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

Author:

Orkin Chloe1ORCID,Schapiro Jonathan M2,Perno Carlo F3,Kuritzkes Daniel R4,Patel Parul5,DeMoor Rebecca6,Dorey David7,Wang Yongwei5,Han Kelong6,Van Eygen Veerle8,Crauwels Herta8,Ford Susan L9,Latham Christine L5,St. Clair Marty5,Polli Joseph W5,Vanveggel Simon8,Vandermeulen Kati8,D’Amico Ronald5,Garges Harmony P5,Zolopa Andrew5,Spreen William R5,van Wyk Jean10,Cutrell Amy G5

Affiliation:

1. SHARE Collaborative, Department of Immunobiology, Queen Mary University of London , London , United Kingdom

2. National Hemophilia Center, Sheba Medical Center , Ramat Gan , Israel

3. IRCCS Bambino Gesù Pediatric Hospital , Rome , Italy

4. Division of Infectious Diseases, Brigham and Women’s Hospital, Harvard Medical School , Boston, Massachusetts , USA

5. ViiV Healthcare , Durham, North Carolina , USA

6. GSK , Collegeville, Pennsylvania , USA

7. GSK , Mississauga , Canada

8. Janssen Research & Development , Beerse , Belgium

9. GSK , Durham, North Carolina , USA

10. ViiV Healthcare , Brentford , United Kingdom

Abstract

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/m2 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/m2) 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.

Funder

ViiV Healthcare

Janssen Pharmaceuticals

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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