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长效注射用卡博特韦/利匹韦林治疗的HIV感染青少年和青年的疗效、安全性及治疗依从性:真实世界观察性队列研究结果

Efficacy, Safety and Retention in Care Among Adolescents and Youth With HIV on Long-acting Injectable Cabotegravir/Rilpivirine Treatment: Real-world Observational Cohort Outcomes.

作者信息

Williams Tierra, Unternaher Justin, Koay Wei Li Adeline, Anderson Lorato, Bright Kimberly, Mareuil Joanna, Rakhmanina Natella

机构信息

From the Division of Infectious Diseases.

Division of Infectious Diseases, Department of Pediatrics, Medical University of South Carolina, Charleston, SC.

出版信息

Pediatr Infect Dis J. 2025 Jan 24;44(7):650-656. doi: 10.1097/INF.0000000000004742.

Abstract

BACKGROUND

Long-acting injectable (LAI) cabotegravir/rilpivirine (CAB/RPV) can improve adherence among adolescents and youth with HIV (AYHIV). We evaluated LAI CAB/RPV treatment outcomes among AYHIV.

METHODS

An observational cohort study of AYHIV <25 years initiated LAI CAB/RPV from October 2021 to June 2024 as a standard of care. Descriptive data included demographics (age, race/ethnicity and gender/sexual orientation), body mass index, HIV history, efficacy (CD4, HIV RNA and resistance), safety and retention in care.

RESULTS

Twenty-five AYHIV (48% cisgender females; median age, 19 years; 64% with perinatally acquired HIV; median body mass index = 25.3 kg/m 2 ; 52% virally suppressed for ≥6 months) received LAI CAB/RPV for a median duration of 11.8 (range, 0.8-31.3) months. Majority (n=24; 96%) initiated monthly LAI CAB/RPV injections, and 19 AYHIV (76%) switched to bimonthly injections. Seven AYHIV (28%) experienced transient viremia episodes (1-5/person; ranges, 48-1100 copies/mL) with most (78%) occurring within the initial 12 months, all episodes resolved at retesting after 3 to 91 days and none resulted in CAB and/or RPV resistance. Injection-associated pain/discomfort was mild to moderate and decreased over time. Grade 2 adverse events were self-resolved and included 3 AYHIV with postinjection adverse reactions and 1 AYHIV with QTc prolongation. Three cisgender female AYHIV became pregnant and continued LAI CAB/RPV. There were no discontinuations, missed or delayed injections. All AYHIV were virally suppressed at the end of the study follow-up.

CONCLUSIONS

We report 100% engagement in care and viral suppression among 25 AYHIV on LAI CAB/RPV during study follow-up. More data are needed to evaluate the long-term outcomes and sustainability of LAI CAB/RPV treatment in AYHIV.

摘要

背景

长效注射用卡博特韦/利匹韦林(CAB/RPV)可提高感染艾滋病毒的青少年和青年(AYHIV)的依从性。我们评估了AYHIV中长效注射用CAB/RPV的治疗效果。

方法

一项对25岁以下AYHIV的观察性队列研究,于2021年10月至2024年6月开始将长效注射用CAB/RPV作为标准治疗方法。描述性数据包括人口统计学特征(年龄、种族/民族和性别/性取向)、体重指数、艾滋病毒病史、疗效(CD4、艾滋病毒核糖核酸和耐药性)、安全性以及护理依从性。

结果

25名AYHIV(48%为顺性别女性;中位年龄19岁;64%为围产期感染艾滋病毒;中位体重指数=25.3kg/m²;52%病毒抑制≥6个月)接受长效注射用CAB/RPV,中位持续时间为11.8(范围0.8 - 31.3)个月。大多数(n = 24;96%)开始每月注射长效注射用CAB/RPV,19名AYHIV(76%)改为每两个月注射一次。7名AYHIV(28%)经历了短暂病毒血症发作(每人1 - 5次;范围48 - 1100拷贝/毫升),大多数(78%)发生在最初12个月内,所有发作在3至91天后复查时消退,且无一导致CAB和/或RPV耐药。注射相关疼痛/不适为轻至中度,且随时间减轻。2级不良事件自行缓解,包括3名有注射后不良反应的AYHIV和1名QTc延长的AYHIV。3名顺性别女性AYHIV怀孕并继续使用长效注射用CAB/RPV。无停药、漏注或延迟注射情况。在研究随访结束时,所有AYHIV均实现病毒抑制。

结论

我们报告在研究随访期间,25名接受长效注射用CAB/RPV治疗的AYHIV的护理依从性和病毒抑制率均达100%。需要更多数据来评估长效注射用CAB/RPV治疗AYHIV的长期效果和可持续性。

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