Transient Viremia Among People with HIV Receiving Injectable Cabotegravir Plus Rilpivirine

被引:0
|
作者
O'Connor, Lauren F. [1 ]
Koay, Wei Li Adeline [2 ,3 ]
Unternaher, Justin [2 ]
Byrne, Morgan [1 ]
Monroe, Anne K. [1 ]
Greenberg, Alan [1 ]
Castel, Amanda D. [1 ]
Rakhmanina, Natella [2 ,4 ,5 ]
DC Cohort Executive Comm
机构
[1] George Washington Univ, Milken Inst, Sch Publ Hlth, Washington, DC USA
[2] Childrens Natl Hosp, Div Infect Dis, 111 Michigan Ave NW,West Wing Level 3 5,Suite 100, Washington, DC 20010 USA
[3] Med Univ South Carolina, Dept Pediat, Charleston, SC USA
[4] George Washington Univ, Sch Med & Hlth Sci, Dept Pediat, Washington, DC USA
[5] Elizabeth Glaser Pediat AIDS Fdn, Washington, DC USA
关键词
HIV; cabotegravir-rilpivirine; injectable; viremia; long-acting; LONG-ACTING CABOTEGRAVIR; THERAPY; CHALLENGES; ADULTS;
D O I
10.1089/aid.2024.0083
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Long-acting injectable (LAI) cabotegravir/rilpivirine (CAB/RPV) provides an effective treatment option for people with HIV (PWH). Studies suggest that PWH on LAI CAB/RPV may experience isolated episodes of transient viremia (HIV RNA > 20 copies/mL) defined as virologic blips (VB). The risk factors for VB in PWH receiving LAI CAB/RPV are limited. We aimed to describe a cohort of PWH on LAI CAB/RPV and evaluate risk factors and time to VB following LAI CAB/RPV initiation. We obtained DC Cohort data from PWH who initiated LAI CAB/RPV prior to July 2023 and used Kaplan-Meier curves and Cox proportional hazards models to evaluate the association between participant demographics, HIV clinical factors, and time to VB. Among 98 PWH who initiated LAI CAB/RPV, 9 (9.2%) experienced at least one VB (median HIV RNA = 50 copies/mL; ranges 30-12,000 copies/mL) during a median follow-up period of five months (IQR: 2-10). The median CD4 count among PWH was 754 cells/mL (IQR: 598, 980) at the time of LAI CAB/RPV initiation. Having a high CD4 (>= 500 cells/lL) at LAI CAB/RPV initiation was significantly associated with a lower hazard for VB when compared to baseline CD4 < 200 cells/mL [hazard ratios (HR): 0.15 [95% confidence intervals (CI): 0.03, 0.77]; aHR: 0.07 (95% CI: 0.01, 0.50); log-rank p = .026]. No other characteristics were significantly associated with time to VB, and no participants experienced virologic failure. Considerations for baseline CD4 may be important when initiating a patient on LAI CAB/RPV, and future studies will help evaluate the VB occurrence and associated factors among PWH.
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