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米托蒽醌:在晚期前列腺癌的II期试验中有适度活性。

Mitoxantrone: modest activity in a phase II trial in advanced prostate cancer.

作者信息

Osborne C K, Drelichman A, Von Hoff D D, Crawford E D

出版信息

Cancer Treat Rep. 1983 Dec;67(12):1133-5.

PMID:6652630
Abstract

Thirty-seven patients with metastatic prostate cancer refractory to endocrine therapy were treated in a phase II trial of mitoxantrone. Starting doses were 12 and 10 mg/m2 iv every 21 days for good-risk and poor-risk patients, respectively. Of the 35 evaluable patients, two had objective partial regression and five had stable disease. Response duration ranged from 7 to 17+ months. The drug was very well tolerated by these elderly patients; myelosuppression was the major toxic effect. We conclude that mitoxantrone has modest activity and acceptable toxicity in patients with advanced prostate cancer.

摘要

37例对内分泌治疗耐药的转移性前列腺癌患者接受了米托蒽醌的II期试验治疗。对于低危和高危患者,起始剂量分别为每21天静脉注射12和10mg/m²。在35例可评估患者中,2例出现客观部分缓解,5例病情稳定。缓解持续时间为7至17个多月。这些老年患者对该药物耐受性良好;骨髓抑制是主要的毒性作用。我们得出结论,米托蒽醌在晚期前列腺癌患者中具有适度的活性和可接受的毒性。

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