program, Department of Pathology, Department of Medicine
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density of TAMs ( n =3) and tumors with a high density of TAMs ( n =3). Discussion Our study demonstrates, for the first time, that an increased density of TAMs is associated with tumor progression in advanced thyroid cancers. There is a remarkably strong
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, Yoo et al . 2019 ). Although BRAF and RAS were the predominant drivers in PDTC and ATC, TERT promoter mutations and TP53 were highly prevalence in advanced thyroid cancers harboring BRAF or RAS ( Landa et al . 2013 , Liu et al . 2013
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. ( doi:10.1158/1078-0432.CCR-10-0994 ). Cohen EE Rosen LS Vokes EE Kies MS Forastiere AA Worden FP Kane MA Sherman E Kim S Bycott P 2008 Axitinib is an active treatment for all histologic subtypes of advanced thyroid cancer
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.1089/thy.2012.0329 ) 23427907 10.1089/thy.2012.0329 Covell LL Ganti AK 2015 Treatment of advanced thyroid cancer: role of molecularly targeted therapies . Targeted Oncology 10 311 – 324 . ( https://doi.org/10.1007/s11523-014-0331-z ) 10.1007/s
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M Song E Ryu YM Song DE Kim SY Kim TY Kim WB Shong YK Jeon MJ 2021 Immune profiling of advanced thyroid cancers using fluorescent multiplex immunohistochemistry . Thyroid 31 61 – 67 . ( https://doi.org/10.1089/thy.2020
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PV/PV Pten +/− mice, SAHA is not only ineffective therapeutically but paradoxically promotes thyroid cancer progression. These observations are reminiscent of the outcome of the clinical trial of 19 patients with advanced thyroid cancer ( Woyach et
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and found higher expression in a subset of advanced thyroid cancers such as anaplastic thyroid carcinoma and follicular thyroid carcinoma. Identification of PD-L1 expression may have direct therapeutic relevance to patients with refractory thyroid
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events (AE) were considered. The authors concluded that sorafenib showed only a modest effect in patients with advanced thyroid cancer. I wonder if 70% of PR plus SD would be considered as a modest response to treatment of patients with advanced