Department of Oncology, National Taiwan University Hospital, Taipei, Taiwan.
J Formos Med Assoc. 2010 May;109(5):338-44. doi: 10.1016/S0929-6646(10)60061-7.
BACKGROUND/PURPOSE: The efficacy and safety of chemotherapy as third- or higher-line therapy for advanced non-small cell lung cancer (NSCLC) are unclear. The purpose of this study was to evaluate the efficacy and safety of pemetrexed for heavily pretreated, advanced NSCLC.
We retrospectively reviewed advanced NSCLC patients who received pemetrexed and more than two prior chemotherapy regimens. The tumor responses were evaluated by the Response Evaluation Criteria of Solid Tumors. Progression-free survival and overall survival were calculated by the Kaplan-Meier method. Toxicity was evaluated according to the Common Terminology Criteria for Adverse Events version 3.0.
A total of 95 patients (53 men and 42 women) were included. The median age was 63 years (range, 29-83). Seventy (73.7%) patients had adenocarcinoma. The median number of prior systemic therapies was three (range, 2-7). The median number of cycles of pemetrexed therapy was four (range, 1-11). Seven (7.4%) patients achieved a partial response, and 33 (34.7%) had stable disease. The median progression-free survival was 11 6 days, and the median overall survival was 382 days. A trend toward increased progression-free survival was observed for patients who had non-squamous compared with squamous NSCLC.
Pemetrexed has modest efficacy for heavily pretreated NSCLC patients.
背景/目的:化疗作为晚期非小细胞肺癌(NSCLC)的三线或更高线治疗的疗效和安全性尚不清楚。本研究旨在评估培美曲塞治疗多线预处理的晚期 NSCLC 的疗效和安全性。
我们回顾性分析了接受培美曲塞和两线以上化疗方案的晚期 NSCLC 患者。采用实体瘤反应评价标准评估肿瘤反应。采用 Kaplan-Meier 法计算无进展生存期和总生存期。根据不良事件通用术语标准 3.0 评估毒性。
共纳入 95 例患者(53 例男性,42 例女性)。中位年龄为 63 岁(范围 29-83)。70 例(73.7%)患者为腺癌。中位既往系统治疗线数为 3 线(范围 2-7)。培美曲塞治疗的中位周期数为 4 个(范围 1-11)。7 例(7.4%)患者部分缓解,33 例(34.7%)疾病稳定。中位无进展生存期为 116 天,中位总生存期为 382 天。与鳞状 NSCLC 相比,非鳞状 NSCLC 患者的无进展生存期有增加的趋势。
培美曲塞对多线预处理的 NSCLC 患者具有适度疗效。