Departments of Clinical Research.
Infectious Disease and Vaccine Research; and.
J Acquir Immune Defic Syndr. 2020 Dec 15;85(5):635-642. doi: 10.1097/QAI.0000000000002496.
Doravirine (DOR) is a novel non-nucleoside reverse transcriptase inhibitor (NNRTI) approved for the treatment of HIV-1 infection in patients with no known DOR resistance-associated mutations. DOR was rationally designed to address limitations associated with other approved NNRTIs, particularly resistance from common NNRTI resistance-associated mutants containing K103N, Y181C, or G190A reverse transcriptase substitutions.
Data to date from both in vitro studies and clinical trials have been compiled to summarize the resistance profile of DOR.
We analyzed data from in vitro studies and phase 2 and 3 trials to assess the emergence of resistance-associated mutations and their impact on efficacy among participants treated with DOR.
DOR exhibited a distinct resistance profile compared with efavirenz and rilpivirine in vitro and in vivo; mutant viruses that were resistant to DOR showed limited cross-resistance to efavirenz and rilpivirine. In clinical trials, the development of DOR resistance-associated substitutions in reverse transcriptase was uncommon.
Overall, minimal cross-resistance across NNRTIs was observed for DOR and limited development of DOR-related resistance. These data should assist clinicians in further understanding the resistance profile of DOR, so appropriate treatment decisions can be made for their patients.
多伟拉韦(DOR)是一种新型非核苷类逆转录酶抑制剂(NNRTI),获批用于治疗无已知 DOR 耐药相关突变的 HIV-1 感染患者。DOR 是经过合理设计的,旨在解决其他已批准的 NNRTI 存在的局限性,尤其是针对常见 NNRTI 耐药相关突变体(包含 K103N、Y181C 或 G190A 逆转录酶取代)引起的耐药问题。
目前已汇总了来自体外研究和临床试验的数据,以总结 DOR 的耐药谱。
我们分析了来自体外研究和 2 期和 3 期临床试验的数据,以评估 DOR 治疗参与者中耐药相关突变的出现及其对疗效的影响。
与体外和体内的依非韦伦和利匹韦林相比,DOR 表现出独特的耐药谱;对 DOR 耐药的突变病毒对依非韦伦和利匹韦林的交叉耐药性有限。在临床试验中,逆转录酶中 DOR 耐药相关取代的出现并不常见。
总体而言,DOR 与 NNRTI 之间交叉耐药性最小,与 DOR 相关的耐药性发展有限。这些数据应有助于临床医生进一步了解 DOR 的耐药谱,以便为患者做出适当的治疗决策。