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多替拉韦/拉米夫定单片方案:HIV-1 感染治疗的综述。

Dolutegravir/Lamivudine Single-Tablet Regimen: A Review in HIV-1 Infection.

机构信息

Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.

出版信息

Drugs. 2020 Jan;80(1):61-72. doi: 10.1007/s40265-019-01247-1.

Abstract

The oral once-daily, fixed-dose single-tablet regimen (STR) of dolutegravir/lamivudine (Dovato), combining a second generation integrase single-strand transfer inhibitor (INSTI) and a nucleoside reverse transcriptase inhibitor (NRTI), is indicated as a complete regimen for the treatment of HIV-1 infection in adults and adolescents (> 12 years of age weighing at least 40 kg) with no known or suspected resistance to the INSTI class or lamivudine. In GEMINI trials in antiretroviral therapy (ART)-naïve HIV-1-infected adults, treatment with dolutegravir plus lamivudine provided rapid and sustained virological suppression and was noninferior to dolutegravir plus tenofovir disoproxil fumarate/emtricitabine at 48 weeks, irrespective of baseline patient or disease characteristics. Virological suppression was sustained at 96 weeks in these ongoing trials. In patients with HIV-1 with sustained virological suppression on their current tenofovir alafenamide (AF)-based ART regimen (≥ 3 drugs), switching to treatment with dolutegravir/lamivudine was noninferior to continuing on a tenofovir AF-based regimen at 48 weeks in the ongoing TANGO trial. No resistance mutations to dolutegravir or lamivudine were detected in patients who met criteria for confirmed virological withdrawal in GEMINI and TANGO trials. Hence, the dolutegravir/lamivudine STR is an effective, generally well tolerated and convenient initial and subsequent ART option for adolescents and adults with HIV-1 infection with no known or suspected resistance to the INSTI class or lamivudine.

摘要

多替拉韦/拉米夫定(Dovato)的每日口服、固定剂量单一片剂方案(STR),结合了第二代整合酶单链转移抑制剂(INSTI)和核苷逆转录酶抑制剂(NRTI),适用于治疗成人和青少年(≥12 岁且体重至少 40kg)的 HIV-1 感染,这些患者对 INSTI 类药物或拉米夫定无已知或疑似耐药。在 GEMINI 临床试验中,初治 HIV-1 感染成人患者接受多替拉韦加拉米夫定治疗可快速且持续抑制病毒,在第 48 周时与多替拉韦加富马酸替诺福韦二吡呋酯/恩曲他滨相比非劣效,无论基线患者或疾病特征如何。在这些正在进行的试验中,病毒学抑制在第 96 周时仍持续。在当前基于替诺福韦艾拉酚胺(AF)的 ART 方案(≥3 种药物)下病毒学抑制持续的 HIV-1 患者中,在 TANGO 试验中,转换为多替拉韦/拉米夫定治疗在第 48 周时与继续基于替诺福韦 AF 的方案相比非劣效。在 GEMINI 和 TANGO 试验中符合确认病毒学停药标准的患者中,未检测到对多替拉韦或拉米夫定的耐药突变。因此,多替拉韦/拉米夫定 STR 是一种有效、一般耐受良好且方便的初始和后续 ART 选择,适用于对 INSTI 类药物或拉米夫定无已知或疑似耐药的 HIV-1 感染的青少年和成人。

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