Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2024 Dec 1;97(4):e1-e5.
doi: 10.1097/QAI.0000000000003501.

Brief Report: Switching to Long-Acting CAB/RPV: Data From an Italian Monocentric Cohort

Affiliations
Observational Study

Brief Report: Switching to Long-Acting CAB/RPV: Data From an Italian Monocentric Cohort

Maddalena Matone et al. J Acquir Immune Defic Syndr. .

Abstract

Background: Cabotegravir (CAB)/rilpivirine (RPV) is the first long-acting injectable (LAI) antiretroviral therapy approved for virologically suppressed adults with HIV-1.

Setting: Italian single centre cohort.

Methods: We conducted a retrospective observational study to assess the durability, adherence to the prescribed injection schedule, and reasons for discontinuation of CAB/RPV LAI administered every 8 weeks (Q8W).

Results: One hundred thirty-eight patients were included with a median observation period of 43 weeks [interquartile range (IQR) 34-47 weeks]. Of these, 32 (23.2%) were female, and the median age was 51 years (IQR 40-58 years). Twelve patients (8.7%) discontinued CAB/RPV LAI treatment with a median time to discontinuation of 21 weeks (IQR 12-35 weeks), and 92.8% of the injections occurred within the CAB/RPV LAI schedule. The most common reason for discontinuation was injection-related pain (5/12). No confirmed virological failure occurred during the period of observation with 3 individuals who experienced virological blips.

Conclusions: Our findings showed that CAB/RPV LAI Q8W is tolerated well in clinical practice, with high adherence to the injection schedule and few discontinuations mainly related to injection site-related pain.

Keywords: HIV; adherence; cabotegravir; discontinuation; long-acting antiretroviral therapy; rilpivirine.

PubMed Disclaimer

Conflict of interest statement

The authors have no funding or conflicts of interest to disclose. All authors have reviewed and approved the final version of this manuscript and affirm that this work is free from any potential conflicts of interest.

Figures

FIGURE 1.
FIGURE 1.
The Kaplan–Meier curve depicts the probability of treatment continuation over time up to 48 weeks. Vertical dashes indicate censored data (end of observation while on therapy).
FIGURE 2.
FIGURE 2.
Distribution of injection delays beyond the ±7-day window.

Similar articles

References

    1. Altice F, Evuarherhe O, Shina S, et al. Adherence to HIV treatment regimens: systematic literature review and meta-analysis. Patient Prefer Adherence. 2019;13:475–490. - PMC - PubMed
    1. Nachega JB, Scarsi KK, Gandhi M, et al. Long-acting antiretrovirals and HIV treatment adherence. Lancet HIV. 2023;10:e332–e342. - PMC - PubMed
    1. FDA Approves Cabenuva and Vocabria for the Treatment of HIV-1 Infection. FDA. Available at: https://www.fda.gov/drugs/human-immunodeficiency-virus-hiv/fda-approves-.... Accessed January 8, 2024.
    1. Margolis DA, Gonzalez-Garcia J, Stellbrink HJ, et al. Long-acting intramuscular cabotegravir and rilpivirine in adults with HIV-1 infection (LATTE-2): 96-week results of a randomised, open-label, phase 2b, non-inferiority trial. Lancet. 2017;390:1499–1510. - PubMed
    1. Rizzardini G, Overton ET, Orkin C, et al. Long-acting injectable cabotegravir + rilpivirine for HIV maintenance therapy: week 48 pooled analysis of phase 3 ATLAS and FLAIR trials. J Acquir Immune Defic Syndr. 2020;85:498–506. - PMC - PubMed

Publication types