Published in:
Open Access
01-10-2020 | Human Immunodeficiency Virus | Original Paper
Treatment modification after starting cART in people living with HIV: retrospective analysis of the German ClinSurv HIV Cohort 2005–2017
Authors:
Melanie Stecher, Philipp Schommers, Christian Kollan, Matthias Stoll, Frieder Kuhlendahl, Hans-Jürgen Stellbrink, Jan-Christian Wasmuth, Christoph Stephan, Laura Hamacher, Clara Lehmann, Christoph Boesecke, Johannes Bogner, Stefan Esser, Carlos Fritzsche, Annette Haberl, Dirk Schürmann, Olaf Degen, Heinz-August Horst, Christian Hoffmann, Björn Jensen, Carolynne Schwarze-Zander, Martin Platten, Gerd Fätkenheuer, Daniel Schmidt, Barbara Gunsenheimer-Bartmeyer, Jörg Janne Vehreschild, On behalf of the ClinSurv Study Group
Published in:
Infection
|
Issue 5/2020
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Abstract
Objective
Combination antiretroviral therapy (cART) has markedly increased survival and quality of life in people living with HIV. With the advent of new treatment options, including single-tablet regimens, durability and efficacy of first-line cART regimens are evolving.
Methods
We analyzed data from the prospective multicenter German Clinical Surveillance of HIV Disease (ClinSurv) cohort of the Robert-Koch Institute. Kaplan–Meier and Cox proportional hazards models were run to examine the factors associated with treatment modification. Recovery after treatment initiation was analyzed comparing pre-cART viral load and CD4+ T-cell counts with follow-up data.
Results
We included 8788 patients who initiated cART between 2005 and 2017. The sample population was predominantly male (n = 7040; 80.1%), of whom 4470 (63.5%) were reporting sex with men as the transmission risk factor. Overall, 4210 (47.9%) patients modified their first-line cART after a median time of 63 months (IQR 59–66). Regimens containing integrase strand transfer inhibitors (INSTI) were associated with significantly lower rates of treatment modification (adjusted hazard ratio 0.44; 95% CI 0.39–0.50) compared to protease inhibitor (PI)-based regimens. We found a decreased durability of first-line cART significantly associated with being female, a low CD4+ T-cell count, cART initiation in the later period (2011–2017), being on a multi-tablet regimen (MTR).
Conclusions
Drug class and MTRs are significantly associated with treatment modification. INSTI-based regimens showed to be superior compared to PI-based regimens in terms of durability.