安戈非尼、替尼美替尼和西妥昔单抗治疗 BRAFV600E 突变转移性结直肠癌的安全性和有效性:日本扩大准入计划的结果

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Daisuke Kotani , Atsuo Takashima , Takeshi Kato , Taroh Satoh , Toshiki Masuishi , Yoshito Komatsu , Manabu Shiozawa , Taito Esaki , Naoki Izawa , Shinji Takeuchi , Hideaki Bando , Satoru Iwasa , Hiroko Hasegawa , Toshifumi Yamaguchi , Hiroya Taniguchi , Yasunori Ushida , Toshiya Oizaki , Chiaki Inoue , Takayuki Yoshino
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引用次数: 0

摘要

BEACON CRC 3 期研究证明了安戈非尼和西妥昔单抗联合或不联合比尼替尼(BEACON 三联或双联方案)治疗突变转移性结直肠癌 (mCRC) 的生存获益。这项扩大准入计划(EAP)和后续随访研究评估了 BEACON 三联方案在日本-突变型 mCRC 患者中的疗效和安全性。EAP 是一项开放标签、单臂研究,研究对象包括既往接受过 1-2 种治疗方案后病情出现进展的日本突变型 mCRC 患者。患者接受了 BEACON 三联疗法,周期为 28 天。随后的随访研究评估了 EAP 完成后的生存结果。安全性仅在 EAP 期间进行评估。在 86 例入组患者中,81 例接受了 BEACON 三联疗法。客观反应率和中位无进展生存期分别为 27.6%(95% 置信区间 [CI],18.0%-39.1%)和 5.26(95% CI,4.14-5.52)个月。分别有43.2%和28.4%的患者发生了3-4级不良事件和治疗相关不良事件。EAP 期间未观察到新的安全性信号。在完成 EAP 时确认存活的 58 例患者中,有 57 例被纳入随访研究。EAP 和随访研究的中位观察期为 9.17 个月,中位总生存期为 10.38 个月(95% CI,9.00-16.16)。BEACON三联方案在日本的-突变mCRC患者中的疗效和安全性与BEACON CRC试验报告的结果一致,支持将其作为-突变mCRC预处理患者的标准治疗方案。安可非尼、西妥昔单抗和替米替尼(BEACON 三联方案)延长了-突变转移性结直肠癌(mCRC)患者的生存期,但其在日本患者中的疗效仍未确定。本研究评估了 BEACON 三联疗法在日本患者中的疗效和安全性。总体结果与之前的试验一致,支持将其作为-突变型 mCRC 患者的标准治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety and Efficacy of Encorafenib, Binimetinib, and Cetuximab for BRAFV600E-Mutant Metastatic Colorectal Cancer: Results of the Japanese Expanded Access Program

Background

The phase 3 BEACON CRC study demonstrated the survival benefits of encorafenib and cetuximab, with or without binimetinib (the BEACON triplet or doublet regimen), for BRAFV600E-mutant metastatic colorectal cancer (mCRC). This expanded access program (EAP) and subsequent follow-up study assessed the efficacy and safety of the BEACON triplet regimen in Japanese patients with BRAFV600E-mutant mCRC.

Materials and Methods

The EAP was an open-label, single-arm study including Japanese patients with BRAFV600E-mutant mCRC whose disease progressed after 1 to 2 prior regimens. The patients received the BEACON triplet regimen with 28-day cycles. The subsequent follow-up study assessed the survival outcomes following EAP completion. Safety was assessed only during the EAP.

Results

Among the 86 enrolled patients, 81 received the BEACON triplet regimen. The objective response rate and median progression-free survival were 27.6% (95% confidence interval [CI], 18.0%-39.1%) and 5.26 (95% CI, 4.14-5.52) months, respectively. Grade 3 to 4 adverse events and treatment-related adverse events occurred in 43.2% and 28.4% of patients, respectively. No new safety signals were observed during the EAP. Among 58 patients with confirmed survival at EAP completion, 57 were included in the follow-up study. With a median observation period of 9.17 months through the EAP and follow-up study, the median overall survival was 10.38 (95% CI, 9.00-16.16) months.

Conclusion

The efficacy and safety of the BEACON triplet regimen in Japanese patients with BRAFV600E-mutant mCRC were consistent with those reported in the BEACON CRC trial, supporting its use as a standard treatment for pretreated patients with BRAFV600E-mutant mCRC.

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