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Phase II trial of trimelamol in refractory ovarian cancer.

作者信息

Judson I R, Calvert A H, Gore M E, Balmanno K, Gumbrell L A, Perren T, Wiltshaw E

机构信息

Section of Drug Development, Institute of Cancer Research, Royal Marsden Hospital, UK.

出版信息

Br J Cancer. 1991 Feb;63(2):311-3. doi: 10.1038/bjc.1991.72.

Abstract

Trimelamol is an analogue of hexamethymelamine which exhibited activity against refractory ovarian cancer in phase I clinical trial. The dose limiting toxicity was leukopenia. In a phase II study, 42 patients with recurrent, or platinum-complex resistant, advanced ovarian cancer were treated using the dose schedule 800 mg m-2 i.v. daily for 3 days. There were one complete, three partial and five minor responses, objective response rate: 9.5%. The main toxicity observed was nausea and vomiting, myelosuppression was minor. The role of Trimelamol in the treatment of ovarian cancer remains to be defined, but its activity is limited in refractory disease.

摘要

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本文引用的文献

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In vitro cytotoxicity of the methylmelamines.甲基三聚氰胺的体外细胞毒性。
Chem Biol Interact. 1980 Feb;29(2):235-46. doi: 10.1016/0009-2797(80)90036-8.
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In vitro studies with hexamethylmelamine.六甲基三聚氰胺的体外研究。
Biochem Pharmacol. 1977 Dec 15;26(24):2385-91. doi: 10.1016/0006-2952(77)90446-4.

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