Acquired BRAF inhibitor resistance: A multicenter meta-analysis of the spectrum and frequencies, clinical behaviour, and phenotypic associations of resistance mechanisms.

Abstract

BACKGROUND:

Acquired resistance to BRAF inhibitors (BRAFi) is a near-universal phenomenon caused by numerous genetic and non-genetic alterations. In this study, we evaluated the spectrum, onset, pattern of progression, and subsequent clinical outcomes associated with specific mechanisms of resistance.

METHODS:

We compiled clinical and genetic data from 100 patients with 132 tissue samples obtained at progression on BRAFi therapy from 3 large, previously published studies of BRAFi resistance. These samples were subjected to whole-exome sequencing and/or polymerase chain reaction-based genetic testing.

RESULTS:

Among 132 samples, putative resistance mechanisms were identified in 58%, including NRAS or KRAS mutations (20%), BRAF splice variants (16%), BRAF(V600E/K) amplifications (13%), MEK1/2 mutations (7%), and non-mitogen-activated protein kinase pathway alterations (11%). Marked heterogeneity was observed within tumors and patients; 18 of 19 patients (95%) with more than one progression biopsy had distinct/unknown drivers of resistance between samples. NRAS mutations were associated with vemurafenib use (p = 0.045) and intracranial metastases (p = 0.036), and MEK1/2 mutations correlated with hepatic progression (p = 0.011). Progression-free survival and overall survival were similar across resistance mechanisms. The median survival after disease progression was 6.9 months, and responses to subsequent BRAF and MEK inhibition were uncommon (2 of 15; 13%). Post-progression outcomes did not correlate with specific acquired BRAFi-resistance mechanisms.

CONCLUSIONS:

This is the first study to systematically characterise the clinical implications of particular acquired BRAFi-resistance mechanisms in patients with BRAF-mutant melanoma largest study to compile the landscape of resistance. Despite marked heterogeneity of resistance mechanisms within patients, NRAS mutations correlated with vemurafenib use and intracranial disease involvement.

• Authors: Douglas B Johnson, Alexander M Menzies, Lisa Zimmer, Zeynep Eroglu, Fei Ye, Shilin Zhao, Helen Rizos, Antje Sucker, Richard A Scolyer, Ralf Gutzmer, Helen Gogas, Richard F Kefford, John F Thompson, Jürgen C Becker, Carola Berking, Friederike Egberts, Carmen Loquai, Simone M Goldinger, Gulietta M Pupo, Willy Hugo, Xiangju Kong, Levi A Garraway, Jeffrey A Sosman, Antoni Ribas, Roger S Lo, Georgina V Long, Dirk Schadendorf
• Journal: European journal of cancer (Oxford, England : 1990) (Eur J Cancer) Vol. 51 Issue 18 Pg. 2792-9 (Dec 2015) ISSN: 1879-0852 [Electronic] England
• PMID: 26608120 (Publication Type: Journal Article, Meta-Analysis, Multicenter Study, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2015 Elsevier Ltd. All rights reserved.

Chemical References

• Antineoplastic Agents
• Biomarkers, Tumor
• Protein Kinase Inhibitors
• BRAF protein, human
• Proto-Oncogene Proteins B-raf

Topics

• Antineoplastic Agents (therapeutic use)
• Australia
• Biomarkers, Tumor (antagonists & inhibitors, genetics, metabolism)
• DNA Mutational Analysis
• Disease Progression
• Disease-Free Survival
• Drug Resistance, Neoplasm (genetics)
• Europe
• Female
• Genetic Predisposition to Disease
• Humans
• Kaplan-Meier Estimate
• Male
• Melanoma (drug therapy, enzymology, genetics, mortality, pathology)
• Middle Aged
• Mutation
• Phenotype
• Proportional Hazards Models
• Protein Kinase Inhibitors (therapeutic use)
• Proto-Oncogene Proteins B-raf (antagonists & inhibitors, genetics, metabolism)
• Risk Factors
• Signal Transduction (drug effects)
• Skin Neoplasms (drug therapy, enzymology, genetics, mortality, pathology)
• Time Factors
• Treatment Outcome
• United States