Jung Sun Young, Yoo Su Jin, Shin Ji Young, Park Ji Won, Lee Jeong Eun, Park Hee Sun, Kim Ju Ock, Kim Sun Young
Department of Internal Medicine, Chungnam National University Hospital, Daejon, Korea.
Zhongguo Fei Ai Za Zhi. 2011 Jan;14(1):33-8. doi: 10.3779/j.issn.1009-3419.2011.01.07.
Pemetrexed have been approved for the treatment of patients affected by advanced non-small cell lung cancer (NSCLC) in progression after first-line chemotherapy. We evaluated the activity and feasibility of pemetrexed in previously treated NSCLC.
Patients with histologically or cytologically confirmed NSCLC were evaluated from April 2007 to March 2009. The patients had relapsed or progressed after prior chemotherapy treatment. Pemetrexed (500 mg/m²) was administered intravenously once every 3 weeks after progression to prior chemotherapy. The tumor response was evaluated according to RECIST criteria by chest CT at every 2 cycles of chemotherapy.
A total 61 patients were eligible for analysis. Performance status of them (100%) was over 2. The response rate and disease control rate were 14.7% and 37.7% respectively. Non-squamous cell carcinoma histology was significantly associated with a superior response rate (P=0.045) and disease control rate (P=0.008). The median survival time and the median progression free survival (PFS) time were 6.11 months and 2.17 months, respectively. Comparing the efficacy of pemetrexed in these two settings [second-line versus (12/61) more than third (49/61)], there was no significant difference in regard to median survival (11.18 months vs 11.46 months, P=0.922,5), but PFS was more longer in third- or further-line groups than second-line group (1.39 months vs 2.25 months, P=0.015,3).
Pemetrexed is a feasible regimen in previously treated NSCLC with poor performance status.
培美曲塞已被批准用于治疗一线化疗后病情进展的晚期非小细胞肺癌(NSCLC)患者。我们评估了培美曲塞在既往接受过治疗的NSCLC患者中的活性和可行性。
对2007年4月至2009年3月间组织学或细胞学确诊为NSCLC的患者进行评估。这些患者在先前化疗后复发或病情进展。在先前化疗进展后,每3周静脉注射一次培美曲塞(500mg/m²)。在每2个化疗周期时通过胸部CT根据RECIST标准评估肿瘤反应。
共有61例患者符合分析条件。他们的体能状态(100%)均超过2。有效率和疾病控制率分别为14.7%和37.7%。非鳞状细胞癌组织学与较高的有效率(P=0.045)和疾病控制率(P=0.008)显著相关。中位生存时间和中位无进展生存(PFS)时间分别为6.11个月和2.17个月。比较培美曲塞在这两种情况下的疗效[二线治疗组(12/61)与三线及以上治疗组(49/61)],中位生存期无显著差异(11.18个月对11.46个月,P=0.922,5),但三线及以上治疗组的PFS比二线治疗组长(1.39个月对2.25个月,P=0.015,3)。
培美曲塞是一种用于既往接受过治疗、体能状态较差的NSCLC患者的可行治疗方案。