Abstract

IntroductionAssessing virological response of four-drugs antiretroviral regimen that include raltegravir (RAL) in naïve patients with high viral load (>500,000 copies/mL) selected from a multicentre Italian database.MethodsNaïve patients with HIV RNA>500,000 copies/mL, who began standard antiretroviral regimens either based on non-nucleoside reverse transcriptase inhibitors (NNRTI) or boosted-PI (PI/r), or a standard regimen plus RAL between 2008 and 2013 were analyzed. Observation was censored at 12 months and the percentage of patients who achieved a viral load below the limit of detection (BLD) was calculated. Virological failure was defined as two consecutive viral loads>40 copies/mL.ResultsOverall, 179 patients were included (13% with primary HIV infection (PHI), and 42.5% with AIDS diagnosis). Of them, 156 started standard three-drugs antiretroviral regimen (75.6% PI/r-based, 24.4% NNRTI-based. Among patients with PHI, 23 patients (12.8%), 6 (25%) started a four-drugs antiretroviral regimen containing both RAL and PI/r. Patients’ characteristics were as follows: males 74%, median age 42 years (IQR 35–51), sexually transmission 75.1%, median CD4 count 156 cells/µL (IQR 47–368) and median HIV-RNA 6.1 log10 copies/mL (IQR 5.8–6.4). 91 of 179 patients (50.8%) reached BLD viral load during the twelve months of observation. Three patients (1.7%) who began regimens PI/r-based with three-drugs had virological rebound after reaching BLD viral load. By use of survival analysis, we show that those patients who added RAL to the standard regimen have reached the primary end point faster (mean 8.4 months (95% CI 7.2–9.6) vs 11.4 (95% CI 11.0–11.8) in PI group and 10.3 (95% CI 9.4–11.1) in NNRTI group; p<0.001, Figure 1). In the adjusted analysis, the choice of a standard regimen versus a four-drugs regimen was driven only by higher baseline viral load (OR. 9.05; 95% CI 2.41–37.41; p=0.001).ConclusionsOnly half of the naïve patients who began antiretroviral therapy having >500,000 copies/mL HIV-RNA had virological success at 12 months. The success was reached faster using the RAL-containing four-drugs regimen, suggesting that strengthening the initial regimen could be an option in patients with very high viral load to improve virological response.

Highlights

  • Assessing virological response of four-drugs antiretroviral regimen that include raltegravir (RAL) in naıve patients with high viral load ( 500,000 copies/mL) selected from a multicentre Italian database

  • Four-drugs regimen containing raltegravir is highly effective in HIV patients starting therapy with 500,000 copies/mL viral load

  • Observation was censored at 12 months and the percentage of patients who achieved a viral load below the limit of detection (BLD) was calculated

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Introduction

Assessing virological response of four-drugs antiretroviral regimen that include raltegravir (RAL) in naıve patients with high viral load ( 500,000 copies/mL) selected from a multicentre Italian database. Four-drugs regimen containing raltegravir is highly effective in HIV patients starting therapy with 500,000 copies/mL viral load Introduction: Assessing virological response of four-drugs antiretroviral regimen that include raltegravir (RAL) in naıve patients with high viral load ( 500,000 copies/mL) selected from a multicentre Italian database.

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