军队医疗系统中紫杉醇药物之间的相互作用。

Thu-Lan T Luong, Karen J Shou, Brian J Reinhardt, Oskar F Kigelman, Kimberly M Greenfield
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引用次数: 0

摘要

背景:紫杉醇是一种抗肿瘤药物,用于治疗乳腺癌、肺癌、子宫内膜癌、宫颈癌、胰腺癌、肉瘤和胸腺瘤。然而,诱导、抑制细胞色素 P450(CYP)同工酶 2C8 或 3A4 或其底物的药物可能会改变紫杉醇的代谢,从而可能影响其疗效。本研究旨在概述紫杉醇的使用情况,找出可能与紫杉醇发生相互作用的药物,并描述其临床表现:方法:利用2022年3月从美国国防部癌症登记处获取的数据,对接受紫杉醇治疗的患者进行回顾性分析,评估癌症类型和分期、治疗方案以及紫杉醇单药或紫杉醇联合其他抗肿瘤药物的不良反应。此外,该研究还比较了完成治疗和停止治疗的患者的健康问题和处方。研究利用综合门诊/专业就诊记录和药房数据交易服务数据库中的数据,评估了紫杉醇与非抗癌药物的相互作用,尤其是代谢和抑制CYP3A4的抗抑郁药。数据检索时间为 2022 年 10 月:在702名开具紫杉醇处方的患者中,有338人完成了治疗。紫杉醇单独停药与同时停药(P < .001)、单药停药与联合停药(P < .001)均有统计学意义。与接受较少药物治疗的患者相比,紫杉醇与更多处方药同时服用的患者中断治疗的比例更高。完成治疗组患者服用的处方药从9种到56种不等,而中止治疗组患者服用的处方药从6种到70种不等。与完成治疗的患者相比,中断治疗的患者有更多的医疗诊断问题:该研究全面概述了从 1996 年到 2022 年紫杉醇的使用情况,并强调了可能影响治疗效果的潜在药物相互作用。虽然处方药对紫杉醇停药的影响尚不确定,但紫杉醇和抗抑郁药并没有明显的药物相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Paclitaxel Drug-Drug Interactions in the Military Health System.

Background: Paclitaxel is an antineoplastic agent used to treat breast, lung, endometrial, cervical, pancreatic, sarcoma, and thymoma cancer. However, drugs that induce, inhibit, or are substrates of cytochrome P450 (CYP) isoenzymes 2C8 or 3A4 may alter the metabolism of paclitaxel, potentially impacting its effectiveness. The purposes of this study are to provide an overview of paclitaxel use, identify potential drugs that interact with paclitaxel, and describe their clinical manifestations.

Methods: A retrospective analysis was performed on patients receiving paclitaxel to evaluate types and stages of cancer, treatment regimens, and adverse events of paclitaxel alone or paclitaxel in combination with other antineoplastic drugs, using data retrieved in March 2022 from the US Department of Defense Cancer Registry. Additionally, the study compared the health issues and prescriptions of patients who completed treatment with those who discontinued treatment. It evaluated interactions of paclitaxel with noncancer drugs, particularly antidepressants metabolizing and inhibiting CYP3A4, using data from the Comprehensive Ambulatory/Professional Encounter Record and the Pharmacy Data Transaction Service database. Data were retrieved in October 2022.

Results: Of 702 patients prescribed paclitaxel, 338 completed treatment. Paclitaxel discontinuation alone vs concomitantly (P < .001) and 1 drug vs combination (P < .001) both were statistically significant. Patients who took paclitaxel concomitantly with a greater number of prescription drugs had a higher rate of treatment discontinuation than those who received fewer medications. Patients in the completed group received 9 to 56 prescription drugs, and those in the discontinued group were prescribed 6 to 70. Those who discontinued treatment had more diagnosed medical issues than those who completed treatment.

Conclusions: The study provides a comprehensive overview of paclitaxel usage from 1996 through 2022 and highlights potential drug interactions that may affect treatment outcomes. While the impact of prescription drugs on paclitaxel discontinuation is uncertain, paclitaxel and antidepressants do not have significant drug-drug interactions.

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