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伊立替康、顺铂和依托泊苷用于敏感复发性小细胞肺癌的多机构II期试验。

Multi-institutional phase II trial of irinotecan, cisplatin, and etoposide for sensitive relapsed small-cell lung cancer.

作者信息

Goto K, Sekine I, Nishiwaki Y, Kakinuma R, Kubota K, Matsumoto T, Ohmatsu H, Niho S, Kodama T, Shinkai T, Tamura T, Ohe Y, Kunitoh H, Yamamoto N, Nokihara H, Yoshida K, Sugiura T, Matsui K, Saijo N

机构信息

Division of Thoracic Oncology, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577, Japan.

出版信息

Br J Cancer. 2004 Aug 16;91(4):659-65. doi: 10.1038/sj.bjc.6602056.

Abstract

Irinotecan (CPT-11) has been shown to exhibit excellent antitumour activity against small-cell lung cancer (SCLC). A multi-institutional phase II study was therefore conducted to evaluate the efficacy and toxicity of CPT-11 combined with cisplatin (CDDP) and etoposide (ETOP) (PEI regimen) for the treatment of sensitive relapsed SCLC. Patients who responded to first-line chemotherapy but relapsed more than 8 weeks after the completion of first-line therapy (n=40) were treated using the PEI regimen, which consisted of CDDP (25 mg m(-2)) weekly for 9 weeks, ETOP (60 mg m(-2)) for 3 days on weeks 1, 3, 5, 7, and 9, and CPT-11 (90 mg m(-2)) on weeks 2, 4, 6, and 8 with granulocyte colony-stimulating factor support. Five complete responses and 26 partial responses were observed, and the overall response rate was 78% (95% confidence interval 61.5-89.2%). The median survival time was 11.8 months, and the estimated 1-year survival rate was 49%. Grade 3/4 leucocytopenia, neutropenia, and thrombocytopenia were observed in 55, 73, and 33% of the patients, respectively. Nonhaematological toxicities were mild and transient in all patients. In conclusion, the PEI regimen is considered to be highly active and well tolerated for the treatment of sensitive relapsed SCLC.

摘要

伊立替康(CPT - 11)已显示出对小细胞肺癌(SCLC)具有出色的抗肿瘤活性。因此,开展了一项多机构的II期研究,以评估CPT - 11联合顺铂(CDDP)和依托泊苷(ETOP)(PEI方案)治疗敏感复发SCLC的疗效和毒性。对一线化疗有反应但在一线治疗完成后8周以上复发的患者(n = 40)采用PEI方案治疗,该方案包括每周一次给予CDDP(25 mg m(-2)),共9周;在第1、3、5、7和9周的3天内给予ETOP(60 mg m(-2));在第2、4、6和8周给予CPT - 11(90 mg m(-2)),并给予粒细胞集落刺激因子支持。观察到5例完全缓解和26例部分缓解,总缓解率为78%(95%置信区间61.5 - 89.2%)。中位生存时间为11.8个月,估计1年生存率为49%。分别有55%、73%和33%的患者出现3/4级白细胞减少、中性粒细胞减少和血小板减少。所有患者的非血液学毒性均较轻且为短暂性。总之,PEI方案被认为对治疗敏感复发SCLC具有高活性且耐受性良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54c8/2364791/3dc9a16f4530/91-6602056f1.jpg

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