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多替拉韦真实世界研究:初治 HIV-1 患者中多替拉韦联合拉米夫定(48 周)。

DOLAVI Real-Life Study of Dolutegravir Plus Lamivudine in Naive HIV-1 Patients (48 Weeks).

机构信息

Unit of Infectious Diseases, Virgen de las Nieves University Hospital, 18014 Granada, Spain.

Unit of Infectious Diseases, University Hospital San Cecilio, 18016 Granada, Spain.

出版信息

Viruses. 2022 Mar 4;14(3):524. doi: 10.3390/v14030524.

Abstract

Brief: Real-world data in naïve HIV-1 patients demonstrate that dolutegravir plus lamivudine in a multiple tablet regimen is effective, safe, and satisfactory; it causes moderately increasing weight and abdominal circumference and is administrable on a test-and-treat strategy. Background: Our objectives were to determine the real-life effectiveness and safety of DT with dolutegravir (50 mg/QD) plus lamivudine (300 mg/QD) in a multiple-tablet regimen (MTR) in naïve PLHIV followed up for 48 weeks and to evaluate the compliance and satisfaction of patients. Material and methods: An open, single-arm, multicenter, non-randomized clinical trial from May 2019 through September 2020 with a 48-week follow-up. Results: The study included 88 PLHIV patients (87.5% male) with a mean age of 35.9 years; 76.1% were MSM patients. The mean baseline CD4 was 516.4 cells/uL, with a viral load (VL) of 4.49 log10, and 11.4% were in the AIDS stage. DT started within 7 days of first specialist consultation in all patients and the same day in 84.1%; 3.4% had baseline resistance mutations (K103N, V106I + E138A, and V108I); 12.5% were lost to follow-up. At week 48, 86.3% had VL < 50 cop/uL by intention-to-treat analysis and 98.7% by per-protocol (PP) analysis. Virological failure (VF) was recorded in 1.1%, with no resistance mutation. One blip was detected in 5.2% without VF. Three reported anxiety, dizziness, and cephalgia, respectively, at week 4 and one reported insomnia at week 24; none reported adverse events at week 48. The mean weight was 4 kg higher at 48 weeks (p = 0.0001) and abdominal circumference 3 cm larger at 24 weeks (p = 0.022). No forgetfulness occurred in 98.7% of patients. Patient satisfaction was 90/100 at 4, 24, and 48 weeks. Conclusion: Real-world data demonstrate that dolutegravir plus lamivudine in MTR is effective, safe, and satisfactory, moderately increasing weight and abdominal circumference and administrable on a test-and-treat strategy.

摘要

简介

在初治 HIV-1 患者的真实世界数据中,证实了多替拉韦加拉米夫定复方片剂(DTG 50mg/每日一次+拉米夫定 300mg/每日一次)在多种片剂方案(MTR)中的有效性、安全性和满意度;该方案会导致体重和腹围适度增加,且可采用检测和治疗策略。背景:我们的目标是确定初治 PLHIV 采用多替拉韦加拉米夫定复方片剂(DTG 50mg/每日一次+拉米夫定 300mg/每日一次)在 MTR 中的真实世界疗效和安全性,该研究为期 48 周,同时评估患者的依从性和满意度。材料与方法:这是一项 2019 年 5 月至 2020 年 9 月进行的、开放性、单臂、多中心、非随机临床试验,随访 48 周。结果:该研究纳入了 88 例初治 PLHIV 患者(87.5%为男性),平均年龄 35.9 岁;76.1%为男男性行为者。平均基线 CD4 为 516.4 个细胞/μL,病毒载量(VL)为 4.49 log10,11.4%处于艾滋病期。所有患者均在首次专科就诊后 7 天内(84.1%在同一天)开始使用 DTG,3.4%患者存在基线耐药突变(K103N、V106I+E138A 和 V108I),12.5%患者失访。48 周时,86.3%的患者按意向治疗分析和 98.7%的按方案分析(PP)达到 VL<50cop/uL。记录到 1.1%的病毒学失败(VF),无耐药突变。5.2%的患者检测到 1 次峰值,无 VF。3 例患者分别在第 4 周报告了焦虑、头晕和头痛,1 例患者在第 24 周报告了失眠;48 周时,没有患者报告不良事件。48 周时体重平均增加 4kg(p=0.0001),24 周时腹围平均增加 3cm(p=0.022)。98.7%的患者没有遗忘。患者满意度在第 4、24 和 48 周时均为 90/100。结论:真实世界数据表明,多替拉韦加拉米夫定复方片剂在 MTR 中有效、安全且令人满意,会适度增加体重和腹围,且可采用检测和治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9235/8951045/f1f2058a7fc6/viruses-14-00524-g001.jpg

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