Unconventional use of injectable long-acting cabotegravir and rilpivirine against HIV-1 in PWH in clinical need: 52 weeks real-world data

Abstract Background Long-acting Cabotegravir and Rilpivirine (LA CAB + RPV) shows potential advantages in heavily comorbid and even in viremic people with HIV (PWH). We assessed LA CAB + RPV durability in a cohort of PWH with a high comorbidity burden and adherence issues. Methods Retrospective obse...

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Main Authors: Valentina Iannone, Roberto Rossotti, Nicholas Brian Bana, Gabriele Cavazza, Federico D’Amico, Francesca Lombardi, Pierluigi Francesco Salvo, Gianmaria Baldin, Simona Di Giambenedetto, Dario Bernacchia, Gabriele Pagani, Alberto Borghetti, Stefano Rusconi
Format: Article
Language:English
Published: BMC 2025-01-01
Series:BMC Infectious Diseases
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Online Access:https://doi.org/10.1186/s12879-025-10499-0
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author Valentina Iannone
Roberto Rossotti
Nicholas Brian Bana
Gabriele Cavazza
Federico D’Amico
Francesca Lombardi
Pierluigi Francesco Salvo
Gianmaria Baldin
Simona Di Giambenedetto
Dario Bernacchia
Gabriele Pagani
Alberto Borghetti
Stefano Rusconi
author_facet Valentina Iannone
Roberto Rossotti
Nicholas Brian Bana
Gabriele Cavazza
Federico D’Amico
Francesca Lombardi
Pierluigi Francesco Salvo
Gianmaria Baldin
Simona Di Giambenedetto
Dario Bernacchia
Gabriele Pagani
Alberto Borghetti
Stefano Rusconi
author_sort Valentina Iannone
collection DOAJ
description Abstract Background Long-acting Cabotegravir and Rilpivirine (LA CAB + RPV) shows potential advantages in heavily comorbid and even in viremic people with HIV (PWH). We assessed LA CAB + RPV durability in a cohort of PWH with a high comorbidity burden and adherence issues. Methods Retrospective observational study in two Italian outpatient settings enrolling PWH who switched to LA CAB + RPV from February 2021 to January 2024 in presence of exclusion criteria enlisted in registrational trials or with other worrisome clinical risks. Kaplan-Meier (KM) was used to assess the probability of CAB/RPV discontinuation. Cox regression analysis was used to evaluate potential predictors of discontinuation. Results We enrolled 74 PWH, with a median of 7 injections (IQR 5–9), a median age of 53 years (IQR 45–61), median time of exposure to antiretrovirals of 11 years (IQR 8–18) and median time from HIV diagnosis of 11.8 years (IQR 6.6–18.2). Eleven (14.9%) discontinued LA CAB + RPV mainly for injection-site pain. Of 53 PWH who were undetectable before switch, 37 maintained viral suppression at week 52. We registered only one virological failure at week 12. Twenty-one started injections with unsuppressed viral loads (median 66 cps/ml, IQR 40–215) and 10 (47.6%) achieved viral suppression. Overall probability of discontinuation was 14.9% at week 52. Younger age was protective against discontinuation (HR 0.93, 95%CI 0.88–0.99, p = 0.048). Conclusions Our results support the potential advantages in using LA CAB + RPV in PWH with adherence issues and comorbidities.
