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Predictive factors of outcome in poorly differentiated thyroid carcinomas.
de la Fouchardière, Christelle; Decaussin-Petrucci, Myriam; Berthiller, Julien; Descotes, Françoise; Lopez, Jonathan; Lifante, Jean-Christophe; Peix, Jean-Louis; Giraudet, Anne-Laure; Delahaye, Armelle; Masson, Sandrine; Bournaud-Salinas, Claire; Borson Chazot, Françoise.
Afiliação
  • de la Fouchardière C; Medical Oncology Department, Centre Leon Berard, University Lyon I, Lyon, France. Electronic address: christelle.delafouchardiere@lyon.unicancer.fr.
  • Decaussin-Petrucci M; Pathology Department, Hospital Lyon-Sud, University Lyon I, Pierre-Bénite, France.
  • Berthiller J; Epidemiology, Pharmacology and Clinical Investigations, Mother Child Hospital, Bron; University Lyon I, Lyon, France.
  • Descotes F; Biochemistry and Molecular Biology Department, Hospital Lyon-Sud, University Lyon I, Lyon, Pierre-Bénite, France.
  • Lopez J; Biochemistry and Molecular Biology Department, Hospital Lyon-Sud, University Lyon I, Lyon, Pierre-Bénite, France.
  • Lifante JC; Department of General and Endocrine Surgery, University Hospital Lyon-Sud, Lyon, France.
  • Peix JL; Department of General and Endocrine Surgery, University Hospital Lyon-Sud, Lyon, France.
  • Giraudet AL; Department of Nuclear Medicine Centre Leon Berard, University Lyon I, Lyon, France.
  • Delahaye A; Endocrinology Department-INSERM, UMR 1052, University Lyon I, Lyon, France.
  • Masson S; Endocrinology Department-INSERM, UMR 1052, University Lyon I, Lyon, France.
  • Bournaud-Salinas C; Department of Nuclear Medicine, Hospital Louis Pradel, University Lyon I, Bron, France.
  • Borson Chazot F; Endocrinology Department-INSERM, UMR 1052, University Lyon I, Lyon, France.
Eur J Cancer ; 92: 40-47, 2018 03.
Article em En | MEDLINE | ID: mdl-29413688
ABSTRACT

BACKGROUND:

The prognosis of poorly differentiated thyroid carcinomas (PDTC) is heterogeneous though generally poor. The objectives of this study were to identify clinical and molecular factors of poor prognosis.

METHODS:

One hundred four consecutive patients treated for a PDTC between 01/01/2000 and 31/12/2010 were included in this study. A pathological review was done for all cases (blinded to clinical data and outcome).

RESULTS:

All patients underwent thyroidectomy. Adjuvant radioactive-iodine was administered in 95.2% of them. Tumours were pT3 or pT4 in 68.3% of cases and metastatic in 38.5% of patients. Extrathyroidal extension (ETE) was observed in 40% of patients. At the end of the initial treatment, only 37% of patients were considered in remission. Fifty-two patients (50%) became refractory to radioiodine during follow-up. The 5-year overall survival was 72.8% and the 5-year recurrence-free survival (RFS) was 45.3%. Remission after initial treatment was an independent factor of RFS (HR = 0.22; [0.10-0.49]). ETE was the only significant parameter influencing the overall survival in multivariate analysis. TERT promoter mutations at positions -124 (C228T) and -146 (C250T) were present in 38.1% of analysed patients and significantly associated with radioiodine resistance but not with overall survival. Half of TERT promoter mutant tumours harboured also RAS or BRAF mutations.

CONCLUSION:

PDTC form a heterogeneous group of patients with usual late-stage diagnosis, low radioactive iodine avidity and frequent metastatic spread. TERT promoter mutations could help to identify patients with high risk of radio-iodine refractoriness.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tireoidectomia / Neoplasias da Glândula Tireoide / Carcinoma / Diferenciação Celular Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies País/Região como assunto: Europa Idioma: En Revista: Eur J Cancer Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tireoidectomia / Neoplasias da Glândula Tireoide / Carcinoma / Diferenciação Celular Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies País/Região como assunto: Europa Idioma: En Revista: Eur J Cancer Ano de publicação: 2018 Tipo de documento: Article