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Expanded Multivariable Models to Assist Patient Selection for Long-Acting Cabotegravir + Rilpivirine Treatment: Clinical Utility of a Combination of Patient, Drug Concentration, and Viral Factors Associated With Virologic Failure.

Authors :
Orkin, Chloe
Schapiro, Jonathan M
Perno, Carlo F
Kuritzkes, Daniel R
Patel, Parul
DeMoor, Rebecca
Dorey, David
Wang, Yongwei
Han, Kelong
Eygen, Veerle Van
Crauwels, Herta
Ford, Susan L
Latham, Christine L
Clair, Marty St.
Polli, Joseph W
Vanveggel, Simon
Vandermeulen, Kati
D'Amico, Ronald
Garges, Harmony P
Zolopa, Andrew
Source :
Clinical Infectious Diseases; 11/15/2023, Vol. 77 Issue 10, p1423-1431, 9p
Publication Year :
2023

Abstract

Background Previously reported post hoc multivariable analyses exploring predictors of confirmed virologic failure (CVF) with cabotegravir + rilpivirine long-acting (CAB + RPV LA) were expanded to include data beyond week 48, additional covariates, and additional participants. Methods Pooled data from 1651 participants were used to explore dosing regimen (every 4 or every 8 weeks), demographic, viral, and pharmacokinetic covariates as potential predictors of CVF. Prior dosing regimen experience was accounted for using 2 populations. Two models were conducted in each population—baseline factor analyses exploring factors known at baseline and multivariable analyses exploring baseline factors plus postbaseline model-predicted CAB/RPV trough concentrations (4 and 44 weeks postinjection). Retained factors were evaluated to understand their contribution to CVF (alone or in combination). Results Overall, 1.4% (n = 23/1651) of participants had CVF through 152 weeks. The presence of RPV resistance-associated mutations, human immunodeficiency virus-1 subtype A6/A1, and body mass index ≥30 kg/m<superscript>2</superscript> were associated with an increased risk of CVF (P <.05 adjusted incidence rate ratio), with participants with ≥2 of these baseline factors having a higher risk of CVF. Lower model-predicted CAB/RPV troughs were additional factors retained for multivariable analyses. Conclusions The presence of ≥2 baseline factors (RPV resistance-associated mutations, A6/A1 subtype, and/or body mass index ≥30 kg/m<superscript>2</superscript>) was associated with increased CVF risk, consistent with prior analyses. Inclusion of initial model-predicted CAB/RPV trough concentrations (≤first quartile) did not improve the prediction of CVF beyond the presence of a combination of ≥2 baseline factors, reinforcing the clinical utility of the baseline factors in the appropriate use of CAB + RPV LA. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10584838
Volume :
77
Issue :
10
Database :
Complementary Index
Journal :
Clinical Infectious Diseases
Publication Type :
Academic Journal
Accession number :
173688234
Full Text :
https://doi.org/10.1093/cid/ciad370