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Encorafenib plus binimetinib in patients with BRAFV600-mutant non-small cell lung cancer: Phase II PHAROS study design

  • Gregory J. Riely
  • , Myung Ju Ahn
  • , Enriqueta Felip
  • , Suresh S. Ramalingam
  • , Egbert F. Smit
  • , Anne S. Tsao
  • , Ann Alcasid
  • , Tiziana Usari
  • , Paul S. Wissel
  • , Keith D. Wilner
  • , Bruce E. Johnson
  • Memorial Sloan-Kettering Cancer Center
  • Vall d'Hebron Institute of Oncology
  • Emory University
  • Netherlands Cancer Institute
  • University of Texas MD Anderson Cancer Center
  • Pfizer
  • Dana-Farber Cancer Institute

Research output: Contribution to journalReview articlepeer-review

Abstract

BRAFV600 oncogenic driver mutations occur in 1-2% of non-small-cell lung cancers (NSCLCs) and have been shown to be a clinically relevant target. Preclinical/clinical evidence support the efficacy and safety of BRAF and MEK inhibitor combinations in patients with NSCLC with these mutations. We describe the design of PHAROS, an ongoing, open-label, single-arm, phase II trial evaluating the BRAF inhibitor encorafenib plus the MEK inhibitor binimetinib in patients with metastatic BRAFV600-mutant NSCLC, as first- or second-line treatment. The primary end point is objective response rate, based on independent radiologic review (per RECIST v1.1); secondary objectives evaluated additional efficacy end points and safety. Results from PHAROS will describe the antitumor activity/safety of encorafenib plus binimetinib in patients with metastatic BRAFV600-mutant NSCLC.

Original languageEnglish
Pages (from-to)781-791
Number of pages11
JournalFuture Oncology
Volume18
Issue number7
DOIs
StatePublished - Mar 2022

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • BRAFmutation
  • binimetinib
  • clinical trial
  • efficacy
  • encorafenib
  • non-small-cell lung cancer
  • objective response rate
  • safety

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