TERT promoter mutations and melanoma survival: A comprehensive literature review and meta-analysis.

Melanoma Meta-analysis Review Survival Telomerase reverse transcriptase gene promoter

Journal

Critical reviews in oncology/hematology
ISSN: 1879-0461
Titre abrégé: Crit Rev Oncol Hematol
Pays: Netherlands
ID NLM: 8916049

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 23 01 2020
revised: 02 01 2021
accepted: 27 02 2021
pubmed: 7 3 2021
medline: 21 4 2021
entrez: 6 3 2021
Statut: ppublish

Résumé

We conducted a systematic review and meta-analysis of the association between somatic mutations of the TERT gene promoter and melanoma survival. Data from nineteen independent studies (>2,500 melanoma overall) were pooled using random effects meta-analysis models. TERT-mutated melanoma patients had a significantly worse overall survival (OS) (summary hazard ratio 1.43, 95 % confidence intervals (CI) 1.05-1.95) compared to wild-type ones. The association became stronger when combining risk estimates for overall and melanoma-specific survival (MSS) (1.52, 95 % CI 1.14-2.02), and when restricting the analysis to studies mostly based on invasive non-acral cutaneous melanomas (1.77, 95 % CI 1.00-3.15). Limited, yet suggestive evidence of a detrimental effect of TERT promoter mutations on melanoma prognosis emerged also for other survival measures (e.g. disease-free and distant metastasis-free survival). We found suggestive evidence of a detrimental effect of TERT mutations on melanoma patients' survival.

Identifiants

pubmed: 33675908
pii: S1040-8428(21)00076-7
doi: 10.1016/j.critrevonc.2021.103288
pii:
doi:

Substances chimiques

TERT protein, human EC 2.7.7.49
Telomerase EC 2.7.7.49

Types de publication

Journal Article Meta-Analysis Review Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

103288

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Sara Gandini (S)

Department of Experimental Oncology, European Institute of Oncology (IEO), IRCCS, Milan, Italy.

Ines Zanna (I)

Cancer Risk Factors and Lifestyle Epidemiology Unit, Institute for Cancer Research, Prevention and Clinical Network (ISPRO), Florence, Italy.

Simone De Angelis (S)

Department of Experimental Oncology, European Institute of Oncology (IEO), IRCCS, Milan, Italy.

Domenico Palli (D)

Cancer Risk Factors and Lifestyle Epidemiology Unit, Institute for Cancer Research, Prevention and Clinical Network (ISPRO), Florence, Italy.

Sara Raimondi (S)

Department of Experimental Oncology, European Institute of Oncology (IEO), IRCCS, Milan, Italy.

Simone Ribero (S)

Department of Medical Sciences, Dermatology Clinic, University of Turin, Italy.

Giovanna Masala (G)

Cancer Risk Factors and Lifestyle Epidemiology Unit, Institute for Cancer Research, Prevention and Clinical Network (ISPRO), Florence, Italy.

Mariano Suppa (M)

Department of Dermatology, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.

Federica Bellerba (F)

Department of Experimental Oncology, European Institute of Oncology (IEO), IRCCS, Milan, Italy.

Federica Corso (F)

Department of Experimental Oncology, European Institute of Oncology (IEO), IRCCS, Milan, Italy.

Luigi Nezi (L)

Department of Experimental Oncology, European Institute of Oncology (IEO), IRCCS, Milan, Italy.

Eduardo Nagore (E)

Department of Dermatology, Instituto Valenciano de Oncología, Valencia, Spain.

Saverio Caini (S)

Cancer Risk Factors and Lifestyle Epidemiology Unit, Institute for Cancer Research, Prevention and Clinical Network (ISPRO), Florence, Italy. Electronic address: s.caini@ispro.toscana.it.

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Classifications MeSH