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晚期非小细胞肺癌患者的管理:现有和新兴选择。

Management of patients with advanced non-small cell lung cancer: current and emerging options.

机构信息

Yale Cancer Center/Yale University School of Medicine, New Haven, Connecticut, USA.

出版信息

Drugs. 2010;70(2):167-79. doi: 10.2165/11532200-000000000-00000.

Abstract

Systemic therapy for advanced non-small cell lung cancer (NSCLC) has evolved over the last two decades, with modest improvements in quality of life and overall survival. A plateau has been reached with traditional chemotherapy, and efforts are now being directed at developing molecularly targeted agents. To date, three such agents have been found to improve overall survival in advanced NSCLC. Erlotinib, a small-molecule inhibitor of the epidermal growth factor receptor, was approved by the US FDA in 2004 as second- or third-line treatment for advanced NSCLC. Bevacizumab, an antibody to vascular endothelial growth factor, a key mediator of angiogenesis, received approval in 2006, after a randomized trial reported a median survival of 1 year when bevacizumab was added to first-line chemotherapy. More recently, cetuximab, an antibody to the epidermal growth factor receptor, was found to improve outcome when added to chemotherapy, and FDA approval is anticipated. Several additional agents are currently being evaluated in randomized trials, with encouraging results from early studies. These and other studies are prospectively investigating predictive clinical and molecular characteristics, with the ultimate goal of individualizing therapy in advanced NSCLC.

摘要

在过去的二十年中,晚期非小细胞肺癌(NSCLC)的全身治疗已经发展,生活质量和总生存期都有了适度的提高。传统化疗已达到平台期,目前正在努力开发针对分子靶点的药物。迄今为止,已有三种此类药物被发现可改善晚期 NSCLC 的总生存期。表皮生长因子受体的小分子抑制剂厄洛替尼于 2004 年被美国 FDA 批准作为晚期 NSCLC 的二线或三线治疗药物。贝伐单抗是一种针对血管内皮生长因子的抗体,是血管生成的关键介质,在一项随机试验报告贝伐单抗联合一线化疗可使中位生存期延长至 1 年之后,于 2006 年获得批准。最近,西妥昔单抗是一种针对表皮生长因子受体的抗体,与化疗联合使用可改善预后,预计将获得 FDA 批准。目前正在对几种其他药物进行随机试验评估,早期研究结果令人鼓舞。这些和其他研究正在前瞻性地研究预测性的临床和分子特征,最终目标是使晚期 NSCLC 的治疗个体化。

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