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Regimen Selection in the OPTIONS Trial of HIV Salvage Therapy: Drug Resistance, Prior Therapy, and Race-ethnicity Determine the Degree of Regimen Complexity

Overview
Journal HIV Clin Trials
Date 2015 Jul 28
PMID 26212575
Citations 4
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Abstract

Background: Regimen selection for highly treatment-experienced patients is complicated.

Methods: Using a web-based utility, study team members reviewed antiretroviral (ARV) history and resistance data and recommended individual ARV regimens and nucleoside reverse transcriptase inhibitor (NRTI) options for treatment-experienced participants consisting of 3-4 of the following agents: raltegravir (RAL), darunavir (DRV)/ritonavir, tipranavir (TPV)/ritonavir, etravirine (ETR), maraviroc (MVC), and enfuvirtide (ENF). We evaluated team recommendations and site selection of regimen and NRTIs. Associations between baseline factors and the selection of a complex regimen (defined as including four ARV agents or ENF) were explored with logistic regression.

Results: A total of 413 participants entered the study. Participants initiated the first or second recommended regimen 86% of the time and 21% of participants started a complex regimen. In a multivariable model, ARV resistance to NRTI (odds ratio [OR] = 2.2), non-nucleoside reverse transcriptase inhibitor (NNRTI, OR = 6.2) or boosted protease inhibitor (PI, OR = 6.6), prior use of integrase strand transfer inhibitor (INSTI, OR = 25), and race-ethnicity (all P ≤ 0.01) were associated with selection of a complex regimen. Black non-Hispanic (OR = 0.5) and Hispanic participants from the continental US (OR = 0.2) were less likely to start a complex regimen, compared to white non-Hispanics.

Conclusions: In this multi-center trial, we developed a web-based utility that facilitated treatment recommendations for highly treatment-experienced patients. Drug resistance, prior INSTI use, and race-ethnicity were key factors in decisions to select a more complex regimen.

Citing Articles

Long-term Outcomes in a Large Randomized Trial of HIV-1 Salvage Therapy: 96-Week Results of AIDS Clinical Trials Group A5241 (OPTIONS).

Gandhi R, Tashima K, Smeaton L, Vu V, Ritz J, Andrade A J Infect Dis. 2019; 221(9):1407-1415.

PMID: 31135883 PMC: 7137888. DOI: 10.1093/infdis/jiz281.


Training Internal Medicine Residents to Provide Care and Treatment for Human Immunodeficiency Virus-1-Infected Patients.

Valenti S, Johnson L, Szpunar S, Hilu R, Saravolatz L Open Forum Infect Dis. 2019; 6(4):ofz093.

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A dual regimen of ritonavir/darunavir plus dolutegravir for rescue or simplification of rescue therapy: 48 weeks' observational data.

Capetti A, Cossu M, Orofino G, Sterrantino G, Cenderello G, De Socio G BMC Infect Dis. 2017; 17(1):658.

PMID: 28964268 PMC: 5622573. DOI: 10.1186/s12879-017-2755-4.


HIV Salvage Therapy Does Not Require Nucleoside Reverse Transcriptase Inhibitors: A Randomized, Controlled Trial.

Tashima K, Smeaton L, Fichtenbaum C, Andrade A, Eron J, Gandhi R Ann Intern Med. 2015; 163(12):908-17.

PMID: 26595748 PMC: 4681296. DOI: 10.7326/M15-0949.

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