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艾维雷韦/考比司他/恩曲他滨/替诺福韦酯富马酸单片复方制剂(Stribild®):在成人 HIV-1 感染管理中的应用评价。

Elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil fumarate single-tablet regimen (Stribild®): a review of its use in the management of HIV-1 infection in adults.

机构信息

Adis, 41 Centorian Drive, Private Bag 65901, Mairangi Bay, North Shore, 0754, Auckland, New Zealand,

出版信息

Drugs. 2014 Jan;74(1):75-97. doi: 10.1007/s40265-013-0158-4.

Abstract

A new single-tablet, fixed-dose formulation consisting of elvitegravir, an HIV-1 integrase strand transfer inhibitor (INSTI); cobicistat, a pharmacokinetic enhancer; emtricitabine, a nucleoside reverse transcriptase inhibitor; and tenofovir disoproxil fumarate (tenofovir DF), a nucleotide reverse transcriptase inhibitor (elvitegravir/cobicistat/emtricitabine/tenofovir DF 150 mg/150 mg/200 mg/300 mg; Stribild®) is available in some countries for the once-daily treatment of HIV-1 infection in antiretroviral therapy-naïve adults. Elvitegravir/cobicistat/emtricitabine/tenofovir DF is the first INSTI-based single-tablet regimen available for the complete initial treatment of adults with HIV-1 infection. In two large, randomized, double-blind, phase III trials, once-daily treatment with elvitegravir/cobicistat/emtricitabine/tenofovir DF was effective in reducing plasma HIV-1 RNA levels to <50 copies/mL at the week 48 assessment and showed virological efficacy noninferior to that of the efavirenz/emtricitabine/tenofovir DF single-tablet regimen or a once-daily regimen of atazanavir plus ritonavir (ritonavir-boosted atazanavir) plus the fixed-dose combination of emtricitabine/tenofovir DF. Elvitegravir/cobicistat/emtricitabine/tenofovir DF also showed durable efficacy in terms of achieving sustained suppression of HIV-1 RNA levels to <50 copies/mL for up to 144 weeks in both of the phase III trials. Elvitegravir/cobicistat/emtricitabine/tenofovir DF is an important addition to the group of simplified once-daily single-tablet regimens currently available for the effective treatment of HIV-1 infection in antiretroviral therapy-naïve patients and is among the preferred regimens recommended for use as initial treatment. It offers advantages over more complex multiple-tablet regimens that may impair treatment adherence, which is fundamental to the successful management of HIV-1 infection.

摘要

一种新的单一片剂、固定剂量配方,由艾维雷格、HIV-1 整合酶链转移抑制剂(INSTI);考比司他,一种药代动力学增强剂;恩曲他滨,核苷逆转录酶抑制剂;和富马酸替诺福韦二吡呋酯(替诺福韦酯),一种核苷酸逆转录酶抑制剂(艾维雷格/考比司他/恩曲他滨/替诺福韦酯 150mg/150mg/200mg/300mg;Stribild®),在一些国家可用于治疗初治的 HIV-1 感染的成人患者,每日一次。艾维雷格/考比司他/恩曲他滨/替诺福韦酯是首个基于 INSTI 的单一片剂方案,可用于初治成人 HIV-1 感染的完全初始治疗。在两项大型、随机、双盲、III 期临床试验中,艾维雷格/考比司他/恩曲他滨/替诺福韦酯每日一次治疗,在第 48 周评估时可有效降低血浆 HIV-1 RNA 水平至<50 拷贝/ml,并显示出与依非韦伦/恩曲他滨/替诺福韦酯单一片剂方案或阿扎那韦加利托那韦(利托那韦增强的阿扎那韦)加恩曲他滨/替诺福韦酯固定剂量组合相当的病毒学疗效非劣效性。在这两项 III 期临床试验中,艾维雷格/考比司他/恩曲他滨/替诺福韦酯还表现出持久的疗效,可在长达 144 周的时间内持续抑制 HIV-1 RNA 水平至<50 拷贝/ml。艾维雷格/考比司他/恩曲他滨/替诺福韦酯是目前用于治疗初治 HIV-1 感染的简化每日一次单一片剂方案组的重要补充,也是作为初始治疗的首选方案之一。它优于可能影响治疗依从性的更复杂的多片方案,而治疗依从性是成功管理 HIV-1 感染的基础。

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