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表皮生长因子受体野生型晚期非小细胞肺癌的二线治疗:患者特征综述。

Second-line treatment in advanced non-small-cell lung cancer in the epidermal growth factor receptor wild-type population: review of patient profile.

机构信息

aMedical Oncology Service, Lucus Augusti University Hospital (HULA), Lugo bMedical Oncology Service, University Hospital of Vigo (CHUVI) cMedical Oncology Service, Povisa Hospital, Vigo dMedical Oncology Service, University Hospital Complex of Ourense (CHOU), Ourense eMedical Oncology Service, Arquitecto Marcide - Novoa Santos Hospital, Ferrol fMedical Oncology Service, Oncology Center of Galicia, A Coruña, Spain.

出版信息

Anticancer Drugs. 2014 Apr;25(4):368-74. doi: 10.1097/CAD.0000000000000066.

Abstract

After progression during first-line treatment in advanced non-small-cell lung cancer (NSCLC), a large percentage of patients are candidates for second-line treatment. The majority do not have epidermal growth factor receptor-activating mutations (EGFRwt). This article reviews the treatment options available for this subpopulation of patients, which includes essentially docetaxel, pemetrexed and erlotinib. These drugs all have similar efficacy, both in terms of objective response rates and overall survival, although with different toxicity profiles. In view of the similar efficacy of the three agents (docetaxel, pemetrexed and erlotinib) in the second-line treatment of NSCLC in the EGFRwt population, and although there are no prospective studies on predictive variables or new molecular markers available, selection of the treatment will depend on the histological type (pemetrexed); patient preference (oral as opposed to intravenous formulation); the presence of comorbid conditions; quality of life; previous or residual toxicities; the risk of neutropenia; response to and the duration of the first-line chemotherapy; and history of smoking.

摘要

在一线治疗期间进展后的晚期非小细胞肺癌(NSCLC)患者中,很大一部分是二线治疗的候选者。他们中的大多数患者没有表皮生长因子受体激活突变(EGFRwt)。本文综述了这部分患者的治疗选择,包括多西他赛、培美曲塞和厄洛替尼。这些药物在客观缓解率和总生存期方面都具有相似的疗效,尽管毒性谱不同。鉴于三种药物(多西他赛、培美曲塞和厄洛替尼)在 EGFRwt 人群中的二线治疗 NSCLC 中的疗效相似,而且目前尚无关于预测变量或新的分子标志物的前瞻性研究,因此治疗的选择将取决于组织学类型(培美曲塞);患者偏好(口服与静脉制剂);合并症的存在;生活质量;既往或残留毒性;中性粒细胞减少症的风险;一线化疗的反应和持续时间;以及吸烟史。

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