New-generation androgen receptor signaling inhibitors (ARSIs) in metastatic hormone-sensitive prostate cancer (mHSPC): pharmacokinetics, drug-drug interactions (DDIs), and clinical impact.

Lorenzo Gasperoni, Emilio Francesco Giunta, Daniela Montanari, Carla Masini, Ugo De Giorgi
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Abstract

Introduction: The therapeutic scenario of metastatic hormone-sensitive prostate cancer (mHSPC) has dramatically changed in recent years, with the approval of new-generation Androgen Receptor Signaling Inhibitors (ARSIs), in combination with the androgen deprivation therapy (ADT), which was the previous standard of care. Despite showing a similar clinical efficacy, ARSIs, all of which are administered orally, are different in terms of pharmacokinetic and drug-drug interactions (DDIs).

Areas covered: This review covers the main pharmacokinetic characteristics of ARSIs that have been approved for the first-line therapy of mHSPC patients, underlying the differences among these molecules and focusing on the known or possible interactions with other drugs. Full-text articles and abstracts were searched in PubMed.

Expert opinion: Since prostate cancer occurs mainly in older age, comorbidities and the consequent polypharmacy increase the DDI risk in mHSPC patients who are candidates for ARSI. Waiting for new therapeutic options, in the absence of direct comparisons, pharmacokinetic knowledge is essential to guide clinicians in prescribing ARSI in this setting.

新一代雄激素受体信号抑制剂(ARSIs)在转移性激素敏感性前列腺癌(mHSPC)中的应用:药代动力学、药物间相互作用(DDIs)和临床影响。
导言:近年来,随着新一代雄激素受体信号抑制剂(ARSIs)与雄激素剥夺疗法(ADT)的联合应用,转移性激素敏感性前列腺癌(mHSPC)的治疗方案发生了巨大变化。尽管ARSIs显示出相似的临床疗效,但它们都是口服给药,在药代动力学和药物间相互作用(DDIs)方面存在差异:本综述涵盖了已获准用于mHSPC患者一线治疗的ARSIs的主要药代动力学特征,这些分子之间的差异是其根本原因,重点是已知或可能与其他药物发生的相互作用。在 PubMed 上检索了全文文章和摘要:专家意见:由于前列腺癌主要发生在老年人身上,合并症和随之而来的多重用药增加了作为 ARSI 候选药物的 mHSPC 患者的 DDI 风险。在等待新治疗方案的过程中,由于缺乏直接比较,药代动力学知识对于指导临床医生在这种情况下开具ARSI处方至关重要。
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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