Encorafenib, Binimetinib, and Cetuximab in BRAF V600E-Mutated Colorectal Cancer.


Journal

Translational oncology
ISSN: 1936-5233
Titre abrégé: Transl Oncol
Pays: United States
ID NLM: 101472619

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 20 02 2020
revised: 28 04 2020
accepted: 30 04 2020
pubmed: 30 5 2020
medline: 30 5 2020
entrez: 30 5 2020
Statut: ppublish

Résumé

BRAFV600-mutated colorectal cancer (CRC) accounts for 8% to 12% of all CRC diagnoses. These tumors are often associated with specific patient features, including right-sided primary tumor location, peritoneal and non-regional lymph node involvement, and poor prognosis. In approximately 30% of cases, a simultaneous mismatch repair deficient (dMMR)/microsatellite instability-high (MSI-H) phenotype is identified. The prognostic impact of the BRAF mutation appears to be less marked in patients with MSI-H CRC than in patients with microsatellite stable (MSS) tumor. The treatment of BRAFV600-mutated CRC is still a challenge for the clinicians, mainly due to the poor survival outcomes obtained with traditional chemotherapy regimens. In recent years, two novel treatment strategies have offered remarkable changes in the treatment of this specific patient subgroup. The first approach has included targeted therapies directed against BRAF and MEK, with support from the epidermal growth factor receptor (EGFR) blockade. The second approach has included immunotherapeutic agents that have been shown to be particularly promising for patients with simultaneous dMMR/MSI-H phenotype. Here we review the clinical trials that specifically enrolled patients with BRAF-mutated CRC, from the phase I/II studies to the phase III trial BEACON CRC. We also examine the future directions towards a molecularly guided therapy for patients with BRAF-mutated CRC and the crucial role of a molecularly and clinically based algorithm in order to offer the best choice of treatment for these patients.

Identifiants

pubmed: 32470910
pii: S1936-5233(20)30205-9
doi: 10.1016/j.tranon.2020.100795
pmc: PMC7260582
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

100795

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that there are no conflicts of interest.

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Auteurs

Giandomenico Roviello (G)

Department of Health Sciences, University of Florence, viale Pieraccini, 6, 50139, Florence, Italy. Electronic address: giandomenicoroviello@hotmail.it.

Alberto D'Angelo (A)

Department of Biology and Biochemistry, University of Bath, Bath BA2 7AY, United Kingdom.

Roberto Petrioli (R)

Medical Oncology Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena, Italy.

Franco Roviello (F)

Unit of General Surgery and Surgical Oncology, Department of Medicine, Surgery and Neurosciences, University of Siena, Viale Bracci - Policlinico "Le Scotte", 53100, Siena, Italy.

Fabio Cianchi (F)

Department of Experimental and Clinical Medicine, University of Florence, Largo Brambilla 3, 50134, Florence, Italy.

Stefania Nobili (S)

Department of Health Sciences, University of Florence, viale Pieraccini, 6, 50139, Florence, Italy.

Enrico Mini (E)

Department of Health Sciences, University of Florence, viale Pieraccini, 6, 50139, Florence, Italy.

Daniele Lavacchi (D)

Azienda Ospedaliera Careggi University Hospital of Florence and University of Florence, 50134 Florence, Italy.

Classifications MeSH