A multicenter phase II trial of encorafenib, binimetinib, and cetuximab for early relapsed stage II/III <i>BRAF</i> <sup>V600E</sup> -mutated colorectal cancer: TRESBIEN trial (OGSG 2101).

3567 Background: Patients with BRAF V600E -mutated colorectal cancer (CRC) who experience early recurrence during or shortly after adjuvant therapy show an extremely poor prognosis. The efficacy of BRAF-targeted triplet therapy for early relapse remains unclear. Methods: We conducted a prospective, open-label, multicenter, phase II trial evaluating the efficacy and safety of encorafenib, binimetinib and cetuximab in BRAF V600E -mutated CRC patients who relapsed during or within 6 months after completing adjuvant chemotherapy. Patients received encorafenib 300 mg once daily and binimetinib 45 mg twice daily in 28-day cycles, plus intravenous cetuximab 400 mg/m 2 once on day 1 of cycle 1, then 250 mg/m 2 once weekly until disease progression or occurrence of unacceptable adverse events. The primary endpoint was objective response rate (ORR) by blinded independent central review. Secondary endpoints were overall survival (OS), progression-free survival (PFS), disease control rate (DCR), and safety. Sample size was determined based on a threshold ORR of 6.0% and an expected ORR of 26.0% (one-sided α = 0.05, power = 0.90). Results: Between January 2022 and April 2025, 25 patients were enrolled across 14 institutions. Baseline characteristics included: median age 68 years (range, 28–81); female, n = 18 (72.0%); right-sided, n = 18 (72.0%); pStage II/III, n = 2 (8.0%)/23 (92.0%); MSI-H, n = 5 (20.0%); and prior oxaliplatin-based adjuvant chemotherapy, n = 22 (88.0%). Twenty-four patients were evaluable for efficacy. The ORR was 62.5% (95% CI, 40.6–81.2, one-sided P &lt; 0.001), and DCR was 87.5% (95% CI, 67.6–97.3). With median follow-up time of 18.0 months, the median PFS was 7.4 months (95% CI, 4.7–10.6), and the median OS was 33.9 months (95% CI, 11.0–NE). No Grade ≥3 adverse events (≥10%) and treatment-related deaths were observed. Conclusions: The combination of encorafenib, binimetinib, and cetuximab demonstrated favorable efficacy and a manageable safety profile in patients with BRAF V600E -mutated CRC who relapsed early recurrence during or shortly after adjuvant chemotherapy. This triplet regimen can be a promising treatment strategy for this poor prognostic population. Clinical trial information: jRCTs051210152.

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Publication Details

Journal
Journal of Clinical Oncology
Published
2026-05-27
DOI
https://doi.org/10.1200/jco.2026.44.16_suppl.3567
Primary Topic
Colorectal Cancer Treatments and Studies
Type
article
Field-Weighted Citation Impact
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article

A multicenter phase II trial of encorafenib, binimetinib, and cetuximab for early relapsed stage II/III BRAF V600E -mutated colorectal cancer: TRESBIEN trial (OGSG 2101).

Chiaki Inagaki, Koichi Okuya, Toshifumi Yamaguchi, Masayoshi Nakanishi et al.
Journal of Clinical Oncology
Colorectal Cancer Treatments and Studies
article

A multicenter phase II trial of encorafenib, binimetinib, and cetuximab for early relapsed stage II/III BRAF V600E -mutated colorectal cancer: TRESBIEN trial (OGSG 2101).

Chiaki Inagaki, Koichi Okuya, Toshifumi Yamaguchi, Masayoshi Nakanishi, Shingo Noura, Toshihiro Kudo, Yoshinori Kagawa, Narikazu Boku, Yusuke Suwa, Ichiro Takemasa, Atsushi Naito, Taroh Satoh, Hiroyuki Okuda, Hironaga Satake, Yukinori Kurokawa, Mitsuyoshi Tei, Shogen Boku, Osaka Gastrointestinal Cancer Chemotherapy Study Group: OGSG, Takashi Ohta, Toshio Shimokawa
article en

Abstract

3567 Background: Patients with BRAF V600E -mutated colorectal cancer (CRC) who experience early recurrence during or shortly after adjuvant therapy show an extremely poor prognosis. The efficacy of BRAF-targeted triplet therapy for early relapse remains unclear. Methods: We conducted a prospective, open-label, multicenter, phase II trial evaluating the efficacy and safety of encorafenib, binimetinib and cetuximab in BRAF V600E -mutated CRC patients who relapsed during or within 6 months after completing adjuvant chemotherapy. Patients received encorafenib 300 mg once daily and binimetinib 45 mg twice daily in 28-day cycles, plus intravenous cetuximab 400 mg/m 2 once on day 1 of cycle 1, then 250 mg/m 2 once weekly until disease progression or occurrence of unacceptable adverse events. The primary endpoint was objective response rate (ORR) by blinded independent central review. Secondary endpoints were overall survival (OS), progression-free survival (PFS), disease control rate (DCR), and safety. Sample size was determined based on a threshold ORR of 6.0% and an expected ORR of 26.0% (one-sided α = 0.05, power = 0.90). Results: Between January 2022 and April 2025, 25 patients were enrolled across 14 institutions. Baseline characteristics included: median age 68 years (range, 28–81); female, n = 18 (72.0%); right-sided, n = 18 (72.0%); pStage II/III, n = 2 (8.0%)/23 (92.0%); MSI-H, n = 5 (20.0%); and prior oxaliplatin-based adjuvant chemotherapy, n = 22 (88.0%). Twenty-four patients were evaluable for efficacy. The ORR was 62.5% (95% CI, 40.6–81.2, one-sided P &lt; 0.001), and DCR was 87.5% (95% CI, 67.6–97.3). With median follow-up time of 18.0 months, the median PFS was 7.4 months (95% CI, 4.7–10.6), and the median OS was 33.9 months (95% CI, 11.0–NE). No Grade ≥3 adverse events (≥10%) and treatment-related deaths were observed. Conclusions: The combination of encorafenib, binimetinib, and cetuximab demonstrated favorable efficacy and a manageable safety profile in patients with BRAF V600E -mutated CRC who relapsed early recurrence during or shortly after adjuvant chemotherapy. This triplet regimen can be a promising treatment strategy for this poor prognostic population. Clinical trial information: jRCTs051210152.

Journal of Clinical OncologyVol. 44(16_suppl)
Osaka Gakuin University (JP), Kansai Medical University (JP), Panasonic (Japan) (JP), Sapporo Medical University (JP), Tokyo Medical University (JP), Wakayama Medical University (JP), Yokohama City University Medical Center (JP), Kochi Medical School Hospital (JP), Sakai Municipal Hospital (JP), Osaka Rosai Hospital (JP), Kansai Rosai Hospital (JP), Kindai University Sakai Hospital (JP), Osaka Hospital (JP), Keiyukai Sapporo Hospital (JP), Matsushita Memorial Hospital (JP), Osaka International Cancer Institute (JP), Osaka University Hospital (JP), Yokohama City University (JP), Osaka University of Pharmaceutical Sciences (JP), The University of Osaka (JP)
Ono Pharmaceutical
No poverty
Openalex Percentile: Top 12%
Colorectal Cancer Treatments and Studies
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