Unit of Infectious Diseases, Virgen de las Nieves University Hospital, 18014 Granada, Spain.
Unit of Infectious Diseases, University Hospital San Cecilio, 18016 Granada, Spain.
Viruses. 2022 Mar 4;14(3):524. doi: 10.3390/v14030524.
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.
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。