摘要
目的评估青西他滨联合顺铂治疗晚期非小细胞肺癌(NSCLC)的近期疗效和安全性。方法对35例晚期NSC∽患者采用吉西他滨1000me,/m2,静滴,第1、8天;顺铂25mg/m2,静滴,第1—3天。28d为1个周期,2个周期后进行一次疗效评价。结果35例患者中完全缓解(CR)0例,部分缓解(PR)14例,稳定(sD)16例,进展(PD)5例,总有效率(cR+PR)为40.0%。初治组有效率为52.2%,显著高于复治组的116.7%(P〈0.05)。中位疾病进展时间(个rP)6个月。主要毒副作用是骨髓抑制和胃肠道反应。结论GP方案对晚期NSCLC疗效较好,毒副反应轻,是晚期NSCLC特别是初治者的有效治疗方案。
Objective To investigate the efficacy and toxicities of gemcitabine and cisplatin as a chemother- apy regimen for patients with advancd non-small cell lung cancer (NSCLC). Methods Thirty-five patients with NSCLC were enrolled in this study. Gemclitabine was given on day 1 and 8 at a dose of 1000 mg/m2 and cisplatin at a dose of 25 mg,/m2 on day 1 to 3, The chemotherapy was repeated ever), 28 days, after 2 cycles for evaluating response. Results Complete response (CR) ,partial ~sponse (PR),stable disease (SD) and progressive disease (PD) were observed in 0,14,16 and 5 cases,respectiYely,with a response rate (RR) of 40. 0%. The RR in initial treatment group was found more than that inthe retreatment group ( 52, 2% vs 16.7%, P 〈 0. 05 ). The main toxicities were tol- erable,which inclvded myelosupp ession^nausea, vomiting, and liver damage. Conclusion Gemcitabine combined with cisplatin is effective and safe in the treatment of NSCLC ,especlally in the initial treatment patients.
出处
《中国基层医药》
CAS
2010年第4期445-446,共2页
Chinese Journal of Primary Medicine and Pharmacy
关键词
癌
非小细胞肺
吉西他滨
顺铂
Carcinoma non-small.veil lung cancer
Gemcitabine
Cisplatin