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米托蒽醌、二羟基蒽二酮和脱氧助间型霉素的临床试验现状。

Current status of clinical trials of m-AMSA, dihydroxyanthracenedione, and deoxycoformycin.

作者信息

Macdonald J S, Marsoni S, Bruno S, Poster D

出版信息

Recent Results Cancer Res. 1982;80:323-30. doi: 10.1007/978-3-642-81685-7_52.

Abstract

The current status of three drugs of clinical interest to the National Cancer Institute is reviewed. m-AMSA, a drug with a wide spectrum of activity in murine tumors, is now in phase II trial and has shown itself to have a high order of activity in acute nonlymphocytic leukemia. Dihydroxyanthracenedione, a compound with some of the characteristics of anthracyclines but with no cardiac toxicity in animal toxicology studies, is in phase I evaluation. Deoxycoformycin, an adenosine analog which is a potent inhibitor of adenosine deaminase, has shown moderate activity in acute leukemia patients in phase I trials, and has the potential to produce synergistic antitumor toxicity when used with arabinofuranosyladenine.

摘要

本文综述了美国国立癌症研究所感兴趣的三种临床药物的现状。m-AMSA是一种对鼠类肿瘤具有广泛活性的药物,目前正处于II期试验阶段,已证明其在急性非淋巴细胞白血病中具有较高的活性。二羟基蒽二酮是一种具有一些蒽环类药物特性但在动物毒理学研究中无心脏毒性的化合物,正在进行I期评估。脱氧助间型霉素是一种腺苷类似物,是腺苷脱氨酶的有效抑制剂,在I期试验中已显示对急性白血病患者有中度活性,并且与阿糖腺苷联合使用时有产生协同抗肿瘤毒性的潜力。

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