Office of Clinical Pharmacology, Office of Translational Sciences, Center for Drug Evaluation and Review, Food and Drug Administration, Silver Spring, MD, USA.
Office of Pharmacovigilance and Epidemiology, Office of Surveillance and Epidemiology, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD, USA.
J Clin Pharmacol. 2019 Apr;59(4):500-509. doi: 10.1002/jcph.1345. Epub 2018 Nov 19.
Although current quetiapine labeling recommends that its dosage should be lowered 6-fold when coadministered with strong cytochrome P450 (CYP)3A inhibitors, a reported case of coma in a patient receiving quetiapine with lopinavir and ritonavir prompted the reevaluation of labeling recommendations for the dosing of quetiapine when coadministered with human immunodeficiency virus (HIV) protease inhibitors. Literature and database (FDA Adverse Event Reporting System and United States Symphony Health Solutions' Integrated Dataverse Database) searches allowed us to identify cases of coma and related adverse events involving the coadministration of quetiapine and HIV protease inhibitors and to estimate the frequency of concomitant use. Literature review and physiologically based pharmacokinetic modeling allowed us to estimate the potential for CYP3A inhibition to contribute to adverse events related to HIV protease inhibitor-quetiapine coadministration. We identified excess sedation following coadministration of quetiapine and an HIV protease inhibitor in 3 reports without obvious confounders. In prescription claims data, 0.4% of quetiapine patients were dispensed a concurrent ritonavir prescription. The quetiapine dose was not reduced on ritonavir initiation in 90% of therapy episodes. Available data indicate to us that all HIV protease inhibitors combined with ritonavir are likely to be strong CYP3A inhibitors. We predicted that ritonavir would increase quetiapine exposure comparable to the strong CYP3A inhibitor ketoconazole. The current dosing recommendations for use of quetiapine with strong CYP3A inhibitors (ie, 6-fold lower quetiapine dose) are appropriate and should be followed when quetiapine is coadministered with HIV protease inhibitors.
虽然目前的喹硫平说明书建议,当与强细胞色素 P450(CYP)3A 抑制剂合用时,应将其剂量降低 6 倍,但有报道称,在接受洛匹那韦和利托那韦联合治疗的患者中,出现昏迷,这促使人们重新评估喹硫平与人类免疫缺陷病毒(HIV)蛋白酶抑制剂合用时的剂量建议。文献和数据库(FDA 不良事件报告系统和美国 Symphony Health Solutions 的综合数据数据库)搜索使我们能够确定涉及喹硫平与 HIV 蛋白酶抑制剂联合用药的昏迷和相关不良事件的病例,并估计合并用药的频率。文献复习和基于生理学的药代动力学模型使我们能够估计 CYP3A 抑制对与 HIV 蛋白酶抑制剂-喹硫平联合用药相关不良事件的潜在影响。我们在 3 份报告中发现,在合并使用喹硫平和 HIV 蛋白酶抑制剂后,出现了过度镇静,且没有明显的混杂因素。在处方索赔数据中,0.4%的喹硫平患者同时开具了利托那韦处方。在 90%的治疗期间,利托那韦起始时未降低喹硫平剂量。现有数据表明,所有与利托那韦联合使用的 HIV 蛋白酶抑制剂都可能是强 CYP3A 抑制剂。我们预测,利托那韦会增加喹硫平的暴露,与强 CYP3A 抑制剂酮康唑相当。目前使用强 CYP3A 抑制剂(即降低 6 倍喹硫平剂量)的喹硫平建议剂量是合适的,当喹硫平与 HIV 蛋白酶抑制剂合用时,应遵循这些建议。