# Antiretroviral Treatment Switch Among Treatment-Experienced People with HIV

**Authors:** Benjamin Chastek, Uche Mordi, Mary J. Christoph, Lisa B. Le, Travis Lim, Sunil Majethia, Cassidy Trom, Joshua Cohen

PMC · DOI: 10.36469/001c.156180 · Journal of Health Economics and Outcomes Research · 2026-02-24

## TL;DR

This study shows that people with HIV who take B/F/TAF are less likely to switch their treatment compared to other regimens.

## Contribution

The study identifies B/F/TAF as a regimen associated with lower treatment switching in treatment-experienced HIV patients.

## Key findings

- PWH taking B/F/TAF had a significantly lower risk of treatment switch/add-on compared to other regimens.
- The findings were consistent in both the overall population and Medicare Advantage enrollees.
- B/F/TAF users maintained their regimen longer than those on other ART regimens.

## Abstract

HIV requires lifelong continuous antiretroviral therapy (ART) to prevent morbidity and mortality and to reduce onward transmission. People with HIV (PWH) may switch ART regimens for various clinical and nonclinical reasons. Identifying patterns of ART switching can inform shared decision-making and optimize regimen selection among treatment-experienced PWH.

To describe and compare treatment switching among PWH by regimen in a large US claims database, including a subset of PWH enrolled in Medicare Advantage.

A retrospective analysis of closed US medical and pharmacy claims data was conducted in treatment-experienced PWH with commercial insurance or Medicare Advantage with Part D coverage from the Optum Research Database. PWH who switched to an ART regimen of interest (bictegravir/emtricitabine/tenofovir alafenamide [B/F/TAF], dolutegravir/lamivudine, dolutegravir/abacavir/lamivudine, dolutegravir + emtricitabine/tenofovir alafenamide, dolutegravir + emtricitabine/tenofovir disoproxil fumarate, and cabotegravir + rilpivirine) between July 1, 2017, and November 30, 2023, were included. Baseline characteristics were balanced across regimens in the overall study population using inverse probability treatment weighting. Time to switch/add-on was estimated using Kaplan-Meier analyses. Adjusted hazard ratios for the entire follow-up period were calculated using multivariable Cox proportional hazards models. Outcomes were assessed in the overall population and in the subset enrolled in Medicare Advantage.

Overall, 14 826 treatment-experienced PWH were included in the study. The proportion of PWH without switch/add-on after the first 12 months of follow-up was greater for those who were taking B/F/TAF compared with those taking the other regimens of interest (all P < .001). The risk of switch/add-on was significantly lower for those who were taking B/F/TAF vs those taking the other regimens of interest (all P ≤ .001). Findings were similar for the subset of Medicare Advantage enrollees.

Due to more effective treatments, PWH have increased life expectancy, and a growing proportion are qualifying for Medicare coverage. This analysis showed that PWH taking B/F/TAF, both in the overall population and the Medicare Advantage subset, maintained their initial treatment regimen longer and had a reduced risk of treatment switch/add-on compared with the other regimens of interest.

These findings suggest that B/F/TAF has a lower likelihood of treatment switch/add-on for treatment-experienced PWH than other current ART regimens.

## Linked entities

- **Chemicals:** bictegravir/emtricitabine/tenofovir alafenamide (PubChem CID 129626368)

## Full-text entities

- **Diseases:** PWH (MESH:C000719191), HIV (MESH:D015658), nervous system disorders (MESH:D009422), intervertebral disc disorders (MESH:C535531), back problems (MESH:D019567), AIDS (MESH:D000163), anxiety disorders (MESH:D001008), Comorbidity (MESH:D004194), spondylosis (MESH:D055009)
- **Chemicals:** CAB (MESH:C584914), steroids (MESH:D013256), cobicistat (MESH:D000069547), ABC (-), abacavir (MESH:C106538), emtricitabine/tenofovir alafenamide (MESH:C000613801), F (MESH:D005461), DTG (MESH:C562325), 3TC (MESH:D019259), RPV (MESH:D000068696), B (MESH:D001895), tenofovir disoproxil fumarate (MESH:D000068698), TAF (MESH:C442442), elvitegravir (MESH:C509700), bictegravir (MESH:C000620396)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940528/full.md

## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC12940528/full.md

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Source: https://tomesphere.com/paper/PMC12940528