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首页> 外文期刊>Investigational new drugs. >Phase II study of combination chemotherapy with irinotecan and cetuximab for pretreated metastatic colorectal cancer harboring wild-type KRAS.
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Phase II study of combination chemotherapy with irinotecan and cetuximab for pretreated metastatic colorectal cancer harboring wild-type KRAS.

机译:伊立替康和西妥昔单抗联合化疗联合治疗携带野生型KRAS的转移性结直肠癌的II期研究。

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The aim of this study was to prospectively evaluate the efficacy of combination irinotecan and cetuximab chemotherapy in patients with pretreated metastatic colorectal cancer harboring wild-type KRAS. Patients with metastatic colorectal cancer that had progressed after chemotherapy with irinotecan, oxaliplatin, and fluoropyrimidine were included. KRAS status was evaluated using the Cycleave PCR method; only patients without KRAS mutations were included. Cetuximab was administered initially at 400 mg/m(2) followed by weekly 250 mg/m(2) infusions. Irinotecan was administered biweekly. From October 2008 to April 2009, a total of 30 patients were enrolled. The objective response rate was 30.0% (95% confidence interval [CI], 14.7-49.4%) and the disease control rate (complete response, partial response, or stable disease) was 80.0% (95% CI, 61.4-92.3%). Among the 15 patients with stable disease, 11 patients experienced >10% tumor shrinkage. Median progression-free survival was 5.8 months (95% CI, 4.1-7.6). Median overall survival was not reached at a median follow-up of 10.1 months. Grade 2 skin toxicity was observed in 23 patients, while no grade 3 skin toxicity was observed. Combined irinotecan and cetuximab is effective for pretreated metastatic wild-type KRAS colorectal cancer.
机译:这项研究的目的是前瞻性评估伊立替康和西妥昔单抗联合化疗在具有野生型KRAS的转移性结直肠癌预处理患者中的疗效。纳入接受伊立替康,奥沙利铂和氟嘧啶化疗后进展的转移性结直肠癌患者。使用Cycleave PCR方法评估KRAS状态;仅纳入无KRAS突变的患者。西妥昔单抗最初以400 mg / m(2)的剂量给药,然后每周进行250 mg / m(2)的输注。伊立替康每两周给药一次。从2008年10月到2009年4月,总共招募了30名患者。客观缓解率为30.0%(95%置信区间[CI],14.7-49.4%),疾病控制率(完全缓解,部分缓解或疾病稳定)为80.0%(95%CI,61.4-92.3%) 。在15位病情稳定的患者中,有11位患者的肿瘤缩小率> 10%。中位无进展生存期为5.8个月(95%CI,4.1-7.6)。中位随访10.1个月未达到中位总生存期。在23例患者中观察到2级皮肤毒性,而未观察到3级皮肤毒性。伊立替康和西妥昔单抗联合治疗可有效治疗转移性野生型KRAS大肠癌。

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