Evaluation of oral targeted anticancer drug interactions and their management by oncology pharmacists

IF 1.3 Q4 PHARMACOLOGY & PHARMACY
Sarah L. Wede Pharm.D., Madeline D. Schultze, David J. Reeves Pharm.D.
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引用次数: 0

Abstract

Introduction

Oral targeted anticancer drugs (OTADs) have become a key component of therapy for multiple malignancies, and their use continues to expand. While several studies have identified numerous drug interactions (DIs) associated with these oral therapies, very few have described the role of an oncology pharmacist in DI management.

Objectives

The purpose of this study was to quantify moderate/severe DIs with OTADs at initiation and describe the role of the pharmacist in interaction detection and management.

Methods

This retrospective analysis was completed utilizing an electronic health record review of adult patients initiated on an OTAD with pharmacist documentation of medication review between July 2020 and July 2022. The outcomes of this study included the incidence of moderate/severe DIs, the distribution of pharmacokinetic/pharmacodynamic DIs, the incidence of pharmacist documentation of moderate/severe DIs, prescriber acceptance of documented pharmacist-recommended interventions, the evaluation of severe DIs, and presence of DI related adverse effects within 60 days of OTAD initiation.

Results

Two hundred sixty-six patients were included. Forty-six percent (122/266) of patients had at least one moderate/severe DI identified by investigators with a total of 220 moderate/severe DIs detected. Fifty-eight percent (127/220) of the identified DIs were pharmacokinetic and 42% (93/220) were pharmacodynamic in nature. Pharmacist documentation was present for 36% (75/207) of the moderate DIs and 92% (12/13) of the severe DIs identified at OTAD initiation, and prescribers accepted 94% (82/87) of the pharmacists' recommended interventions. Lastly, 12.5% (26/208) of the incidence of adverse effects was potentially related to moderate/severe DIs within 60 days of OTAD initiation.

Conclusion

Clinically significant (moderate/severe) DIs are common in patients receiving OTADs and may impact patient outcomes. Pharmacists can help to identify, prevent, and create a plan of action for the management of DIs and we advocate for their involvement in the management of OTAD therapies.

肿瘤药剂师对口服抗癌靶向药物相互作用及其管理的评估
引言 口服靶向抗癌药物(OTADs)已成为多种恶性肿瘤治疗的关键组成部分,其使用范围也在不断扩大。虽然已有多项研究发现了与这些口服疗法相关的多种药物相互作用(DIs),但很少有研究描述了肿瘤药剂师在 DI 管理中的作用。 本研究的目的是量化与 OTADs 开始时相关的中度/重度 DIs,并描述药剂师在相互作用检测和管理中的作用。 方法 通过对 2020 年 7 月至 2022 年 7 月期间使用 OTAD 的成人患者进行电子病历审查,并由药剂师提供用药审查记录,完成了这项回顾性分析。本研究的结果包括中度/重度药物相互作用的发生率、药动学/药效学药物相互作用的分布、药剂师记录中度/重度药物相互作用的发生率、处方者对药剂师建议的干预措施的接受程度、重度药物相互作用的评估以及开始使用 OTAD 后 60 天内出现的药物相互作用相关不良反应。 结果 共纳入 266 名患者。46%的患者(122/266)至少有一次中度/重度DI被研究人员发现,共发现220次中度/重度DI。在确定的 DI 中,58%(127/220)属于药代动力学性质,42%(93/220)属于药效学性质。在 OTAD 启动时发现的中度 DI 中,有 36% (75/207)和 92% (12/13)的严重 DI 有药剂师记录,处方者接受了 94% (82/87)药剂师建议的干预措施。最后,12.5%(26/208)的不良反应发生率可能与开始使用 OTAD 后 60 天内的中度/重度 DIs 有关。 结论 有临床意义的(中度/重度)DIs 在接受 OTADs 的患者中很常见,可能会影响患者的治疗效果。药剂师可以帮助识别、预防和制定处理 DIs 的行动计划,我们提倡药剂师参与 OTAD 治疗的管理。
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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CiteScore
2.70
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0.00%
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