Department of Pharmacy, Fred Hutchinson Cancer Center, Seattle, WA, USA.
School of Pharmacy, University of Waterloo, Kitchener, Canada.
J Oncol Pharm Pract. 2024 Sep;30(6):1057-1072. doi: 10.1177/10781552241238198. Epub 2024 May 8.
The objective of this review is to provide an overview of common drug-drug interactions (DDIs) associated with prostate cancer treatments and outline recommendations for managing polypharmacy.
A literature search of PubMed, Embase, and CINAHL was carried out to identify pharmacokinetic and pharmacodynamic changes caused by DDIs that are relevant for prostate cancer patients, DDIs between prostate cancer therapies and co-administered medications (both prescription and over-the-counter), and measures to prevent DDIs. Medication package inserts were used to identify the impact of DDI on the prostate cancer therapy and suggested interventions.
No DDIs are expected for the LHRH agonists leuprolide acetate, histrelin, goserelin, or leuprolide mesylate. However, DDIs have been reported for GnRH antagonists, anti-androgens, PARP inhibitors, and taxanes. Although there are no confirmed DDIs for sipuleucel-T to date, it is not generally recommended to use sipuleucel-T concurrently with immunosuppressive medications. Interventions to prevent DDIs include the use of software that can detect clinically significant DDIs, up-to-date medication reconciliation, the inclusion of dedicated clinical pharmacists in cancer treatment teams, and patient/caregiver education.
Prostate cancer patients have a high risk of potential DDIs due to numerous new anti-cancer therapies, the increased use of treatment combinations, and the likelihood of comorbid conditions also requiring drug therapy. Drug-drug interaction screening software, up-to-date medication reconciliation, inclusion of oncology pharmacists on healthcare teams, and patient/caregiver education will aid the development of treatment plans that focus on achieving an optimal risk-benefit profile whilst reducing the risk of DDIs.
本文旨在概述与前列腺癌治疗相关的常见药物-药物相互作用(DDI),并提出管理多药治疗的建议。
通过对 PubMed、Embase 和 CINAHL 进行文献检索,确定了与前列腺癌患者相关的由 DDI 引起的药代动力学和药效学变化、前列腺癌治疗与合并用药(处方药和非处方药)之间的 DDI 以及预防 DDI 的措施。药物说明书用于确定 DDI 对前列腺癌治疗的影响,并提出干预建议。
LHRH 激动剂醋酸亮丙瑞林、曲普瑞林、戈舍瑞林或亮丙瑞林甲磺酸盐预计不会发生 DDI。然而,已报道 GnRH 拮抗剂、抗雄激素、PARP 抑制剂和紫杉烷类药物会发生 DDI。虽然迄今为止尚未确认 sipuleucel-T 有 DDI,但通常不建议同时使用 sipuleucel-T 和免疫抑制药物。预防 DDI 的干预措施包括使用能够检测出具有临床意义的 DDI 的软件、最新的药物一致性核对、在癌症治疗团队中纳入专门的临床药师,以及对患者/护理人员进行教育。
由于有许多新的抗癌疗法、治疗组合的使用增加以及合并症也需要药物治疗,因此前列腺癌患者有发生潜在 DDI 的高风险。药物-药物相互作用筛查软件、最新的药物一致性核对、在医疗保健团队中纳入肿瘤药师以及对患者/护理人员进行教育,将有助于制定注重实现最佳风险-获益平衡、同时降低 DDI 风险的治疗计划。