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伊立替康联合顺铂治疗晚期非小细胞肺癌患者。

Irinotecan plus cisplatin in patients with advanced non-small-cell lung cancer.

作者信息

Devore R, Johnson D, Crawford J, Dimery I, Eckardt J, Eckhardt S G

机构信息

Thoracic Oncology Program, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

出版信息

Oncology (Williston Park). 1998 Aug;12(8 Suppl 6):79-83.

PMID:9726097
Abstract

During the 1980s, platinum-based regimens were yielding response rates typically less than 25%, median survival durations of about 25 weeks, and 1-year survival rates less than 25% in patients with advanced non-small-cell lung cancer (NSCLC). Currently, results from single institution phase II trials of agents introduced in the 1990s show a doubling of these numbers, and results from multiinstitutional trials are demonstrating response rates ranging from 30% to 40%, median survival durations of 40 weeks, and 1 year survivals of 40%. Single agent irinotecan shows significant activity against NSCLC in preclinical and early phase I/II clinical studies, with activity similar to that for other new agents. Therapeutic synergy is observed in preclinical tumor models when irinotecan and cisplatin are combined, and phase I/II trials of this combination have demonstrated response rates > or = 50%. Herein the author provides an overview of data from phase II trials of irinotecan and focuses on preliminary results of a large US multicenter phase II trial of weekly irinotecan plus monthly cisplatin in 52 patients with advanced NSCLC. A response rate of 28.9% (95% CI, 16.5%-41.2%) and a median survival of 9.9 months were observed in this trial. US studies to design a more optimal irinotecan/cisplatin regimen in the same patient population are ongoing, and early results are encouraging.

摘要

在20世纪80年代,对于晚期非小细胞肺癌(NSCLC)患者,基于铂类的治疗方案的缓解率通常低于25%,中位生存期约为25周,1年生存率低于25%。目前,20世纪90年代引入药物的单机构II期试验结果显示这些数字翻了一番,多机构试验结果显示缓解率在30%至40%之间,中位生存期为40周,1年生存率为40%。在临床前和早期I/II期临床研究中,单药伊立替康对NSCLC显示出显著活性,其活性与其他新药相似。当伊立替康和顺铂联合使用时,在临床前肿瘤模型中观察到治疗协同作用,并且该联合方案的I/II期试验已证明缓解率≥50%。在此,作者概述了伊立替康II期试验的数据,并重点关注一项美国大型多中心II期试验的初步结果,该试验对52例晚期NSCLC患者采用每周一次伊立替康加每月一次顺铂的方案。在该试验中观察到缓解率为28.9%(95%CI,16.5%-41.2%),中位生存期为9.9个月。美国正在进行研究,以在同一患者群体中设计更优化的伊立替康/顺铂方案,早期结果令人鼓舞。

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