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DOI 10.1093/cid/ciad370

Медицинская библиотека · Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023

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.

Orkin Chloe, Schapiro Jonathan M, Perno Carlo F, Kuritzkes Daniel R, Patel Parul, DeMoor Rebecca, Dorey David, Wang Yongwei, Han Kelong, Van Eygen Veerle, Crauwels Herta, Ford Susan L, Latham Christine L, St Clair Marty, Polli Joseph W, Vanveggel Simon, Vandermeulen Kati, D'Amico Ronald, Garges Harmony P, Zolopa Andrew, Spreen William R, van Wyk Jean, Cutrell Amy G

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

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.

Для цитирования: Orkin Chloe, Schapiro Jonathan M, Perno Carlo F, Kuritzkes Daniel R, Patel Parul, DeMoor Rebecca, Dorey David, Wang Yongwei, Han Kelong, Van Eygen Veerle, Crauwels Herta, Ford Susan L, Latham Christine L, St Clair Marty, Polli Joseph W, Vanveggel Simon, Vandermeulen Kati, D'Amico Ronald, Garges Harmony P, Zolopa Andrew, Spreen William R, van Wyk Jean, Cutrell Amy G. 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.. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America. 2023. DOI: 10.1093/cid/ciad370.

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