P-383. Reasons for discontinuation of CAB+RPV LA for HIV treatment in the OPERA Cohort: A CHORUS survey of healthcare providers
Ricky K Hsu, Michael D Osterman, Jennifer S Fusco, Rachel Palmieri Weber, Michael G Sension, Michael B Wohlfeiler, Quateka Cochran, Gayathri Sridhar, Vani Vannappagari, Kimberley Brown, Jean A van Wyk, Gregory P Fusco

TL;DR
This study explores why healthcare providers report discontinuation of CAB+RPV LA, a long-acting HIV treatment, in real-world clinical settings.
Contribution
The study provides real-world insights into discontinuation reasons for CAB+RPV LA, a long-acting HIV treatment, based on healthcare provider reports.
Findings
Loss to follow-up and non-adherence were the most common reasons for discontinuation.
Only a small percentage of discontinuations were due to injection site reactions or adverse events.
One-third of patients intended to restart CAB+RPV LA injections.
Abstract
Recent drug development has focused on long-acting (LA) formulations of antiretrovirals for the treatment of HIV. Cabotegravir + rilpivirine LA (CAB+RPV LA) is the only complete LA antiretroviral therapy (ART) regimen approved for the treatment of HIV-1 in the US with injections every month or every two months. Despite its increasing use, reasons for discontinuation of injections have not been routinely investigated. This study aims to describe reasons for discontinuation of CAB+RPV LA in routine clinical care. Healthcare providers (HCPs) that used the CHORUS mobile application between 27JUN2024 and 21JAN2025 were eligible for participation. HCPs were invited to complete a two-question survey for each individual in their care who had either (a) ≥ 61 days since their first CAB+RPV LA injection without another injection or (b) ≥ 61 or ≥ 91 days without an injection after initiating…
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Taxonomy
TopicsHIV/AIDS drug development and treatment · HIV/AIDS Research and Interventions · Pharmaceutical Quality and Counterfeiting
