Luong Thu-Lan T, Shou Karen J, Reinhardt Brian J, Kigelman Oskar F, Greenfield Kimberly M
Walter Reed National Military Medical Center, Bethesda, Maryland.
Tripler Army Medical Center, Honolulu, Hawaii.
Fed Pract. 2024 Aug;41(Suppl 3):S70-S82. doi: 10.12788/fp.0499. Epub 2024 Aug 15.
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.
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.
Of 702 patients prescribed paclitaxel, 338 completed treatment. Paclitaxel discontinuation alone vs concomitantly ( < .001) and 1 drug vs combination ( < .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.
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.
紫杉醇是一种用于治疗乳腺癌、肺癌、子宫内膜癌、宫颈癌、胰腺癌、肉瘤和胸腺瘤的抗肿瘤药物。然而,诱导、抑制细胞色素P450(CYP)同工酶2C8或3A4或作为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。本研究的目的是概述紫杉醇的使用情况,确定与紫杉醇相互作用的潜在药物,并描述其临床表现。
对接受紫杉醇治疗的患者进行回顾性分析,以评估癌症的类型和分期、治疗方案以及单独使用紫杉醇或紫杉醇与其他抗肿瘤药物联合使用的不良事件,使用的数据于2022年3月从美国国防部癌症登记处获取。此外,该研究比较了完成治疗的患者与中断治疗的患者的健康问题和处方。利用综合门诊/专业诊疗记录和药房数据交易服务数据库的数据,评估了紫杉醇与非癌症药物的相互作用,特别是代谢和抑制CYP3A4的抗抑郁药。数据于2022年10月获取。
在702例开具紫杉醇处方的患者中,338例完成了治疗。单独停用紫杉醇与同时停用(<0.001)以及使用一种药物与联合使用(<0.001)均具有统计学意义。同时服用较多处方药的紫杉醇患者的治疗中断率高于服用较少药物的患者。完成治疗组的患者接受了9至56种处方药,而中断治疗组的患者被开具了6至70种。中断治疗的患者比完成治疗的患者有更多已诊断的健康问题。
该研究全面概述了1996年至2022年期间紫杉醇的使用情况,并突出了可能影响治疗结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,但紫杉醇与抗抑郁药没有显著的药物相互作用。