Encorafenib Plus Cetuximab as a New Standard of Care for Previously Treated BRAF V600E–Mutant Metastatic Colorectal Cancer: Updated Survival Results and Subgroup Analyses from the BEACON Study

Author:

Tabernero Josep1,Grothey Axel2,Van Cutsem Eric3,Yaeger Rona4,Wasan Harpreet5,Yoshino Takayuki6,Desai Jayesh7,Ciardiello Fortunato8,Loupakis Fotios9,Hong Yong Sang10,Steeghs Neeltje11,Guren Tormod Kyrre12,Arkenau Hendrik-Tobias13,Garcia-Alfonso Pilar14,Elez Elena1,Gollerkeri Ashwin15,Maharry Kati15,Christy-Bittel Janna15,Kopetz Scott16

Affiliation:

1. Vall d’Hebron University Hospital (HUVH), Vall d’Hebron Institute of Oncology (VHIO), UVic-UCC, IOB-Quiron, Barcelona, Spain

2. West Cancer Center, OneOncology, Germantown, TN

3. University Hospitals Gasthuisberg Leuven and KU Leuven, Leuven, Belgium

4. Memorial Sloan-Kettering Cancer Center, New York, NY

5. Hammersmith Hospital, Department of Cancer Medicine, Imperial College London, London, United Kingdom

6. National Cancer Center Hospital East, Kashiwa, Japan

7. Royal Melbourne Hospital and Peter MacCallum Cancer Centre, Walter and Aliza Hall Institute, Parkville, Australia

8. University of Campania, Naples, Italy

9. Istituto Oncologico Veneto IOV-IRCCS, Padua, Italy

10. Asan Medical Center, Seoul, South Korea

11. Netherlands Cancer Institute, Amsterdam, the Netherlands

12. Oslo University Hospital, Oslo, Norway

13. Sarah Cannon Research Institute, UCL Cancer Institute, University College London, London, United Kingdom

14. Hospital Gregorio Maranon, Madrid, Spain

15. Pfizer, New York, NY

16. The University of Texas MD Anderson Cancer Center, Houston, TX

Abstract

PURPOSE BEACON CRC evaluated encorafenib plus cetuximab with or without binimetinib versus investigators' choice of irinotecan or FOLFIRI plus cetuximab in patients with BRAFV600E–mutant metastatic colorectal cancer (mCRC), after progression on 1-2 prior regimens. In the previously reported primary analysis, encorafenib, binimetinib plus cetuximab (ENCO/BINI/CETUX; triplet) and encorafenib plus cetuximab (ENCO/CETUX; doublet) regimens improved overall survival (OS) and objective response rate (ORR; by blinded central review) versus standard of care. The purpose of this analysis was to report updated efficacy and safety data. METHODS In this open-label, phase III trial, 665 patients with BRAF V600E–mutant mCRC were randomly assigned 1:1:1 to receive triplet, doublet, or control. Primary end points were OS and independently reviewed ORR comparing triplet to control. OS for doublet versus control was a key secondary end point. Updated analyses include 6 months of additional follow-up and ORR for all randomized patients. RESULTS Patients received triplet (n = 224), doublet (n = 220), or control (n = 221). Median OS was 9.3 months (95% CI, 8.2 to 10.8) for triplet and 5.9 months (95% CI, 5.1 to 7.1) for control (hazard ratio [HR], 0.60 [95% CI, 0.47 to 0.75]). Median OS for doublet was 9.3 months (95% CI, 8.0 to 11.3) (HR v control, 0.61 [95% CI, 0.48 to 0.77]). Confirmed ORR was 26.8% (95% CI, 21.1% to 33.1%) for triplet, 19.5% (95% CI, 14.5% to 25.4%) for doublet, and 1.8% (95% CI, 0.5% to 4.6%) for control. Adverse events were consistent with the prior primary analysis, with grade ≥ 3 adverse events in 65.8%, 57.4%, and 64.2% for triplet, doublet, and control, respectively. CONCLUSION In the BEACON CRC study, encorafenib plus cetuximab improved OS, ORR, and progression-free survival in previously treated patients in the metastatic setting compared with standard chemotherapy. Based on the primary and updated analyses, encorafenib plus cetuximab is a new standard care regimen for previously treated patients with BRAF V600E mCRC.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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