Objectives: The efficacy and safety of lopinavir/ritonavir monotherapy has been explored with promising results in well-controlled, randomized clinical trials. However, less information about its clinical usefulness in routine clinical practice is currently available. The objective of this study was to assess the effectiveness and safety of monotherapy with lopinavir/ritonavir as a treatment simplification strategy in HIV-infected patients with viral suppression outside a clinical trial setting. Methods: Fifty-one subjects who were switched to lopinavir/ritonavir monotherapy and whose HIV-1 RNA was < 50 copies/mL were included in this retrospective study. Data were obtained from a prospectively compiled database. The primary endpoint was the percentage of subjects who maintained viral suppression after 48 weeks of follow-up. Secondary endpoints included the incidence of adverse events and changes in CD4+ T cell count and in lipid profile. Results: Two patients lost viral suppression, seven patients interrupted lopinavir/ritonavir monotherapy because of adverse events and four patients were lost before completing 48 weeks of follow-up. Thus, 38/40 (95.0%) patients maintained viral suppression when only subjects whose outcomes were available up to week 48 were considered and 38/51 (74.5%) patients maintained viral suppression when subjects who discontinued therapy or who were lost to follow-up were considered as treatment failures. The mean CD4+ T cell count significantly increased, from 541 (280) cells/mm 3 at baseline to 609 (212) cells/mm 3 at week 48 of follow-up (P = 0.034). This increase was similar to that observed in the 48 weeks prior to lopinavir/ritonavir monotherapy (P = 0.792). Although total cholesterol remained unchanged, there was a significant decrease in triglyceride levels during follow-up (P = 0.029). Conclusions: Monotherapy with lopinavir/ritonavir is safe and effective as a treatment simplification approach in HIV-1-infected patients with sustained viral suppression in routine clinical practice, particularly in those patients already receiving a lopinavir/ritonavir-based antiretroviral regimen. © The Author 2007.
|Journal||Journal of Antimicrobial Chemotherapy|
|Publication status||Published - 1 Aug 2007|
- HIV infection
- Nucleoside-sparing therapy
- Protease inhibitors