首页> 外文OA文献 >Three-arm, randomized, phase 2 study of carboplatin and paclitaxel in combination with cetuximab, cixutumumab, or both for advanced non-small cell lung cancer (NSCLC) patients who will not receive bevacizumab-based therapy: An Eastern Cooperative Oncology Group (ECOG) study (E4508)
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Three-arm, randomized, phase 2 study of carboplatin and paclitaxel in combination with cetuximab, cixutumumab, or both for advanced non-small cell lung cancer (NSCLC) patients who will not receive bevacizumab-based therapy: An Eastern Cooperative Oncology Group (ECOG) study (E4508)

机译:三臂,卡铂和紫杉醇联合西妥昔单抗,西妥昔单抗或两者联合用于不接受贝伐单抗治疗的晚期非小细胞肺癌(NSCLC)患者的三阶段随机2期研究:东部合作肿瘤小组(ECOG )研究(E4508)

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摘要

BACKGROUND: Preclinical evidence supports the clinical investigation of inhibitors to the insulin-like growth factor receptor (IGFR) and the epidermal growth factor receptor (EGFR) either alone or in combination as treatment for patients with non-small cell lung cancer (NSCLC).METHODS: Patients with chemotherapy-naïve, advanced NSCLC who had an Eastern Cooperative Oncology Group performance status of 0 or 1 were eligible. Patients were randomized to receive carboplatin intravenously at an area under the plasma drug concentration-time curve of 6.0 plus paclitaxel 200 mg/m(2) intravenously on day 1 every 3 weeks combined with either intravenous cetuximab weekly (arm A), intravenous cixutumumab every 2 weeks (arm B), or both (arm C). Patients who had nonprogessing disease after 12 weeks of therapy were permitted to continue on maintenance antibody therapy until they developed progressive disease. The primary endpoint was progression-free survival (PFS). The study design required 180 eligible patients and had 88% power to detect a 60% increase in median PFS for either comparison (arm A vs arm C or arm B vs arm C) using the log-rank test.RESULTS: From September 2009 to December 2010, 140 patients were accrued. The study was closed to accrual early because of an excessive number of grade 5 events reported on arms A and C. Thirteen patients died during treatment (6 patients on arm A, 2 patients on arm B, and 5 patients on arm C), including 9 within approximately 1 month of starting therapy. The estimated median PFS for arms A, B, and C were similar at 3.4 months, 4.2 months, and 4 months, respectively.CONCLUSIONS: On the basis of the apparent lack of efficacy and excessive premature deaths, the current results do not support the continued investigation of carboplatin, paclitaxel, and cixutumumab either alone or in combination with cetuximab for patients with advanced NSCLC.
机译:背景:临床前证据支持单独或组合使用胰岛素样生长因子受体(IGFR)和表皮生长因子受体(EGFR)抑制剂治疗非小细胞肺癌(NSCLC)患者的临床研究。方法:东部合作肿瘤小组表现为0或1的未接受过化疗的晚期NSCLC患者是合格的。患者被随机分配在血浆药物浓度-时间曲线下的区域静脉注射卡铂,加紫杉醇200 mg / m(2),每3周静脉注射,每3周静脉联合西妥昔单抗静脉注射(A组),每次西妥昔单抗静脉注射2周(B组),或两周(C组)。治疗12周后患有非进展性疾病的患者被允许继续维持抗体治疗,直到他们发展为进行性疾病。主要终点是无进展生存期(PFS)。该研究设计需要180名合格患者,并且具有使用对数秩检验进行比较(A组vs C组或B组vs C组)的中位PFS升高60%的88%功效。结果:从2009年9月2010年12月,共有140例患者。由于在A臂和C臂上报告了过多的5级事件,该研究无法提前开始。治疗期间有13例患者死亡(A臂6例,B臂2例和C臂5例),包括9在开始治疗后约1个月内。结论A,B和C组的PFS中位数分别在3.4个月,4.2个月和4个月时相似。结论:由于明显缺乏疗效和过早死亡,目前的结果不支持继续对卡铂,紫杉醇和西妥昔单抗单独或与西妥昔单抗联用治疗晚期NSCLC患者进行了研究。

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