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DMXAA(ASA404)联合多西他赛用于晚期前列腺癌的潜力。

The potential of DMXAA (ASA404) in combination with docetaxel in advanced prostate cancer.

作者信息

McKeage Mark J

机构信息

The University of Auckland, School of Medical Sciences, Department of Pharmacology and Clinical Pharmacology, Private Bag 92019, Auckland, New Zealand.

出版信息

Expert Opin Investig Drugs. 2008 Jan;17(1):23-9. doi: 10.1517/13543784.17.1.23.

Abstract

5,6-Dimethylxanthenone-4-acetic acid (DMXAA) is a vascular disrupting agent that has demonstrated efficacy in combination with taxane-based chemotherapy in patients with advanced cancer. Complementary modes of action, a lack of pharmacokinetic interaction and distinct adverse effect profiles provide a strong rationale for combining these anticancer agents. In a Phase II trial in men with hormone refractory prostate cancer, DMXAA (ASA404) in combination with docetaxel achieved a prostate-specific antigen response in more patients than docetaxel therapy alone, and was generally well tolerated. Further clinical evaluation of this combination in this patient population is warranted.

摘要

5,6-二甲基呫吨酮-4-乙酸(DMXAA)是一种血管破坏剂,已证明其与基于紫杉烷的化疗联合应用于晚期癌症患者时具有疗效。互补的作用模式、缺乏药代动力学相互作用以及不同的不良反应谱为联合使用这些抗癌药物提供了有力的理论依据。在一项针对激素难治性前列腺癌男性患者的II期试验中,DMXAA(ASA404)与多西他赛联合使用比单独使用多西他赛治疗使更多患者出现前列腺特异性抗原反应,并且总体耐受性良好。有必要对该患者群体中这种联合用药进行进一步的临床评估。

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