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针对非小细胞肺癌的 EGFR 单克隆抗体。

Monoclonal antibodies against EGFR in non-small cell lung cancer.

机构信息

Department of Medicine I, Medical University of Vienna, Austria.

出版信息

Crit Rev Oncol Hematol. 2011 Oct;80(1):1-9. doi: 10.1016/j.critrevonc.2010.10.008. Epub 2010 Nov 24.

Abstract

Blockade of the epidermal growth factor receptor (EGFR) by monoclonal antibodies is a strategy to improve outcome in patients with non-small cell lung cancer. Cetuximab, a chimeric anti-EGFR monoclonal antibody, has been studied in combination with different chemotherapy protocols in both phase II and phase III trials in patients with advanced NSCLC. In the phase III FLEX trial, cetuximab added to cisplatin/vinorelbine resulted in an absolute overall survival benefit of 1.2 months compared to the same chemotherapy alone in patients with advanced EGFR-expressing NSCLC. In the second phase III trial, cetuximab added to carboplatin plus paclitaxed failed to improve progression-free survival but suggested a survival benefit similar to that seen in the FLEX trial. However, the benefit in survival reached statistical significance only in the FLEX trial. A meta-analysis that included patients from four randomized trials confirmed the efficacy of cetuximab when added to chemotherapy. Thus addition of cetuximab to platinum-based chemotherapy represents a new treatment option for patients with advanced NSCLC. Matuzumab and panitumumab have also been evaluated in phase II trials. Necitumumab is currently evaluated in combination with chemotherapy in two randomized phase III trials.

摘要

表皮生长因子受体 (EGFR) 的单克隆抗体阻断是改善非小细胞肺癌患者预后的一种策略。西妥昔单抗,一种嵌合抗 EGFR 单克隆抗体,已在 II 期和 III 期临床试验中与不同的化疗方案联合用于晚期 NSCLC 患者。在 III 期 FLEX 试验中,与单独使用相同的化疗相比,西妥昔单抗联合顺铂/长春瑞滨可使晚期 EGFR 表达 NSCLC 患者的总生存期绝对获益 1.2 个月。在第二项 III 期试验中,西妥昔单抗联合卡铂加紫杉醇未能改善无进展生存期,但提示与 FLEX 试验中观察到的生存获益相似。然而,只有在 FLEX 试验中,生存获益才达到统计学意义。一项纳入四项随机试验的患者的荟萃分析证实了西妥昔单抗联合化疗的疗效。因此,西妥昔单抗联合铂类化疗代表了晚期 NSCLC 患者的一种新的治疗选择。马妥珠单抗和帕尼单抗也已在 II 期试验中进行了评估。尼妥珠单抗目前正在两项随机 III 期试验中联合化疗进行评估。

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