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晚期 NSCLC 的二线治疗。

Second-Line Therapy for Advanced NSCLC.

机构信息

Lineberger Comprehensive Cancer Center at the University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7305, USA.

出版信息

Oncologist. 2013;18(8):947-53. doi: 10.1634/theoncologist.2013-0096. Epub 2013 Aug 5.

Abstract

Most patients with lung cancer have non-small cell lung cancer (NSCLC) subtype and have advanced disease at the time of diagnosis. Improvements in both first-line and subsequent therapies are allowing longer survival and enhanced quality of life for these patients. The median overall survival observed in many second-line trials is approximately 9 months, and many patients receive further therapy after second-line therapy. The cytotoxic agents pemetrexed and docetaxel and the epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) erlotinib and gefitinib are standard second-line therapies. For patients with EGFR mutation, a TKI is the favored second-line therapy if not already used in first-line therapy. For patients without the EGFR mutation, TKIs are an option, but many oncologists favor cytotoxic therapy. The inhibitor of the EML4/ALK fusion protein, crizotinib, has recently become a standard second-line treatment for patients with the gene rearrangement and has promise for patients with the ROS1 rearrangement.

摘要

大多数肺癌患者为非小细胞肺癌(NSCLC)亚型,且在诊断时已处于疾病晚期。一线和二线治疗的改进使这些患者的生存时间延长,生活质量提高。许多二线试验观察到的中位总生存期约为 9 个月,许多患者在二线治疗后还会接受进一步的治疗。细胞毒性药物培美曲塞和多西他赛以及表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKI)厄洛替尼和吉非替尼是标准的二线治疗药物。对于 EGFR 突变患者,如果一线治疗中未使用 TKI,则 TKI 是首选的二线治疗药物。对于无 EGFR 突变的患者,TKI 是一种选择,但许多肿瘤学家更倾向于细胞毒性治疗。EML4/ALK 融合蛋白抑制剂克唑替尼最近已成为该基因重排患者的标准二线治疗药物,并且对 ROS1 重排患者也有疗效。

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Second-Line Therapy for Advanced NSCLC.晚期 NSCLC 的二线治疗。
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