Managing Drug Interactions with Enzalutamide in Patients with Prostate Cancer: A Podcast.

IF 3.8 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Alicia K Morgans, Brooke Looney, Jesse Mack, Judeth Bianco
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引用次数: 0

Abstract

Enzalutamide is an oral androgen receptor signaling inhibitor used in the treatment of prostate cancer. Elderly patients with prostate cancer commonly have age-related comorbidities that require concomitant, active treatment. As a moderate inducer of the cytochrome P450 (CYP) enzymes CYP2C9 and CYP2C19, and a strong inducer of CYP3A4, there is potential for drug-drug interactions (DDIs) when enzalutamide is coadministered with other drugs that are CYP3A4 substrates-resulting in loss of efficacy or increased risk of unintended drug-related adverse events. In this podcast, we describe enzalutamide including its dosing, pharmacokinetics, and potential for interaction with coadministered drugs using several hypothetical patient cases with real-world clinical implications. Discussion of each patient case will highlight management strategies and illustrate that nearly all enzalutamide drug-drug interactions can be effectively managed with appropriate knowledge of which drugs pose interaction risks, when dose adjustments are indicated, and when alternative drugs can be substituted. Supplementary file1 (MP4 192541 KB).

管理前列腺癌患者与恩杂鲁胺的药物相互作用:播客。
恩杂鲁胺是一种用于治疗前列腺癌的口服雄激素受体信号抑制剂。老年前列腺癌患者通常有与年龄相关的合并症,需要同时积极治疗。作为细胞色素P450 (CYP)酶CYP2C9和CYP2C19的中度诱导剂,以及CYP3A4的强诱导剂,当enzalutamide与其他CYP3A4底物的药物共给药时,存在潜在的药物-药物相互作用(ddi) -导致疗效丧失或增加意外药物相关不良事件的风险。在这期播客中,我们介绍了恩杂鲁胺,包括它的剂量、药代动力学和与共给药药物的潜在相互作用,并使用了几个具有现实世界临床意义的假设病例。对每个患者病例的讨论将突出管理策略,并说明几乎所有enzalutamide -药物相互作用都可以有效管理,只要适当了解哪些药物会产生相互作用风险,何时需要调整剂量,以及何时可以替代药物。补充文件1 (MP4 192541 KB)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Safety
Drug Safety 医学-毒理学
CiteScore
7.60
自引率
7.10%
发文量
112
审稿时长
6-12 weeks
期刊介绍: Drug Safety is the official journal of the International Society of Pharmacovigilance. The journal includes: Overviews of contentious or emerging issues. Comprehensive narrative reviews that provide an authoritative source of information on epidemiology, clinical features, prevention and management of adverse effects of individual drugs and drug classes. In-depth benefit-risk assessment of adverse effect and efficacy data for a drug in a defined therapeutic area. Systematic reviews (with or without meta-analyses) that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. Original research articles reporting the results of well-designed studies in disciplines such as pharmacoepidemiology, pharmacovigilance, pharmacology and toxicology, and pharmacogenomics. Editorials and commentaries on topical issues. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Drug Safety Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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