恩杂鲁胺及其主要代谢物在真实世界转移性去势抵抗性前列腺癌患者队列中的暴露反应评估

M. Nuland, A. Bergman, H. Rosing, N. Vries, A. Huitema, J. Beijnen
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引用次数: 9

摘要

恩杂鲁胺是一种口服药物,用于治疗转移性去势抵抗性前列腺癌(mCRPC);N -去甲基enzalutamide是其活性代谢物,具有与enzalutamide相似的临床相关抗雄激素能力,羧酸enzalutamide是一种非活性代谢物。本研究的目的是在真实世界的mCRPC患者队列中调查恩杂鲁胺和N -去甲基恩杂鲁胺暴露与治疗反应之间的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exposure‐Response Assessment of Enzalutamide and Its Major Metabolites in a Real‐World Cohort of Patients with Metastatic Castration‐Resistant Prostate Cancer
Enzalutamide is an oral agent for the treatment of metastatic castration‐resistant prostate cancer (mCRPC); N‐desmethyl enzalutamide is its active metabolite, which has clinically relevant anti‐androgen capacities similar to enzalutamide, and carboxylic acid enzalutamide is an inactive metabolite. The aim of our study was to investigate the relationship between enzalutamide and N‐desmethyl enzalutamide exposure and treatment response in a real‐world cohort of patients with mCRPC.
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