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联合化疗在晚期非小细胞肺癌患者中具有适度的生存优势:一项加拿大多中心随机试验报告。

Combination chemotherapy confers modest survival advantage in patients with advanced non-small cell lung cancer: report of a Canadian multicenter randomized trial.

作者信息

Evans W K

机构信息

National Cancer Institute of Canada, Queen's University, Kingston, Ontario.

出版信息

Semin Oncol. 1988 Dec;15(6 Suppl 7):42-5.

PMID:2851177
Abstract

Between February 1983 and January 1986, the National Cancer Institute of Canada conducted a prospective randomized trial comparing best supportive care (BSC) with two chemotherapy regimens: Vindesine and cisplatin (Platinol) (VP) and cyclophosphamide, doxorubicin, and cisplatin (CAP). Twenty-three centers across Canada entered 251 patients on the basis of measurable or evaluable disease, with either distant metastases or bulky limited disease considered inoperable and unsuitable for radical radiation therapy; 233 patients were eligible for evaluation. The overall response rates on the chemotherapy arms were: VP, 25.3%; CAP, 15.3%. The median survival rates were: VP, 32.6 weeks; CAP, 24.7 weeks; BSC, 17 weeks. Toxicity on the chemotherapy arms was significant. Although better therapies are required, the data in this study clearly indicate that VP and CAP combination chemotherapy confers a modest survival advantage over BSC in advanced non-small cell lung cancer.

摘要

1983年2月至1986年1月期间,加拿大国家癌症研究所开展了一项前瞻性随机试验,将最佳支持治疗(BSC)与两种化疗方案进行比较:长春地辛和顺铂(VP)以及环磷酰胺、阿霉素和顺铂(CAP)。加拿大全国23个中心纳入了251例基于可测量或可评估疾病的患者,这些患者存在远处转移或大块局限性疾病,被认为无法手术且不适合根治性放射治疗;233例患者符合评估条件。化疗组的总体缓解率为:VP组25.3%;CAP组15.3%。中位生存率为:VP组32.6周;CAP组24.7周;BSC组17周。化疗组的毒性显著。尽管需要更好的治疗方法,但本研究中的数据清楚地表明,在晚期非小细胞肺癌中,VP和CAP联合化疗比最佳支持治疗具有适度的生存优势。

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