FOLFIRI 联合西妥昔单抗与 FOLFIRI 联合贝伐珠单抗一线治疗转移性结直肠癌患者:KRAS 突变肿瘤患者的随机德国 AIO 研究 KRK-0306 亚组分析。

FOLFIRI plus cetuximab versus FOLFIRI plus bevacizumab as first-line treatment for patients with metastatic colorectal cancer-subgroup analysis of patients with KRAS: mutated tumours in the randomised German AIO study KRK-0306.

机构信息

Department of Medicine III, University Hospital Grosshadern, University of Munich, Munich, Germany.

出版信息

Ann Oncol. 2012 Jul;23(7):1693-9. doi: 10.1093/annonc/mdr571. Epub 2012 Jan 4.

Abstract

BACKGROUND

The AIO KRK-0306 trial compares the efficacy of infusional 5-fluorouracil, folinic acid, irinotecan (FOLFIRI) plus cetuximab with FOLFIRI plus bevacizumab in first-line treatment of metastatic colorectal cancer (mCRC). In October 2008, an amendment terminated the inclusion of patients with KRAS-mutated tumours. This subgroup of patients is evaluated in the present analysis, while the study is ongoing for patients with KRAS wild-type tumours.

METHODS

Patients were randomly assigned to FOLFIRI (Tournigand regimen) every 2 weeks plus cetuximab (400 mg/m2 day 1, followed by 250 mg/m2 weekly=arm A) or bevacizumab (5 mg/kg every 2 weeks=arm B). Among 336 randomised patients, KRAS mutation was demonstrated in 100 assessable patients. The primary study end point was objective response rate (ORR).

RESULTS

ORR was 44% [95% confidence interval (CI) 29% to 59%] in arm A versus 48% (95% CI, 33% to 62%) in arm B. Progression-free survival was 7.5 versus 8.9 months (hazard ratio: 1.0) and overall survival was 22.7 versus 18.7 months (hazard ratio: 0.86) in arms A versus B, respectively.

CONCLUSIONS

This is the first head to head comparison of cetuximab versus bevacizumab in first-line treatment of mCRC. In the present evaluation of patients with KRAS-mutated tumours, neither strategy demonstrated a clearly superior outcome.

摘要

背景

AIO KRK-0306 试验比较了氟尿嘧啶、亚叶酸钙、伊立替康(FOLFIRI)联合西妥昔单抗与 FOLFIRI 联合贝伐珠单抗在转移性结直肠癌(mCRC)一线治疗中的疗效。2008 年 10 月,一项修正案终止了 KRAS 突变型肿瘤患者的入组。本分析评估了这一亚组患者,而对于 KRAS 野生型肿瘤患者,该研究仍在进行中。

方法

患者被随机分配至每 2 周接受 FOLFIRI(Tournigand 方案)联合西妥昔单抗(400mg/m2,第 1 天,随后每周 250mg/m2=A 组)或贝伐珠单抗(每 2 周 5mg/kg=B 组)治疗。在 336 名随机患者中,有 100 名可评估患者显示 KRAS 突变。主要研究终点为客观缓解率(ORR)。

结果

A 组的 ORR 为 44%(95%CI 29%至 59%),B 组为 48%(95%CI,33%至 62%)。A 组和 B 组的无进展生存期分别为 7.5 个月和 8.9 个月(风险比:1.0),总生存期分别为 22.7 个月和 18.7 个月(风险比:0.86)。

结论

这是西妥昔单抗与贝伐珠单抗在 mCRC 一线治疗中首次进行的头对头比较。在本研究对 KRAS 突变型肿瘤患者的评估中,两种策略均未显示出明显更优的结果。

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