Tumour mutational burden as a biomarker for immunotherapy: Current data and emerging concepts.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
05 2020
Historique:
received: 20 12 2019
accepted: 13 02 2020
pubmed: 13 4 2020
medline: 28 10 2020
entrez: 13 4 2020
Statut: ppublish

Résumé

Treatment with immune checkpoint inhibitors targeting programmed cell death protein 1 (PD-1) or its ligand (PD-L1) can generate durable responses in various cancer types, but only in a subset of patients. The use of predictive biomarkers for response to PD-1/PD-L1 inhibitors is critical for patient selection. Expression of PD-L1 has demonstrated utility in patient selection. Tumour mutational burden (TMB) is an emerging biomarker for response to PD-1/PD-L1 inhibitors. The evaluation of this biomarker is based on the hypothesis that a high number of mutations in somatic exonic regions will lead to an increase in neoantigen production, which could then be recognised by CD8

Identifiants

pubmed: 32278982
pii: S0959-8049(20)30112-X
doi: 10.1016/j.ejca.2020.02.038
pmc: PMC9473693
mid: NIHMS1835439
pii:
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
B7-H1 Antigen 0
Biomarkers, Tumor 0
CD274 protein, human 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

40-50

Subventions

Organisme : NCI NIH HHS
ID : P50 CA062924
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

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Auteurs

Jean-David Fumet (JD)

Department of Medical Oncology, Center GF Leclerc, Dijon, France; Research Platform in Biological Oncology, Dijon, France; GIMI Genetic and Immunology Medical Institute, Dijon, France; University of Burgundy-Franche Comté, Dijon, France; UMR INSERM 1231, Dijon, France.

Caroline Truntzer (C)

Research Platform in Biological Oncology, Dijon, France; GIMI Genetic and Immunology Medical Institute, Dijon, France; UMR INSERM 1231, Dijon, France.

Mark Yarchoan (M)

Bloomberg-Kimmel Institute for Cancer Immunotherapy, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Francois Ghiringhelli (F)

Department of Medical Oncology, Center GF Leclerc, Dijon, France; Research Platform in Biological Oncology, Dijon, France; GIMI Genetic and Immunology Medical Institute, Dijon, France; University of Burgundy-Franche Comté, Dijon, France; UMR INSERM 1231, Dijon, France. Electronic address: fghiringhelli@cgfl.fr.

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Classifications MeSH