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伊立替康在非小细胞肺癌治疗中的当前作用。

Current role of irinotecan in the treatment of non-small-cell lung cancer.

作者信息

Kelly Karen

机构信息

Division of Medical Oncology, University of Colorado Health Sciences Center, Denver 80262, USA.

出版信息

Oncology (Williston Park). 2002 Sep;16(9):1153-62, 1165; discussion 1165-6 passim.

Abstract

Lung cancer remains the primary cause of cancer-related death in both men and women in the United States. Chemotherapy has been shown to provide a survival benefit in patients with advanced non-small-cell lung cancer (NSCLC), and current regimens have produced median survivals of approximately 8 months and 1-year survival rates of 30% to 35% in patients with stage IIIB and IVdisease. Nevertheless, there remains room for improvement. Irinotecan (CPT-II, Camptosar) has demonstrated efficacy in the treatment of small-cell lung cancer (SCLC). It also appears to have promising activity in advanced NSCLC, producing overall response rates of up to 32%. Combinations of irinotecan and cisplatin or carboplatin (Paraplatin) have resulted in overall response rates of 25% to 56% in phase II and III studies in patients with advanced disease, with median survivals ranging from 9 to 13 months and 1-year survival rates of 33% to 58%. Current irinotecan-based doublet and triplet regimens appear to produce promising response rates with manageable toxicities. In addition, irinotecan has demonstrated potential as a radiosensitizing agent and is currently being evaluated in several trials of combined-modality therapy in patients with locally advanced NSCLC. Early trials of irinotecan in combination with cisplatin or carboplatin along with radiation therapy have reported overall response rates of 60% to 67%. The approach appears to have potential and warrants further study.

摘要

在美国,肺癌仍是男性和女性癌症相关死亡的主要原因。化疗已被证明能使晚期非小细胞肺癌(NSCLC)患者的生存期受益,目前的治疗方案使ⅢB期和Ⅳ期患者的中位生存期约为8个月,1年生存率为30%至35%。然而,仍有改进的空间。伊立替康(CPT-II,开普拓)已在小细胞肺癌(SCLC)治疗中显示出疗效。它在晚期NSCLC中似乎也具有可观的活性,总缓解率高达32%。在晚期疾病患者的Ⅱ期和Ⅲ期研究中,伊立替康与顺铂或卡铂(铂尔定)联合使用的总缓解率为25%至56%,中位生存期为9至13个月,1年生存率为33%至58%。目前基于伊立替康的双联和三联方案似乎能产生可观的缓解率,且毒性可控。此外,伊立替康已显示出作为放射增敏剂的潜力,目前正在局部晚期NSCLC患者的几种联合治疗试验中进行评估。伊立替康与顺铂或卡铂联合放疗的早期试验报告总缓解率为60%至67%。这种方法似乎具有潜力,值得进一步研究。

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