Effectiveness and risk factors for virological outcome of darunavir-based therapy for treatment-experienced HIV-infected patients

Abstract

Objective: We evaluated the effectiveness of darunavir (DRV) treatment plus an optimized background regimen in 120 HIV-1 treatment-experienced patients. Design: Retrospective cohort, multicenter study. Methods: Adults >16years with virological treatment failure starting therapy with a DRV-containing regimen were included. Effectiveness was evaluated as the percentage of patients with an undetectable HIV-1 RNA viral load (<50 and <200copies/mL) after 48weeks, and changes in CD4+ cell counts. We evaluated the risk factors associated with treatment failure. Results: Of the cohort, 83% were men with a median age of 45years (interquartile range, IQR 40-51). They had experienced treatment for a median of 13years (IQR 9-17) with a median of six previous regimens (IQR 4-7), all using protease inhibitors. After treatment, 82% (95% confidence interval, CI 74-88%) of patients had an HIV-1 RNA viral load <200copies/mL and 69% (95% CI 60-76%) had <50copies/mL. The CD4+ cell count increased by 378cells/μL (IQR 252-559; P<0.001 vs. baseline). Risk factors associated with poor outcome were age >40years [odds ratio, OR 0.15 (95% CI 0.10-0.78); P=0.015], use of raltegravir in the regimen [OR 0.37 (95% CI 0.10-0.97); P=0.046], and baseline CD4+ cell count <200cells/μL [OR 2.79 (95% CI 1.11-6.97); P=0.028]. Conclusion: In this Mexican cohort Darunavir was metabolically safe, well tolerated and achieved high rates of virological suppression in highly treatment-experienced patients infected with HIV-1.