1 Department of Chemotherapy, Zhejiang Cancer Hospital, Hangzhou 310022, China ; 2 Key Laboratory Diagnosis and Treatment Technology on Thoracic Oncology, Hangzhou 310022, China.
J Thorac Dis. 2014 Jun;6(6):856-60. doi: 10.3978/j.issn.2072-1439.2014.06.15.
The aim of this study was to evaluate the feasibility and safety of retreatment the pemetrexed after the failure prior pemetrexed-based chemotherapy in non-small cell lung cancer (NSCLC) from our institute.
Patients with advanced NSCLC who were admitted to Zhejiang Cancer Hospital from Dec 2009 to Dec 2012 were retrospectively analyzed. All of the patients were given pemetrexed chemotherapy after the prior pemetrexed-based treatment. Survival analysis was evaluated by Kaplan-Meier method.
Twenty-five patients were included in current study. Initial pemetrexed-based therapy was given as first-line treatment in all patients. Nine patients retreated with pemetrexed as the fourth-line treatment, and sixteen as further-line. One patient (4%) achieved partial response (PR), 9 (36%) with stable disease (SD), and 15 (60%) had progressive disease (PD). The disease control rate (DCR) was 40% and the median progression-free survival (PFS) was 1.5 months (95% CI: 0.8-2.4 months). Patients with an initial PFS >6 months had a median PFS after retreatment of 2.2 months, while patients with an initial pemetrexed PFS ≤6 months had a median PFS after retreatment of 1.1 months (P=0.036). The toxicities associated with the 2nd pemetrexed were generally acceptable.
Retreatment of pemetrexed seems to be a potential therapeutic option for treatment of selected advanced NSCLC patients after failure of initial pemetrexed therapy, especially for the patients with a PFS more than 6 months in the initial pemetrexed treatment.
本研究旨在评估我院晚期非小细胞肺癌(NSCLC)患者在培美曲塞为基础的化疗失败后再次使用培美曲塞的可行性和安全性。
回顾性分析 2009 年 12 月至 2012 年 12 月期间在浙江省肿瘤医院接受治疗的晚期 NSCLC 患者。所有患者在先前培美曲塞治疗后均接受培美曲塞化疗。采用 Kaplan-Meier 法进行生存分析。
本研究共纳入 25 例患者。所有患者初始培美曲塞治疗均为一线治疗。9 例患者在培美曲塞治疗后进行四线治疗,16 例患者进行进一步治疗。1 例患者(4%)部分缓解(PR),9 例(36%)患者疾病稳定(SD),15 例(60%)患者疾病进展(PD)。疾病控制率(DCR)为 40%,中位无进展生存期(PFS)为 1.5 个月(95%CI:0.8-2.4 个月)。初始 PFS>6 个月的患者再次治疗后的中位 PFS 为 2.2 个月,而初始培美曲塞 PFS≤6 个月的患者再次治疗后的中位 PFS 为 1.1 个月(P=0.036)。第 2 次使用培美曲塞的毒性通常是可以接受的。
对于初始培美曲塞治疗失败的晚期 NSCLC 患者,培美曲塞再次治疗似乎是一种潜在的治疗选择,特别是对于初始培美曲塞治疗中 PFS 超过 6 个月的患者。