# Efficacy of Long-Acting Injectable Cabotegravir and Rilpivirine Compared With Daily Oral Antiretroviral Therapy in Patients With HIV: A Systematic Review

**Authors:** Jesus Endara-Mina, Mayuri Quishpe, Emely Vera, Nicolás Haro, Alisson Guzmán, Jefferson Guillin, Kleber Quisnancela, Henry Sarmiento-Vallejo, Isabel Mantilla-Alcivar, Carlos Cabrera, Jairo Cueva, Shirley Serrano, Catherine Caiza, Cesar Intriago, Paulina Salazar

PMC · DOI: 10.7759/cureus.103429 · Cureus · 2026-02-11

## TL;DR

Injectable HIV treatment every 4-8 weeks is as effective as daily pills and improves patient satisfaction and adherence.

## Contribution

Demonstrates the non-inferiority and improved adherence of long-acting injectable HIV therapy compared to daily oral regimens.

## Key findings

- CAB/RPV-LA achieved durable virological suppression exceeding 90% over 48-240 weeks.
- Injectable regimen showed higher treatment satisfaction and excellent adherence within dosing windows.
- Adverse events were mainly mild injection-site reactions with less than 1% discontinuation.

## Abstract

Long-acting antiretroviral therapy (ART) has emerged as an innovative strategy to address limitations associated with daily oral regimens in people living with human immunodeficiency virus type 1 (HIV-1), including adherence barriers, treatment fatigue, and social stigma. This systematic review, conducted in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 guidelines and registered in International Prospective Register of Systematic Reviews (PROSPERO, CRD420251155009), identified randomized clinical trials comparing long-acting injectable cabotegravir and rilpivirine (CAB/RPV-LA) with standard daily oral ART through searches of PubMed, ScienceDirect, the Cochrane Library, and Google Scholar. Ten randomized trials involving 5,619 adults with HIV-1 were included. CAB/RPV-LA, administered intramuscularly every four or eight weeks, achieved durable virological suppression exceeding 90% across follow-up periods of 48 to 240 weeks, demonstrating non-inferiority to daily oral ART. Patient-reported outcomes consistently favored the injectable regimen, with higher treatment satisfaction scores and excellent adherence within the dosing window, while adverse events were mainly mild-to-moderate injection-site reactions (ISRs), resulting in treatment discontinuation in fewer than 1% of participants. Overall, the certainty of evidence was high for virological efficacy and moderate for safety and satisfaction outcomes, supporting long-acting CAB/RPV-LA as an effective and well-tolerated alternative that improves adherence, convenience, and quality of life in long-term HIV management.

## Linked entities

- **Chemicals:** cabotegravir (PubChem CID 54713659), rilpivirine (PubChem CID 6451164)

## Full-text entities

- **Diseases:** HIV (MESH:D015658), fatigue (MESH:D005221)
- **Chemicals:** Cabotegravir (MESH:C584914), RPV-LA (-), Rilpivirine (MESH:D000068696)
- **Species:** Human immunodeficiency virus 1 (no rank) [taxon 11676], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12987598/full.md

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Source: https://tomesphere.com/paper/PMC12987598