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Updated Overall Survival Analysis From the Phase II PHAROS Study of Encorafenib Plus Binimetinib in Patients With BRAF V600E-Mutant Metastatic Non-Small Cell Lung Cancer

  • Melissa L. Johnson
  • , Egbert F. Smit
  • , Enriqueta Felip
  • , Suresh S. Ramalingam
  • , Myung Ju Ahn
  • , Anne Tsao
  • , Bruce E. Johnson
  • , Michael Offin
  • , Maen Hussein
  • , Ibiayi Dagogo-Jack
  • , Jonathan W. Goldman
  • , Jeffrey M. Clarke
  • , Marcelo V. Negrao
  • , Rachel E. Sanborn
  • , Daniel Morgensztern
  • , Tiziana Usari
  • , Keith Wilner
  • , Linh Alejandro
  • , Nada Rifi
  • , Xiaosong Zhang
  • Gregory J. Riely
  • Sarah Cannon Research Institute
  • Leiden University
  • Vall d'Hebron Institute of Oncology
  • Emory University
  • University of Texas MD Anderson Cancer Center
  • Dana-Farber Cancer Institute
  • Memorial Sloan-Kettering Cancer Center
  • Florida Cancer Specialists and Research Institute
  • Massachusetts General Hospital Cancer Center
  • University of California at Los Angeles
  • Duke University
  • Providence Cancer Institute
  • Washington University St. Louis
  • Pfizer

Research output: Contribution to journalArticlepeer-review

Abstract

The phase II PHAROS study previously showed that encorafenib plus binimetinib has antitumor activity in patients with BRAF V600E-mutant metastatic non-small cell lung cancer (mNSCLC). In PHAROS, 98 patients (59 treatment-naïve; 39 previously treated) received encorafenib 450 mg once daily and binimetinib 45 mg twice daily. We report updated results from data cutoff of March 14, 2025. The median duration of treatment with both encorafenib and binimetinib was 16.3 months in treatment-naïve and 5.5 months in previously treated patients. After median follow-up for overall survival (OS) of 52.3 months in treatment-naïve patients, mOS was 47.6 months (95% CI, 31.3 to not estimable); 4-year OS probability was 49% (95% CI, 35 to 62). After median follow-up for OS of 48.2 months in previously treated patients, mOS was 22.7 months (95% CI, 14.1 to 32.6); 4-year OS probability was 31% (95% CI, 16 to 47). In treatment-naïve and previously treated groups, 58% and 26% received ≥1 subsequent systemic anticancer treatment, respectively. Safety profile remained consistent with that in previous analyses. Although comparisons across trials should be done cautiously, to our knowledge, encorafenib plus binimetinib was associated with the longest mOS reported to date with targeted treatment in patients with treatment-naïve BRAF V600E-mutant mNSCLC.

Original languageEnglish
Pages (from-to)3706-3713
Number of pages8
JournalJournal of Clinical Oncology
Volume43
Issue number35
DOIs
StatePublished - 10 Dec 2025

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

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