Albayrak Aslınur, Düzenli Tuğdenur, Kayıkçıoğlu Erkan
Department of Clinical Pharmacy, Faculty of Pharmacy, Suleyman Demirel University, Isparta, Turkey.
Faculty of Pharmacy, Suleyman Demirel University, Isparta, Turkey.
J Cancer Res Clin Oncol. 2023 Sep;149(12):9621-9627. doi: 10.1007/s00432-023-04890-0. Epub 2023 May 24.
The aim of this study was to determine the drug profile of patients with non-small cell lung cancer (NSCLC) and to identify potential drug-drug interactions (PDDIs) during hospitalization. In particular, PDDIs in categories X and D were determined.
This retrospective cross-sectional study was conducted in the oncology services of a university hospital between 2018 and 2021. PDDIs were evaluated using Lexicomp Drug Interactions software included in UpToDate.
A total of 199 patients were included in the study. Polypharmacy was present in 92.5% of the patients and the median (min-max) number of drugs used was 8 (2-16). 32% of the patients had D and X PDDIs. A total of 16 PDDIs at risk grade X were found in 15 (7.5%) patients. A total of 81 PDDIs of risk grade D were found in 54 (27.1%) patients and a total of 276 PDDIs of risk grade C were identified in 97 (48.7%) patients. Anticancer drugs (p = 0.008), opioids (p = 0.046), steroids (p = 0.003), 5-HT3 receptor antagonists (p = 0.012), aprepitant (p = 0.025) and antihistamines (p < 0.001) were statistically more frequent among patients with PDDIs than among those without.
The results of our study indicated that polypharmacy and PDDIs are common in hospitalized patients with NSCLC cancer. The monitoring of medications is critical for maximizing therapeutic effects and minimizing side effects related to PDDIs. As a part of multidisciplinary team, clinical pharmacists can contribute significantly to preventing, detecting and managing PDDIs.
本研究的目的是确定非小细胞肺癌(NSCLC)患者的用药情况,并识别住院期间潜在的药物相互作用(PDDIs)。特别确定了X类和D类中的PDDIs。
本回顾性横断面研究于2018年至2021年在一家大学医院的肿瘤科室进行。使用UpToDate中包含的Lexicomp药物相互作用软件评估PDDIs。
本研究共纳入199例患者。92.5%的患者存在多药联用情况,使用药物的中位数(最小值-最大值)为8(2-16)种。32%的患者存在D类和X类PDDIs。在15例(7.5%)患者中发现了共16种风险等级为X的PDDIs。在54例(27.1%)患者中发现了共81种风险等级为D的PDDIs,在97例(48.7%)患者中识别出了共276种风险等级为C的PDDIs。与无PDDIs的患者相比,PDDIs患者中抗癌药物(p = 0.008)、阿片类药物(p = 0.046)、类固醇(p = 0.003)、5-羟色胺3受体拮抗剂(p = 0.012)、阿瑞匹坦(p = 0.025)和抗组胺药(p < 0.001)在统计学上更为常见。
我们的研究结果表明,多药联用和PDDIs在住院NSCLC患者中很常见。药物监测对于最大化治疗效果和最小化与PDDIs相关的副作用至关重要。作为多学科团队的一部分,临床药师可以在预防、检测和管理PDDIs方面做出重大贡献。