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卡铂和长春瑞滨用于未经治疗的局部晚期和转移性非小细胞肺癌

Carboplatin and vinorelbine in untreated locally advanced and metastatic non-small cell lung cancer.

作者信息

Horvath L, Boyer M, Clarke S, Beale P, Beith J, Underhill C, Stockler M, Bishop J

机构信息

Sydney Cancer Centre, Sydney, NSW, Australia.

出版信息

Lung Cancer. 2001 May;32(2):173-8. doi: 10.1016/s0169-5002(00)00218-x.

Abstract

The aim of this study was to assess the activity and toxicity of carboplatin/vinorelbine combination chemotherapy in unresectable locally advanced and metastatic non-small cell lung cancer. Between April 1997 and June 1999 30 patients (22 M, eight F, median age 62) received treatment with carboplatin AUC 6 on day 1, and vinorelbine 25mg/m(2) on days 1, 8 and 15. Treatment was given every 28 days for six cycles unless progressive disease occurred. Twenty-three patients (77%) had stage IV disease, and seven (23%) stage IIIB. Ninety-three percent were WHO performance status 0-1. Twenty-three patients were fully assessable. Nine patients achieved partial responses (9/23, 39%) for an overall objective response rate of 9/30 (30%; 95% CI 15-49%). The median duration of response was 2.75 months (range 1-13 months). The median progression-free survival was 2 months and the median survival 5.25 months. The actuarial 1-year survival was 20%. The median number of cycles completed was two (range 1-6). Day 15 vinorelbine was administered in only 18% of cycles. The main toxicity was myelosuppression. WHO grade III/IV neutropenia was experienced in 50% of patients, however, there were only three episodes of febrile neutropenia. Eight patients required blood transfusion and one developed grade III thrombocytopenia. Treatment was ceased in one patient because of grade IV autonomic neuropathy. No patient had significant nausea and vomiting. There were no treatment-related deaths. These results indicate that carboplatin/vinorelbine is well tolerated and has similar activity to cisplatin/vinorelbine in patients with unresectable non-small cell lung cancer, however, the median survival was considerably shorter.

摘要

本研究旨在评估卡铂/长春瑞滨联合化疗在不可切除的局部晚期和转移性非小细胞肺癌中的活性及毒性。1997年4月至1999年6月期间,30例患者(男性22例,女性8例,中位年龄62岁)接受治疗,第1天给予卡铂AUC 6,第1、8和15天给予长春瑞滨25mg/m²。每28天进行一次治疗,共六个周期,除非出现疾病进展。23例患者(77%)为IV期疾病,7例(23%)为IIIB期。93%的患者世界卫生组织(WHO)体能状态为0 - 1级。23例患者可进行全面评估。9例患者获得部分缓解(9/23,39%),总体客观缓解率为9/30(30%;95%置信区间15 - 49%)。缓解持续时间的中位数为2.75个月(范围1 - 13个月)。无进展生存期的中位数为2个月,总生存期的中位数为5.25个月。1年生存率的精算值为20%。完成周期数的中位数为两个(范围1 - 6)。仅18%的周期在第15天给予长春瑞滨。主要毒性为骨髓抑制。50%的患者出现WHO III/IV级中性粒细胞减少,然而,仅发生3例发热性中性粒细胞减少。8例患者需要输血,1例出现III级血小板减少。1例患者因IV级自主神经病变而停止治疗。无患者出现明显恶心和呕吐。无治疗相关死亡。这些结果表明,卡铂/长春瑞滨耐受性良好,在不可切除的非小细胞肺癌患者中其活性与顺铂/长春瑞滨相似,然而,总生存期的中位数明显较短。

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