Tseng Alice, Hughes Christine A, Wu Janet, Seet Jason, Phillips Elizabeth J
1 Toronto General Hospital, Toronto, Canada.
2 University of Alberta, Edmonton, AB, Canada.
Ann Pharmacother. 2017 Nov;51(11):1008-1022. doi: 10.1177/1060028017717018. Epub 2017 Jun 19.
To describe properties of cobicistat and ritonavir; compare boosting data with atazanavir, darunavir, and elvitegravir; and summarize antiretroviral and comedication interaction studies, with a focus on similarities and differences between ritonavir and cobicistat. Considerations when switching from one booster to another are discussed.
A literature search of MEDLINE was performed (1985 to April 2017) using the following search terms: cobicistat, ritonavir, pharmacokinetic, drug interactions, booster, pharmacokinetic enhancer, HIV, antiretrovirals. Abstracts from conferences, article bibliographies, and product monographs were reviewed.
Relevant English-language studies or those conducted in humans were considered.
Similar exposures of elvitegravir, darunavir, and atazanavir are achieved when combined with cobicistat or ritonavir. Cobicistat may not be as potent a CYP3A4 inhibitor as ritonavir in the presence of a concomitant inducer. Ritonavir induces CYP1A2, 2B6, 2C9, 2C19, and uridine 5'-diphospho-glucuronosyltransferase, whereas cobicistat does not. Therefore, recommendations for cobicistat with comedications that are extrapolated from studies using ritonavir may not be valid. Pharmacokinetic properties of the boosted antiretroviral can also affect interaction outcome with comedications. Problems can arise when switching patients from ritonavir to cobicistat regimens, particularly with medications that have a narrow therapeutic index such as warfarin.
When assessing and managing potential interactions with ritonavir- or cobicistat-based regimens, clinicians need to be aware of important differences and distinctions between these agents. This is especially important for patients with multiple comorbidities and concomitant medications. Additional monitoring or medication dose adjustments may be needed when switching from one booster to another.
描述考比司他和利托那韦的特性;比较其与阿扎那韦、达芦那韦和埃替格韦的增效数据;总结抗逆转录病毒药物及合并用药的相互作用研究,重点关注利托那韦和考比司他之间的异同。讨论从一种增效剂换用另一种增效剂时的注意事项。
使用以下检索词对MEDLINE进行文献检索(1985年至2017年4月):考比司他、利托那韦、药代动力学、药物相互作用、增效剂、药代动力学增强剂、HIV、抗逆转录病毒药物。对会议摘要、文章参考文献和产品说明书进行了审查。
考虑相关的英文研究或在人体中进行的研究。
埃替格韦、达芦那韦和阿扎那韦与考比司他或利托那韦联用时可达到相似的暴露水平。在有同时使用的诱导剂存在时,考比司他作为CYP3A4抑制剂的效力可能不如利托那韦。利托那韦可诱导CYP1A2、2B6、2C9、2C19和尿苷5'-二磷酸葡萄糖醛酸转移酶,而考比司他则不能。因此,从使用利托那韦的研究中推断出的考比司他与合并用药的建议可能无效。增效后的抗逆转录病毒药物的药代动力学特性也可能影响与合并用药的相互作用结果。当患者从利托那韦治疗方案换用考比司他治疗方案时可能会出现问题,尤其是对于治疗指数较窄的药物,如华法林。
在评估和管理与基于利托那韦或考比司他的治疗方案的潜在相互作用时,临床医生需要了解这些药物之间的重要差异。这对于患有多种合并症和同时使用多种药物治疗的患者尤为重要。从一种增效剂换用另一种增效剂时可能需要额外的监测或调整药物剂量。