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西妥昔单抗联合 FOLFOX6 或 FOLFIRI 方案治疗转移性结直肠癌:CECOG 试验。

Cetuximab plus FOLFOX6 or FOLFIRI in metastatic colorectal cancer: CECOG trial.

机构信息

Institute of Oncology, 1000 Ljubljana, Slovenia.

出版信息

World J Gastroenterol. 2010 Jul 7;16(25):3133-43. doi: 10.3748/wjg.v16.i25.3133.

Abstract

AIM

To investigate efficacy and safety of cetuximab combined with two chemotherapy regimens in patients with unresectable metastatic colorectal cancer (mCRC).

METHODS

Randomized patients received cetuximab with 5-fluorouracil (5-FU), folinic acid (FA) and oxaliplatin (FOLFOX) 6 (arm A, n = 74) or 5-FU, FA and irinotecan (FOLFIRI) (arm B, n = 77). KRAS mutation status was determined retrospectively in a subset of tumors (n = 117).

RESULTS

No significant difference was found between treatment arms A and B in the progression-free survival (PFS) rate at 9 mo, 45% vs 34%; median PFS, 8.6 mo vs 8.3 mo [hazard ratio (HR) = 1.06]; overall response rate (ORR) 43% vs 45% [odds ratio (OR) = 0.93] and median overall survival (OS), 17.4 mo vs 18.9 mo (HR = 0.98). Patients with KRAS wild-type tumors demonstrated improved PFS (HR = 0.55, P = 0.0051), OS, (HR = 0.62, P = 0.0296) and ORR (53% vs 36%) and in arm A, improved PFS (HR = 0.49, P = 0.0196), OS (HR = 0.48, P = 0.0201) and ORR (56% vs 30%), compared with patients with KRAS mutated tumors. In arm B no significant differences were found in efficacy by KRAS mutation status. Treatment in arms A and B was generally well tolerated.

CONCLUSION

This study confirms that combinations of cetuximab with FOLFOX6 or FOLFIRI are effective and significantly improve clinical outcome in KRAS wild-type compared with KRAS mutated mCRC.

摘要

目的

研究西妥昔单抗联合两种化疗方案治疗不可切除转移性结直肠癌(mCRC)的疗效和安全性。

方法

将随机分组的患者分别接受西妥昔单抗联合氟尿嘧啶(5-FU)、亚叶酸(FA)和奥沙利铂(FOLFOX)6(A 组,n = 74)或 5-FU、FA 和伊立替康(FOLFIRI)(B 组,n = 77)治疗。在部分肿瘤(n = 117)中回顾性检测 KRAS 突变状态。

结果

A、B 两组 9 个月时无进展生存率(PFS)率、中位 PFS、总缓解率(ORR)和中位总生存期(OS)均无显著差异,分别为 45%比 34%、8.6 个月比 8.3 个月、43%比 45%和 17.4 个月比 18.9 个月[风险比(HR)=1.06];93%比 96%和 17.4 个月比 18.9 个月(HR = 0.98)。KRAS 野生型肿瘤患者的 PFS(HR = 0.55,P = 0.0051)、OS(HR = 0.62,P = 0.0296)和 ORR(53%比 36%)均得到改善,A 组患者的 PFS(HR = 0.49,P = 0.0196)、OS(HR = 0.48,P = 0.0201)和 ORR(56%比 30%)也得到改善,而 KRAS 突变型肿瘤患者则无显著差异。B 组患者的疗效与 KRAS 突变状态无关。A、B 两组的治疗均能较好耐受。

结论

本研究证实,西妥昔单抗联合 FOLFOX6 或 FOLFIRI 治疗方案在 KRAS 野生型 mCRC 中有效,与 KRAS 突变型 mCRC 相比,可显著改善临床结局。

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