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S-1 和吉西他滨二线化疗治疗铂类耐药的非小细胞肺癌的长期疗效:一项 II 期研究。

Long-term administration of second-line chemotherapy with S-1 and gemcitabine for platinum-resistant non-small cell lung cancer: a phase II study.

机构信息

Department of Respirology (B2), Graduate School of Medicine, Chiba University, Chiba, Japan.

出版信息

J Thorac Oncol. 2011 Jan;6(1):156-60. doi: 10.1097/JTO.0b013e3181f7c76a.

Abstract

BACKGROUND

Standard second-line chemotherapies for non-small cell lung cancer (NSCLC) have been established but have limited clinical relevance. S-1 is a recently developed agent with potential activity against NSCLC.

METHODS

Patients with confirmed NSCLC recurrence after previous single- or two-regimen chemotherapy with platinum, performance status of 0 to 1, adequate organ functions, and measurable lesions were treated with S-1 (60 mg/m/d, twice a day) on days 1 to 14 and gemcitabine (1000 mg/m) on days 8 and 15, which were repeated every 3 weeks until tumor progression.

RESULTS

Treatment was administered for a median of 4 courses (range, 1-13) over a median of 125-day period in 34 patients. The overall response rate was 23.5% (no complete response and eight partial response; 95% confidence interval: 9.1-38.0%). The median progression-free and overall survival times were 6.6 and 19.9 months, respectively. The 1- and 2-year survival rates were 58.8 and 30.9%, respectively. Toxicity was mild during the entire treatment period, except for three grade 3 interstitial pneumonia.

CONCLUSION

The primary end point was met with the relatively high overall response rate. Randomized phase III studies for elucidating survival outcome of the regimen are warranted.

摘要

背景

非小细胞肺癌(NSCLC)的标准二线化疗方案已经确立,但临床相关性有限。S-1 是一种新开发的药物,对 NSCLC 具有潜在的活性。

方法

对先前接受过铂类单药或两药化疗且复发的 NSCLC 患者,根据体能状态(PS)评分 0-1、器官功能充足、有可测量病灶,给予 S-1(60mg/m/d,每天两次)治疗,第 1-14 天;吉西他滨(1000mg/m)治疗,第 8 和 15 天,每 3 周重复,直至肿瘤进展。

结果

34 例患者中位治疗 4 个疗程(范围,1-13),中位治疗时间为 125 天。总缓解率为 23.5%(无完全缓解,8 例部分缓解;95%置信区间:9.1-38.0%)。中位无进展生存期和总生存期分别为 6.6 和 19.9 个月。1 年和 2 年生存率分别为 58.8%和 30.9%。除 3 例 3 级间质性肺炎外,整个治疗期间毒性较轻。

结论

主要终点达到了较高的总缓解率。需要进行随机 III 期研究以阐明该方案的生存结果。

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