PMID- 23016535 OWN - NLM STAT- MEDLINE DCOM- 20130802 LR - 20211021 IS - 1931-8405 (Electronic) IS - 0889-2229 (Print) IS - 0889-2229 (Linking) VI - 29 IP - 3 DP - 2013 Mar TI - Long-term efficacy and safety of atazanavir/ritonavir treatment in a real-life cohort of treatment-experienced patients with HIV type 1 infection. PG - 564-73 AB - Atazanavir-based regimens have established efficacy and safety in both antiretroviral (ARV)-naive and -experienced patients. However, data evaluating effectiveness beyond 2 years is sparse. Therefore, we assessed the long-term outcomes of ritonavir-boosted atazanavir (ATV/r)-containing regimens in ARV-experienced patients in a clinical setting in a noncomparative, retrospective, observational study collecting data from three European HIV databases on ARV-experienced adults with HIV-1 infection starting an ATV/r-based regimen. Data were extracted every 6 months (maximum follow-up 5 years). Primary outcome was the proportion of patients remaining on ATV/r by baseline HIV-1 RNA (<500 or >/=500 copies/ml). Secondary outcomes included time to virologic failure, reasons for discontinuation, and long-term safety profile. The duration of treatment and time to virologic failure were analyzed using the Kaplan-Meier method. Data were analyzed for 1,294 ARV-experienced patients (male 74%; mean ART exposure 5.7 years). After 3 years, 56% (95% CI: 52%, 60%) of patients with baseline HIV-1 RNA <500 copies/ml and 53% (95% CI: 49%, 58%) of those with HIV-1 RNA >/=500 copies/ml remained on ATV/r. After 3 years, 75% (95% CI: 69%, 80%) of patients with baseline HIV-1 RNA <50 copies/ml remained suppressed and 51% (95% CI: 47%, 55%) of those with baseline HIV-1 RNA >/=50 copies/ml achieved and maintained virologic suppression. Although adverse events (AEs) were the main known reason for discontinuation, no unexpected AEs were observed. In a real-life setting ATV/r-based regimens demonstrated sustained virologic suppression in ARV-experienced patients. After long-term therapy the majority of patients remained on treatment and no unexpected AEs were observed. FAU - Jansen, Klaus AU - Jansen K AD - Competence Network for HIV/AIDS, Ruhr-Universitat, Bochum, Germany. klaus.jansen@klinikum-bochum.de FAU - Sonnerborg, Anders AU - Sonnerborg A FAU - Brockmeyer, Norbert AU - Brockmeyer N FAU - Thalme, Anders AU - Thalme A FAU - Svedhem, Veronica AU - Svedhem V FAU - Dupke, Stephan AU - Dupke S FAU - Eychenne, Jean-Luc AU - Eychenne JL FAU - Nakonz, Tina AU - Nakonz T FAU - Jimenez-Exposito, Maria Jesus AU - Jimenez-Exposito MJ FAU - Pugliese, Pascal AU - Pugliese P LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20121127 PL - United States TA - AIDS Res Hum Retroviruses JT - AIDS research and human retroviruses JID - 8709376 RN - 0 (Anti-HIV Agents) RN - 0 (Oligopeptides) RN - 0 (Pyridines) RN - 0 (RNA, Viral) RN - 4MT4VIE29P (Atazanavir Sulfate) RN - O3J8G9O825 (Ritonavir) SB - IM MH - Adolescent MH - Adult MH - Aged MH - Aged, 80 and over MH - Anti-HIV Agents/*administration & dosage/adverse effects MH - Atazanavir Sulfate MH - Cohort Studies MH - Data Collection/methods MH - Databases, Factual MH - Europe MH - Female MH - HIV Infections/*drug therapy/virology MH - HIV-1/*isolation & purification MH - Humans MH - Male MH - Middle Aged MH - Oligopeptides/*administration & dosage/adverse effects MH - Pyridines/*administration & dosage/adverse effects MH - RNA, Viral/blood MH - Retrospective Studies MH - Ritonavir/*administration & dosage/adverse effects MH - Treatment Outcome MH - Viral Load MH - Young Adult PMC - PMC3698683 EDAT- 2012/09/29 06:00 MHDA- 2013/08/03 06:00 PMCR- 2013/03/01 CRDT- 2012/09/29 06:00 PHST- 2012/09/29 06:00 [entrez] PHST- 2012/09/29 06:00 [pubmed] PHST- 2013/08/03 06:00 [medline] PHST- 2013/03/01 00:00 [pmc-release] AID - 10.1089/aid.2012.0092 [pii] AID - 10.1089/aid.2012.0092 [doi] PST - ppublish SO - AIDS Res Hum Retroviruses. 2013 Mar;29(3):564-73. doi: 10.1089/aid.2012.0092. Epub 2012 Nov 27.