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spelling doaj-art-0c6d3b8f6b644c65bea059df22fa338e2025-01-26T12:17:07ZengBMCBMC Infectious Diseases1471-23342025-01-012511710.1186/s12879-025-10499-0Unconventional use of injectable long-acting cabotegravir and rilpivirine against HIV-1 in PWH in clinical need: 52 weeks real-world dataValentina Iannone0Roberto Rossotti1Nicholas Brian Bana2Gabriele Cavazza3Federico D’Amico4Francesca Lombardi5Pierluigi Francesco Salvo6Gianmaria Baldin7Simona Di Giambenedetto8Dario Bernacchia9Gabriele Pagani10Alberto Borghetti11Stefano Rusconi12Department of Healtcare Surveillance and Bioetichs, Section of Infectious Diseases, Catholic University of Sacred HeartDepartment of Infectious Diseases, ASST Grande Ospedale Metropolitano NiguardaDepartment of Infectious Diseases, ASST Grande Ospedale Metropolitano NiguardaDepartment of Infectious Diseases, ASST Grande Ospedale Metropolitano NiguardaDepartment of Infectious Diseases, ASST Grande Ospedale Metropolitano NiguardaDepartment of Healtcare Surveillance and Bioetichs, Section of Infectious Diseases, Catholic University of Sacred HeartDepartment of Healtcare Surveillance and Bioetichs, Section of Infectious Diseases, Catholic University of Sacred HeartDepartment of Medical and Surgical Science, Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Infectious DiseasesDepartment of Healtcare Surveillance and Bioetichs, Section of Infectious Diseases, Catholic University of Sacred HeartClinical and Biomedical Science Department (DIBIC), Infectious Diseases Unit, University of Milan, Legnano General Hospital, ASST Ovest MilaneseClinical and Biomedical Science Department (DIBIC), Infectious Diseases Unit, University of Milan, Legnano General Hospital, ASST Ovest MilaneseDepartment of Clinical and Experimental Medicine, University of PisaClinical and Biomedical Science Department (DIBIC), Infectious Diseases Unit, University of Milan, Legnano General Hospital, ASST Ovest MilaneseAbstract Background Long-acting Cabotegravir and Rilpivirine (LA CAB + RPV) shows potential advantages in heavily comorbid and even in viremic people with HIV (PWH). We assessed LA CAB + RPV durability in a cohort of PWH with a high comorbidity burden and adherence issues. Methods Retrospective observational study in two Italian outpatient settings enrolling PWH who switched to LA CAB + RPV from February 2021 to January 2024 in presence of exclusion criteria enlisted in registrational trials or with other worrisome clinical risks. Kaplan-Meier (KM) was used to assess the probability of CAB/RPV discontinuation. Cox regression analysis was used to evaluate potential predictors of discontinuation. Results We enrolled 74 PWH, with a median of 7 injections (IQR 5–9), a median age of 53 years (IQR 45–61), median time of exposure to antiretrovirals of 11 years (IQR 8–18) and median time from HIV diagnosis of 11.8 years (IQR 6.6–18.2). Eleven (14.9%) discontinued LA CAB + RPV mainly for injection-site pain. Of 53 PWH who were undetectable before switch, 37 maintained viral suppression at week 52. We registered only one virological failure at week 12. Twenty-one started injections with unsuppressed viral loads (median 66 cps/ml, IQR 40–215) and 10 (47.6%) achieved viral suppression. Overall probability of discontinuation was 14.9% at week 52. Younger age was protective against discontinuation (HR 0.93, 95%CI 0.88–0.99, p = 0.048). Conclusions Our results support the potential advantages in using LA CAB + RPV in PWH with adherence issues and comorbidities.https://doi.org/10.1186/s12879-025-10499-0Long acting antiretroviralsPopulation in needComorbiditiesAdherence issuesVirological suppression
spellingShingle Valentina Iannone
Roberto Rossotti
Nicholas Brian Bana
Gabriele Cavazza
Federico D’Amico
Francesca Lombardi
Pierluigi Francesco Salvo
Gianmaria Baldin
Simona Di Giambenedetto
Dario Bernacchia
Gabriele Pagani
Alberto Borghetti
Stefano Rusconi
Unconventional use of injectable long-acting cabotegravir and rilpivirine against HIV-1 in PWH in clinical need: 52 weeks real-world data
BMC Infectious Diseases
Long acting antiretrovirals
Population in need
Comorbidities
Adherence issues
Virological suppression
title Unconventional use of injectable long-acting cabotegravir and rilpivirine against HIV-1 in PWH in clinical need: 52 weeks real-world data
title_full Unconventional use of injectable long-acting cabotegravir and rilpivirine against HIV-1 in PWH in clinical need: 52 weeks real-world data
title_fullStr Unconventional use of injectable long-acting cabotegravir and rilpivirine against HIV-1 in PWH in clinical need: 52 weeks real-world data
title_full_unstemmed Unconventional use of injectable long-acting cabotegravir and rilpivirine against HIV-1 in PWH in clinical need: 52 weeks real-world data
title_short Unconventional use of injectable long-acting cabotegravir and rilpivirine against HIV-1 in PWH in clinical need: 52 weeks real-world data
title_sort unconventional use of injectable long acting cabotegravir and rilpivirine against hiv 1 in pwh in clinical need 52 weeks real world data
topic Long acting antiretrovirals
Population in need
Comorbidities
Adherence issues
Virological suppression
url https://doi.org/10.1186/s12879-025-10499-0
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