TERT Promoter Mutations Are a Major Indicator of Poor Outcome in Differentiated Thyroid Carcinomas

• Tipo: Artigo em Revista Científica Internacional
• Data: 2014

Autores

Miguel Melo (Autor) Outra; Adriana Gaspar da Rocha (Autor) Outra; Joao Vinagre (Autor) Outra; Rui Batista (Autor) Outra; Joana Peixoto (Autor) Outra; Catarina Tavares (Autor) Outra; Ricardo Celestino (Autor) Outra; Ana Almeida (Autor) Outra; Catarina Salgado (Autor) Outra; Catarina Eloy (Autor) Outra; Patricia Castro (Autor) Outra; Hugo Prazeres (Autor) Outra; Jorge Lima (Autor) FMUP; Teresina Amaro (Autor) Outra; Claudia Lobo (Autor) Outra; Maria Joao Martins (Autor) Outra; Margarida Moura (Autor) Outra; Branca Cavaco (Autor) Outra; Valeriano Leite (Autor) Outra; Jose Manuel Cameselle Teijeiro (Autor) Outra; Francisco Carrilho (Autor) Outra; Manuela Carvalheiro (Autor) Outra; Valdemar Maximo (Autor) Outra; Manuel Sobrinho Simoes (Autor) Outra; Paula Soares (Autor) FMUP

Revista

Título: Journal of Clinical Endocrinology and Metabolism

Vol. 99

Páginas: E754-E765

ISSN: 0021-972X

Editora: Endocrine Society

Indexação

ISI Web of Knowledge - 408 Citações

Scopus - 444 Citações

Classificação Científica

FOS: Ciências médicas e da saúde > Medicina clínica

Outras Informações

ID Authenticus: P-009-DWN

DOI: 10.1210/jc.2013-3734

Abstract (EN): Context: Telomerase promoter mutations (TERT) were recently described in follicular cell-derived thyroid carcinomas (FCDTC) and seem to be more prevalent in aggressive cancers. Objectives: We aimed to evaluate the frequency of TERT promoter mutations in thyroid lesions and to investigate the prognostic significance of such mutations in a large cohort of patients with differentiated thyroid carcinomas (DTCs). Design: This was a retrospective observational study. Setting and Patients: We studied 647 tumors and tumor-like lesions. A total of 469 patients with FCDTC treated and followed in five university hospitals were included. Mean follow-up (+/- SD) was 7.8 +/- 5.8 years. Main Outcome Measures: Predictive value of TERT promoter mutations for distant metastasization, disease persistence at the end of follow-up, and disease-specific mortality. Results: TERT promoter mutations were found in 7.5% of papillary carcinomas (PTCs), 17.1% of follicular carcinomas, 29.0% of poorly differentiated carcinomas, and 33.3% of anaplastic thyroid carcinomas. Patients with TERT-mutated tumors were older (P < .001) and had larger tumors (P = .002). In DTCs, TERT promoter mutations were significantly associated with distant metastases (P < .001) and higher stage (P < .001). Patients with DTC harboring TERT promoter mutations were submitted to more radioiodine treatments (P = .009) with higher cumulative dose (P = .004) and to more treatment modalities (P = .001). At the end of follow-up, patients with TERT-mutated DTCs were more prone to have persistent disease (P = .001). TERT promoter mutations were significantly associated with disease-specific mortality [in the whole FCDTC (P < .001)] in DTCs (P < .001), PTCs (P = .001), and follicular carcinomas (P < .001). After adjusting for age at diagnosis and gender, the hazard ratio was 10.35 (95% confidence interval 2.01-53.24; P = .005) in DTC and 23.81 (95% confidence interval 1.36-415.76; P = .03) in PTCs. Conclusions: TERT promoter mutations are an indicator of clinically aggressive tumors, being correlated with worse outcome and disease-specific mortality in DTC. TERT promoter mutations have an independent prognostic value in DTC and, notably, in PTC.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 12