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CI-958用于激素难治性前列腺癌患者的II期研究。

Phase II study of CI-958 in patients with hormone refractory prostate carcinoma.

作者信息

Philip Kuebler J, Moore Timothy, Pritchard James, Kraut Eric

机构信息

Grant/Riverside Hospitals, Columbus, Ohio, USA.

出版信息

Invest New Drugs. 2004 Apr;22(2):181-4. doi: 10.1023/B:DRUG.0000011795.82694.80.

DOI:10.1023/B:DRUG.0000011795.82694.80
PMID:14739667
Abstract

A phase II trial of CI-958 (NSC #635371), a new benzothiopyranoindazole was performed in patients with hormone refractory prostate carcinoma using prostate specific antigen (PSA) levels for response assessment. Twenty-two patients were entered on this study and twenty one were eligible. Toxicity consisted mainly of granulocytopenia (71% grade 3 or 4), but there were no significant infections. Two patients were removed from study due to asymptomatic decreases in cardiac ejection fraction. Of 21 evaluable patients, there were four responders (19%, CI 0-35%).

摘要

一项针对新型苯并噻吩并吲哚CI-958(NSC #635371)的II期试验在激素难治性前列腺癌患者中进行,使用前列腺特异性抗原(PSA)水平进行疗效评估。22名患者进入该研究,21名符合条件。毒性主要包括粒细胞减少(71%为3级或4级),但无严重感染。两名患者因无症状的心脏射血分数下降而退出研究。在21名可评估患者中,有4名缓解者(19%,可信区间0-35%)。

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