Agnihotri Akash, Ramasubbu Saravana Kumar, Bandyopadhyay Arkapal, Bidarolli Manjunath, Nath Uttam Kumar, Das Biswadeep
Department of Pharmacology, Amrita School of Medicine, Faridabad, IND.
Department of Pharmacology, Andaman and Nicobar Islands Institute of Medical Sciences, Port Blair, IND.
Cureus. 2024 May 17;16(5):e60492. doi: 10.7759/cureus.60492. eCollection 2024 May.
Introduction Cancer chemotherapy regimens include multiple classes of adjuvant drugs as supportive therapy. Because of the concurrent intake of other drugs (like antiemetics, antidepressants, analgesics, and antimicrobials), there is a heightened risk for possible QT interval prolongation. There is a dearth of evidence in the literature regarding the usage of QT-prolonging anticancer drugs and associated risk factors that have the propensity to prolong QT interval. The purpose was to explore the extent of the use of QT-interval-prolonging drugs and potential QT-prolonging drug-drug interactions (QT-DDIs) in cancer patients attending OPD in a tertiary-care hospital. Methods This was a hospital-based, cross-sectional, observational study. Risk stratification of QT-prolonging drugs for torsades de pointes (TdP) was done by the Arizona Center for Education and Research on Therapeutics (AzCERT)/CredibleMeds-lists, and potential QT-DDIs were determined with four online DDI-checker-software. Results In 1331 cancer patients, the overall prevalence of potential QT-prolonging drug utilization was 97.3%. Ondansetron, pantoprazole, domperidone, and olanzapine were the most frequent QT-prolonging drugs in cancer patients. The top six antineoplastics with potential QT-prolonging and torsadogenic actions were capecitabine, oxaliplatin, imatinib, bortezomib, 5-fluorouracil, and bendamustine. Evidence-based pragmatic QTc interval prolongation risk assessment tools are imperative for cancer patients. Conclusion This study revealed a high prevalence of QT-prolonging drugs and QT-DDIs among cancer patients who are treated with anticancer and non-anticancer drugs. As a result, it's critical to take precautions, stay vigilant, and avoid QT-prolonging in clinical situations. Evidence-based pragmatic QTc interval prolongation risk assessment tools are needed for cancer patients.
引言 癌症化疗方案包括多种辅助药物作为支持性治疗。由于同时服用其他药物(如止吐药、抗抑郁药、镇痛药和抗菌药),QT间期延长的风险增加。文献中缺乏关于延长QT间期的抗癌药物使用情况以及具有延长QT间期倾向的相关危险因素的证据。目的是探讨在一家三级医院门诊就诊的癌症患者中使用延长QT间期药物的程度以及潜在的延长QT间期的药物相互作用(QT-DDI)。方法 这是一项基于医院的横断面观察性研究。通过亚利桑那治疗教育与研究中心(AzCERT)/可信药物清单对延长QT间期药物致尖端扭转型室速(TdP)进行风险分层,并使用四款在线药物相互作用检查软件确定潜在的QT-DDI。结果 在1331例癌症患者中,潜在延长QT间期药物使用的总体患病率为97.3%。昂丹司琼、泮托拉唑、多潘立酮和奥氮平是癌症患者中最常用的延长QT间期药物。具有潜在延长QT间期和致TdP作用的前六种抗肿瘤药是卡培他滨、奥沙利铂、伊马替尼、硼替佐米、5-氟尿嘧啶和苯达莫司汀。基于证据的实用QTc间期延长风险评估工具对癌症患者至关重要。结论 本研究揭示了在接受抗癌和非抗癌药物治疗的癌症患者中,延长QT间期药物和QT-DDI的高患病率。因此,在临床情况下采取预防措施、保持警惕并避免QT间期延长至关重要。癌症患者需要基于证据的实用QTc间期延长风险评估工具。