Department of Pharmacy Practice, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, India.
Department of Pharmacy Practice, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, India.
Arch Med Res. 2021 Apr;52(3):261-269. doi: 10.1016/j.arcmed.2020.11.006. Epub 2020 Nov 17.
Lung cancer patients are at heightened risk for developing COVID-19 infection as well as complications due to multiple risk factors such as underlying malignancy, anti-cancer treatment induced immunosuppression, additional comorbidities and history of smoking. Recent literatures have reported a significant proportion of lung cancer patients coinfected with COVID-19. Chloroquine, hydroxychloroquine, lopinavir/ritonavir, ribavirin, oseltamivir, remdesivir, favipiravir, and umifenovir represent the major repurposed drugs used as potential experimental agents for COVID-19 whereas azithromycin, dexamethasone, tocilizumab, sarilumab, famotidine and ceftriaxone are some of the supporting agents that are under investigation for COVID-19 management. The rationale of this review is to identify potential drug-drug interactions (DDIs) occurring in lung cancer patients receiving lung cancer medications and repurposed COVID-19 drugs using Micromedex and additional literatures. This review has identified several potential DDIs that could occur with the concomitant treatments of COVID-19 repurposed drugs and lung cancer medications. This information may be utilized by the healthcare professionals for screening and identifying potential DDIs with adverse outcomes, based on their severity and documentation levels and consequently design prophylactic and management strategies for their prevention. Identification, reporting and management of DDIs and dissemination of related information should be a major consideration in the delivery of lung cancer care during this ongoing COVID-19 pandemic for better patient outcomes and updating guidelines for safer prescribing practices in this coinfected condition.
肺癌患者由于多种风险因素,如潜在恶性肿瘤、抗癌治疗引起的免疫抑制、合并症和吸烟史,感染 COVID-19 以及发生并发症的风险增加。最近的文献报道了相当一部分肺癌患者同时感染了 COVID-19。氯喹、羟氯喹、洛匹那韦/利托那韦、利巴韦林、奥司他韦、瑞德西韦、法匹拉韦和乌米酚是用于 COVID-19 的主要重新利用药物,而阿奇霉素、地塞米松、托珠单抗、沙利鲁单抗、法莫替丁和头孢曲松是正在研究用于 COVID-19 管理的一些支持药物。本综述的目的是使用 Micromedex 和其他文献,确定接受肺癌药物和重新利用 COVID-19 药物治疗的肺癌患者中发生的潜在药物相互作用 (DDI)。本综述确定了几种潜在的 DDI,这些 DDI 可能与 COVID-19 重新利用药物和肺癌药物的联合治疗同时发生。根据严重程度和记录级别,这些信息可由医疗保健专业人员用于筛查和识别潜在的 DDI 及其不良后果,并相应地设计预防和管理策略以预防它们。在 COVID-19 大流行期间,在提供肺癌护理时,应高度重视识别、报告和管理 DDI 以及传播相关信息,以改善患者的结局并更新针对这种合并感染的更安全处方实践的指南。