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卡铂用于晚期恶性黑色素瘤的II期试验。

Phase II trial of carboplatin in advanced malignant melanoma.

作者信息

Evans L M, Casper E S, Rosenbluth R

出版信息

Cancer Treat Rep. 1987 Feb;71(2):171-2.

PMID:3542209
Abstract

Twenty-six evaluable patients with metastatic malignant melanoma who had not received prior chemotherapy were treated in a phase II study with carboplatin (CBDCA), 400 mg/m2 iv every 4 weeks. There were five partial responses of 3, 3+, 5, 7+, and 12+ months' duration. Thrombocytopenia was the dose-limiting toxicity; ten patients had transient platelet count depressions to less than 75,000/mm3. Mild to moderate nausea and/or vomiting occurred in 15 patients. Renal, auditory, and neurologic toxic effects were not encountered. Since the response rate of 19% (95% confidence limits, 8%-38%) is similar to that noted for dacarbazine, carboplatin, singly and in combination with other agents, needs further evaluation in patients with malignant melanoma.

摘要

在一项II期研究中,对26例未接受过先前化疗的转移性恶性黑色素瘤可评估患者采用卡铂(CBDCA)治疗,剂量为400mg/m²,静脉注射,每4周一次。有5例部分缓解,持续时间分别为3、3 +、5、7 +和12 +个月。血小板减少是剂量限制性毒性;10例患者血小板计数短暂降至低于75,000/mm³。15例患者出现轻至中度恶心和/或呕吐。未发现肾脏、听觉和神经毒性作用。由于19%的缓解率(95%置信区间,8%-38%)与达卡巴嗪单独或与其他药物联合使用时的缓解率相似,卡铂在恶性黑色素瘤患者中需要进一步评估。

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