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VP-16 and carboplatin in previously untreated patients with extensive small cell lung cancer: a study of the National Cancer Institute of Canada Clinical Trials Group.

机译:先前未接受治疗的大面积小细胞肺癌患者中的VP-16和卡铂:加拿大国家癌症研究所临床试验小组的一项研究。

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摘要

Thirty-four previously untreated patients with extensive small cell lung cancer were treated with a combination of carboplatin 300 mg m-2 i.v. on day 1 and etoposide 100 mg m-2 i.v. on days 1, 2 and 3 every 28 days. Thirty-two patients were assessable for response. Eighteen patients (56%) achieved an objective response (95% confidence limits 38%-73%). Five (16%) had a complete response and 13 (41.0%) had a partial response. The median time to response was 7.8 weeks and the median duration of response was 23.1 weeks (range 6.2 to 54 weeks). The median survival of all 34 extensive disease patients was 34.7 weeks (range 1.3-59.3 weeks). Myelosuppression (leukopenia) was the main toxicity. There was one early death that may have been treatment-related. Biochemical renal dysfunction was noted in two patients. Paresthesiae and tinnitus/hearing loss were described by three and two patients respectively. Serious gastrointestinal toxicity was infrequent. This and other studies have shown this combination to be active and well tolerated in small cell lung cancer; however, it is not yet clear if it is as efficacious as the more commonly used VP-16-cisplatin regimen.
机译:34例先前未接受治疗的广泛性小细胞肺癌患者接受卡铂300 mg m-2 i.v.的联合治疗。在第1天和依托泊苷100 mg m-2 i.v.每28天的第1、2和3天。可评估32例患者的反应。 18位患者(56%)达到了客观反应(95%置信范围38%-73%)。 5人(16%)有完全反应,13人(41.0%)有部分反应。中位反应时间为7.8周,中位反应时间为23.1周(范围为6.2至54周)。所有34名广泛疾病患者的中位生存时间为34.7周(范围1.3-59.3周)。骨髓抑制(白细胞减少)是主要的毒性反应。一例可能与治疗有关的早期死亡。两名患者发现生化肾功能不全。分别由三名和两名患者描述了感觉异常和耳鸣/听力丧失。很少有严重的胃肠道毒性。这项研究和其他研究表明,这种组合在小细胞肺癌中是有效的并且具有良好的耐受性。但是,尚不清楚它是否与更常用的VP-16-顺铂方案一样有效。

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