Durability of viral suppression with first-line antiretroviral therapy in patients with HIV in the UK: an observational cohort study

Jemma L. O’Connor(University College London), Colette Smith(University College London), Fiona Lampe(University College London), Margaret Johnson(Royal Free London NHS Foundation Trust), David R. Chadwick(James Cook University Hospital), Mark Nelson(Chelsea and Westminster Hospital), David Dunn(University College London), Alan Winston(St Mary's Hospital), Frank A. Post(King's College Hospital NHS Foundation Trust), Caroline Sabin(University College London), Andrew Phillips(Public Health England), Jonathan Ainsworth, Sris Allan, Jane Anderson, Abdel Babiker, David Chadwick(James Cook University Hospital), Valérie Delpech, David Dunn(University College London), Martin Fisher, Brian Gazzard, Richard Gilson, Mark Gompels(Chelsea and Westminster Hospital), Phillip Hay(University College London), Teresa Hill(University College London), Margaret Johnson(Royal Free London NHS Foundation Trust), Sophie José, Stephen Kegg, Clifford Leen, Fabiola Martin, Mark Nelson(Chelsea and Westminster Hospital), Chloe Orkin, Adrian Palfreeman, Andrew Phillips(Public Health England), Deenan Pillay, Frank A. Post(King's College Hospital NHS Foundation Trust), Jillian Pritchard, Caroline Sabin(University College London), Memory Sachikonye, Achim Schwenk, Anjum Tariq, Roy Trevelion, John Walsh(Royal Free London NHS Foundation Trust), Adam Glabay, Nicky Perry(University College London), Stuart Tilbury, Elaney Youssef, Duncan Churchill, Brian Gazzard, Mark Nelson(Chelsea and Westminster Hospital), Russell J. Everett, David Asboe, Sundhiya Mandalia, Frank A. Post(King's College Hospital NHS Foundation Trust), Hardik Korat, Chris Taylor, Zachary Gleisner, Fowzia Ibrahim(University College London), Linda Campbell, Richard Gilson, Nataliya Brima(University College London), Ian Williams, Margaret Johnson(Royal Free London NHS Foundation Trust), M Youle(Chelsea and Westminster Hospital), Fiona Lampe(University College London), Colette Smith(University College London), Rob Tsintas, Clinton Chaloner, Sharon Hutchinson, Caroline Sabin(University College London), Andrew Phillips(Public Health England), Teresa Hill(University College London), Sophie José, A. Thornton, Susie Huntington, Joan Walsh(Royal Free London NHS Foundation Trust), Nicky Mackie(University College London), Alan Winston(St Mary's Hospital), Jonathan Weber(Royal Free London NHS Foundation Trust), Farhan Ramzan(University College London), Melanie Carder(Chelsea and Westminster Hospital), Chloe Orkin, Janet Lynch(Royal Free London NHS Foundation Trust), James Hand(Royal Free London NHS Foundation Trust), Cintya de Oliveira Souza, Jane Anderson(Royal Free London NHS Foundation Trust), Sajid Munshi, Jonathan Ainsworth(Royal Free London NHS Foundation Trust), Achim Schwenk, Sheila Miller, Christopher Wood, Clifford Leen, Andrew Wilson, Sheila Morris, Mark Gompels(Chelsea and Westminster Hospital), Sophie Allan, Adrian Palfreeman, Khairuddin Memon, Adam Lewszuk, David Chadwick(James Cook University Hospital), Emily K. Cope, James J. Gibson(Royal Free London NHS Foundation Trust), Stephen Kegg, Patricia A. Main(University College London), Sue Mitchell, Matthew F. Hunter(Chelsea and Westminster Hospital), Mandeep Singh Dhillon(Chelsea and Westminster Hospital), Fabiola Martin(University College London), Sarah Russell-Sharpe, Sophie Allan, A. L. Harte, Sue Clay, A Tariq, Horace J. Spencer, Ron Jones, Jessica Pritchard(Royal Free London NHS Foundation Trust), Shirley Cumming, Claire Atkinson, Valérie Delpech
The Lancet HIV
May 4, 2017
Cited by 65Open Access
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Abstract

BACKGROUND: The length of time that people with HIV on antiretroviral therapy (ART) with viral load suppression will be able to continue before developing viral rebound is unknown. We aimed to investigate the rate of first viral rebound in people that have achieved initial suppression with ART, to determine factors associated with viral rebound, and to use these estimates to predict long-term durability of viral suppression. METHODS: The UK Collaborative HIV Cohort (UK CHIC) Study is an ongoing multicentre cohort study that brings together in a standardised format data on people with HIV attending clinics around the UK. We included participants who started ART with three or more drugs and who had achieved viral suppression (≤50 copies per mL) by 9 months after the start of ART (baseline). Viral rebound was defined as the first single viral load of more than 200 copies per mL or treatment interruption (for ≥1 month). We investigated factors associated with viral rebound with Poisson regression. These results were used to calculate the rate of viral rebound according to several key factors, including age, calendar year at start of ART, and time since baseline. RESULTS: Of the 16 101 people included, 4519 had a first viral rebound over 58 038 person-years (7·8 per 100 person-years, 95% CI 7·6-8·0). Of the 4519 viral rebounds, 3105 (69%) were defined by measurement of a single viral load of more than 200 copies per mL, and 1414 (31%) by a documented treatment interruption. The rate of first viral rebound declined substantially over time until 7 years from baseline. The other factors associated with viral rebound were current age at follow-up and calendar year at ART initiation (p<0·0001) and HIV risk group (p<0·0001); higher pre-ART CD4 count (p=0·0008) and pre-ART viral load (p=0·0003) were associated with viral rebound in the multivariate analysis only. For 1322 (29%) of the 3105 people with observed viral rebound, the next viral load value after rebound was 50 copies per mL or less with no regimen change. For HIV-positive men who have sex with men, our estimates suggest that the probability of first viral rebound reaches a plateau of 1·4% per year after 45 years of age, and 1·0% when accounting for the fact that 29% of viral rebounds are temporary elevations. INTERPRETATION: A substantial proportion of people on ART will not have viral rebound over their lifetime, which has implications for people with HIV and the planning of future drug development. FUNDING: UK Medical Research Council.


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