Department of Clinical Pharmacy, Faculty of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran.
Department of Internal Medicine, Haematology Section, Isfahan University of Medical Sciences, Isfahan, Iran.
J Oncol Pharm Pract. 2021 Jan;27(1):46-53. doi: 10.1177/1078155220910209. Epub 2020 Mar 17.
Patients suffering from solid tumors use a wide range of cytotoxic drugs. In this study, we aimed to detect, document, and descriptively analyze the potential drug-drug interactions in hospitalized solid tumor's patients in a Middle Eastern referral oncology-hematology University-affiliated hospital.
In this cross-sectional study, the medical record of solid tumor's patients who were admitted to the referral oncological center in Isfahan, Iran, during the six months period (2018) were considered. We included all patients who had received at least two chemotherapy or nonchemotherapy drugs simultaneously. The potential drug-drug interactions between chemotherapy and nonchemotherapy drugs were evaluated with Lexi-Interact ver.1.1 online software.
During the study period, a total of 141 cancer patients were recruited, and their drug therapy regiment was thoroughly analyzed. We detected 227 drug-drug interactions with moderate or major severity out of included patients in which 96, 71, 32, and 28 interactions were in the category of C, D, B, and X, respectively. One hundred and fourteen patients (80.8%) encountered at least one potential drug-drug interactions during their hospitalization. Mechanistically, most of drug-drug interactions (56.4%) were pharmacodynamics. Interaction between granisetron and metoclopramide were the top 10 detected interaction (11.4%). The interaction between docetaxel and carboplatin was the most frequent drug-drug interactions between oncology drugs (2.6% of total drug-drug interactions).
Potentially moderate or major drug-drug interactions frequently occur among solid tumor's cancer patients necessitate the establishment of a clinical pharmacy service for providing relevant pharmacotherapy consultations to prevent this potentially serious concern.
患有实体瘤的患者会使用多种细胞毒性药物。在这项研究中,我们旨在检测、记录和描述性分析在一家中东地区肿瘤学-血液学大学附属医院住院的实体瘤患者中的潜在药物-药物相互作用。
在这项横断面研究中,我们考虑了在伊朗伊斯法罕转诊肿瘤中心住院的实体瘤患者的病历,这些患者在六个月期间(2018 年)接受了至少两种化疗或非化疗药物的同时治疗。我们使用 Lexi-Interact ver.1.1 在线软件评估了化疗药物和非化疗药物之间的潜在药物-药物相互作用。
在研究期间,共招募了 141 名癌症患者,并对他们的药物治疗方案进行了彻底分析。我们在纳入的患者中发现了 227 种具有中度或重度严重程度的药物-药物相互作用,其中 96、71、32 和 28 种相互作用分别属于 C、D、B 和 X 类。114 名患者(80.8%)在住院期间至少遇到了一种潜在的药物-药物相互作用。从机制上讲,大多数药物-药物相互作用(56.4%)是药效学相互作用。格拉司琼和甲氧氯普胺之间的相互作用是检测到的前 10 种相互作用之一(占总药物-药物相互作用的 11.4%)。多西他赛和卡铂之间的相互作用是肿瘤药物中最常见的药物-药物相互作用(占总药物-药物相互作用的 2.6%)。
实体瘤癌症患者中经常发生潜在的中度或重度药物-药物相互作用,需要建立临床药学服务,提供相关的药物治疗咨询,以防止这一潜在的严重问题。