Chen Wanyi, Gandhi Monica, Sax Paul E, Neilan Anne M, Garland Wendy H, Wilkin Timothy, Cohen Rebecca, Ciaranello Andrea L, Kulkarni Sonali P, Eron Joseph, Freedberg Kenneth A, Hyle Emily P
Medical Practice Evaluation Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Division of HIV, Infectious Diseases, and Global Medicine, University of California, San Francisco, San Francisco, California, USA.
Open Forum Infect Dis. 2023 Jul 22;10(8):ofad390. doi: 10.1093/ofid/ofad390. eCollection 2023 Aug.
In a demonstration project, long-acting, injectable cabotegravir-rilpivirine (CAB-RPV) achieved viral suppression in a high proportion of people with HIV (PWH) who were virologically nonsuppressed with adherence barriers. We projected the long-term impact of CAB-RPV for nonsuppressed PWH experiencing adherence barriers.
Using the Cost-Effectiveness of Preventing AIDS Complications (CEPAC) model, we compared 3 strategies: (1) standard of care oral integrase inhibitor-based ART (); (2) INSTI-based ART with supportive social services ("wraparound services" [WS]) (); and (3) CAB-RPV with WS (). Model outcomes included viral suppression (%) and engagement in care (%) at 3 years, and life expectancy (life-years [LYs]). Base case cohort characteristics included mean age of 47y (standard deviation [SD], 10y), 90% male at birth, and baseline mean CD4 count 150/µL (SD, 75/µL). Viral suppression at 3 months was 13% (), 28% (), and 60% (). Mean loss to follow-up was 28/100 person-years (PY) (SD, 2/100 PY) without WS and 16/100 PY (SD, 1/100 PY) with WS.
Projected viral suppression at 3 years would vary widely: 16% (), 38% (), and 44% (). Life expectancy would be 7.4 LY (), 9.0 LY (), and 9.4 LY (). Projected benefits over oral ART would be greater for PWH initiating at lower CD4 counts. Across plausible key parameter ranges, would improve viral suppression and life expectancy compared with oral INSTI strategies.
These model-based results support that long-acting injectable CAB-RPV with extensive support services for nonsuppressed PWH experiencing adherence barriers is likely to increase viral suppression and improve survival. A prospective study to provide further evidence is needed.
在一个示范项目中,长效注射用卡博特韦-利匹韦林(CAB-RPV)在很大一部分因依从性障碍而病毒学未得到抑制的艾滋病毒感染者(PWH)中实现了病毒抑制。我们预测了CAB-RPV对经历依从性障碍的病毒学未得到抑制的PWH的长期影响。
使用预防艾滋病并发症成本效益(CEPAC)模型,我们比较了3种策略:(1)基于口服整合酶抑制剂的标准治疗方案();(2)基于整合酶链转移抑制剂(INSTI)的抗逆转录病毒治疗(ART)并提供支持性社会服务(“综合服务”[WS])();以及(3)CAB-RPV联合WS()。模型结果包括3年时的病毒抑制率(%)和治疗参与率(%),以及预期寿命(生命年[LYs])。基础病例队列特征包括平均年龄47岁(标准差[SD],10岁),90%为出生时男性,基线平均CD4细胞计数150/µL(SD,75/µL)。3个月时的病毒抑制率分别为13%()、28%()和60%()。无WS时平均失访率为28/100人年(PY)(SD,2/100 PY),有WS时为16/100 PY(SD,1/100 PY)。
预测3年时的病毒抑制率差异很大:分别为16%()、38%()和44%()。预期寿命分别为7.4生命年()、9.0生命年()和9.4生命年()。对于CD4细胞计数较低时开始治疗的PWH,与口服ART相比,预测的益处更大。在合理的关键参数范围内,与口服INSTI策略相比,CAB-RPV联合WS将提高病毒抑制率和预期寿命。
这些基于模型的结果支持,对于经历依从性障碍的病毒学未得到抑制的PWH,长效注射用CAB-RPV并提供广泛支持服务可能会提高病毒抑制率并改善生存率。需要进行前瞻性研究以提供进一步的证据。