First report of a Japanese phase I study of triplet plus bevacizumab for chemotherapy-naive metastatic colorectal cancer (J1-TRIBE study)

Hironaga Satake, Akihito Tsuji, Takeshi Kotake, Yoshihiro Okita, Yukimasa Hatachi
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引用次数: 3

Abstract

Background

The aim of this study was to determine the recommended dose of irinotecan (CPT-11) with fixed regimen of oxaliplatin (L-OHP)/fluorouracil (5-FU)/leucovorin (LV) (FOLFOXIRI) plus bevacizumab in Japanese patients with metastatic colorectal cancer.

Patients and methods

Patients received CPT-11 followed by L-OHP 85 mg/m2, LV 200 mg/m2, and 5-FU 3200 mg/m2 infused as a 48-h continuous infusion and bevacizumab 5 mg/kg, repeated every 2 weeks. A decrease of the CPT-11 dose was planned (started at level 1: CPT-11 165 mg/m2). This trial was registered with the University Hospital Medical Information Network (number UMIN000012991).

Results

Six patients were enrolled, and MTD was not reached at level 1. CPT-11 165 mg/ in combination with L-OHP 85 mg/m2, LV 200 mg/m2, 5-FU 3200 mg/m2 infused as a 48-h continuous infusion and bevacizumab 5 mg/kg could be administered with acceptable toxicity, and all patients were treated at these dose levels. The most common grade 3 or 4 toxicities were neutropenia (67%) and leukopenia (50%). No treatment death was observed. The overall response rate was 67% (95% confidence interval: 30.0–90.3 %).

Conclusion

This biweekly triplet plus bevacizumab regimen was well tolerated by Japanese patients with metastatic colorectal cancer. The recommended phase II dose was determined to be the same as the standard doses for this regimen used worldwide.

Micro abstract

The efficacy of the FOLFOXIRI plus bevacizumab regimen for patients with metastatic colorectal cancer has been proven in a recent phase III study. However, there is no report of the FOLFOXIRI plus bevacizumab regimen in Japanese patients, and recommended doses of this regimen for Japanese patients have not been determined. The present study demonstrates that the recommended doses of FOLFOXIRI plus bevacizumab for Japanese patients are the same as the standard doses used worldwide.

日本一项triplet联合贝伐单抗治疗化疗初期转移性结直肠癌的I期研究(J1-TRIBE研究)的第一份报告
本研究的目的是确定伊立替康(CPT-11)与奥沙利铂(L-OHP)/氟尿嘧啶(5-FU)/亚叶酸钙(LV) (FOLFOXIRI)联合贝伐单抗治疗日本转移性结直肠癌患者的推荐剂量。患者和方法患者接受CPT-11后,L-OHP 85 mg/m2, LV 200 mg/m2, 5- fu 3200mg /m2连续输注48 h,贝伐单抗5 mg/kg,每2周重复一次。计划减少CPT-11剂量(从第1级开始:CPT-11 165 mg/m2)。本试验已在大学医院医学信息网注册(编号:UMIN000012991)。结果6例患者入组,MTD未达到1级。CPT-11 165 mg/ /联合L-OHP 85 mg/m2, LV 200 mg/m2, 5- fu 3200mg /m2连续输注48小时,贝伐单抗5 mg/kg,均可接受毒性,所有患者均在这些剂量水平下治疗。最常见的3级或4级毒性是中性粒细胞减少(67%)和白细胞减少(50%)。未观察到治疗死亡。总有效率为67%(95%置信区间:30.0 - 90.3%)。结论:日本转移性结直肠癌患者对这种双周三联用药加贝伐单抗的治疗方案耐受良好。推荐的II期剂量被确定为与该方案在世界范围内使用的标准剂量相同。最近的一项III期研究证实了FOLFOXIRI联合贝伐单抗治疗转移性结直肠癌患者的疗效。然而,在日本患者中没有FOLFOXIRI +贝伐单抗方案的报道,并且该方案对日本患者的推荐剂量尚未确定。目前的研究表明,日本患者的FOLFOXIRI加贝伐单抗的推荐剂量与世界范围内使用的标准剂量相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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