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      Sustained Virological Response on Second-Line Antiretroviral Therapy following Virological Failure in HIV-Infected Patients in Rural South Africa

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          Abstract

          Objective

          This study aims to describe the virological, immunological and clinical efficacy of protease inhibitor (PI)-based second-line antiretroviral therapy (ART) in rural South Africa.

          Methods

          An observational cohort study was performed on 210 patients (including 39 children) who initiated PI-based second-line therapy at least 12 months prior to data collection. Biannual clinical, immunological and virological monitoring was performed. Primary endpoints were adequate virological response (plasma HIV-1 RNA<400 copies/ml), full virological suppression (plasma HIV-1 RNA<50 copies/ml) and treatment failure (virological failure (plasma HIV-1 RNA>1000 after initial virological response) or on-going viremia (plasma HIV-1 RNA never<400 copies/ml for more than six months)). Data were analyzed by an on-treatment (OT) and intention-to-treat (ITT) approach. Analyses were primarily performed on the group of patients who switched following first-line virological failure.

          Results

          Median duration of follow-up after switch to second-line treatment was 20 months [IQR 11–35]. 191 patients had switched to second-line ART due to first-line virological failure. 139/191 of them (72.8%, ITT) were in care and on treatment at the end of follow-up and 11/191 (5.8%, ITT) had died. After twelve months, an adequate virological response was seen in 92/128 patients (71.9%, OT), of which 78/128 (60.9%, OT) experienced full virological suppression. Virological response remained stable after 24 months. Virological efficacy was similar amongst adult and pediatric patients. As in first-line ART, we observed a lack of correlation between virological failure and WHO-defined immunological failure.

          Conclusions

          Good virological outcomes following first-line failure can be achieved with PI-based, second-line antiretroviral therapy in both adult and pediatric patients in rural South Africa. Retention rates were high and virological outcomes were sustainable during the two-year follow-up period, although persisting low-level viremia occurred in a subset of patients. The observed viro-immunological dissociation emphasizes the need for virological monitoring.

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          Author and article information

          Contributors
          Role: Editor
          Journal
          PLoS One
          PLoS ONE
          plos
          plosone
          PLoS ONE
          Public Library of Science (San Francisco, USA )
          1932-6203
          2013
          11 March 2013
          : 8
          : 3
          : e58526
          Affiliations
          [1 ]Department of Internal Medicine and Infectious Diseases, University Medical Centre Utrecht, Utrecht, The Netherlands
          [2 ]Department of Virology, University Medical Centre Utrecht, Utrecht, The Netherlands
          [3 ]Ndlovu Care Group, Elandsdoorn, Limpopo, South Africa
          [4 ]Department of Paediatric Infectious Diseases, University Medical Centre Utrecht, Utrecht, The Netherlands
          University of Pittsburgh, United States of America
          Author notes

          Competing Interests: None of the authors have a financial interest in or a financial conflict with the subject matter and materials discussed in this manuscript. A.F.S. has received financial support for travel, accommodation and meeting expenses from ViiV healthcare. A.M.J.W. has received financial support for research, travel, speaking engagement or consultancy from BMS, Gilead, Janssen, MSD, ViiV healthcare and Virology Education and grant support from MSD, Pfizer and ViiV healthcare. H.A.T. has received financial support for employment from Royal Netherlands Embassy (RNE) and grant support from USAID. S.P.M.G. has received financial support for employment from PharmAccess Foundation. A.I.M.H. is member of the advisory board of BMS, Gilead, ViiV healthcare, Janssen and MSD and has received financial grant support from Gilead, Janssen, MSD and Roche. R.E.B. has received no financial support. This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials.

          Contributed to the writing of the manuscript: HAT AIMH. Conceived and designed the experiments: AFS AMJW SPMG AIMH REB. Performed the experiments: AFS HAT REB. Analyzed the data: AFS REB. Wrote the paper: AFS AMJW HAT SPMG AIMH REB.

          Article
          PONE-D-12-35938
          10.1371/journal.pone.0058526
          3594302
          23505529
          a7c251da-a6c0-404f-b313-6b0a850475e5
          Copyright @ 2013

          This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

          History
          : 6 November 2012
          : 5 February 2013
          Page count
          Pages: 8
          Funding
          The authors have no support or funding to report.
          Categories
          Research Article
          Medicine
          Clinical Research Design
          Cohort Studies
          Longitudinal Studies
          Observational Studies
          Epidemiology
          Pharmacoepidemiology
          Global Health
          Infectious Diseases
          Viral Diseases
          HIV
          HIV clinical manifestations
          HIV diagnosis and management
          HIV epidemiology

          Uncategorized
          Uncategorized

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