Abstract
Background: Reinfection after successful treatment with direct-acting antivirals is hypothesised to undermine efforts to eliminate hepatitis C virus (HCV) infection among people with HIV. We aimed to assess changes in incidence of HCV reinfection among people with HIV following the introduction of direct-acting antivirals, and the proportion of all incident cases attributable to reinfection. Methods: We pooled individual-level data on HCV reinfection in people with HIV after spontaneous or treatment-induced clearance of HCV from six cohorts contributing data to the International Collaboration on Hepatitis C Elimination in HIV Cohorts (InCHEHC) in Australia, Canada, France, the Netherlands, Spain, and Switzerland between Jan 1, 2010, and Dec 31, 2019. Participants were eligible if they had evidence of an HCV infection (HCV antibody or RNA positive test) followed by spontaneous clearance or treatment-induced clearance, with at least one HCV RNA test after clearance enabling measurement of reinfection. We assessed differences in first reinfection incidence between direct-acting antiviral access periods (pre-direct-acting antiviral, limited access [access restricted to people with moderate or severe liver disease and other priority groups], and broad access [access for all patients with chronic HCV]) using Poisson regression. We estimated changes in combined HCV incidence (primary and reinfection) and the relative contribution of infection type by calendar year. Findings: Overall, 6144 people with HIV who were at risk of HCV reinfection (median age 49 years [IQR 42–54]; 4989 [81%] male; 2836 [46%] men who have sex with men; 2360 [38%] people who inject drugs) were followed up for 17 303 person-years and were included in this analysis. The incidence of first HCV reinfection was stable during the period before the introduction of direct-acting antivirals (pre-introduction period; 4·1 cases per 100 person-years, 95% CI 2·8–6·0). Compared with the pre-introduction period, the average incidence of reinfection was 4% lower during the period of limited access (incidence rate ratio [IRR] 0·96, 95% CI 0·78–1·19), and 28% lower during the period of broad access (0·72, 0·60–0·86). Between 2015 and 2019, the proportion of incident HCV infections due to reinfection increased, but combined incidence declined by 34%, from 1·02 cases per 100 person-years (95% CI 0·96–1·07) in 2015 to 0·67 cases per 100 person-years (95% CI 0·59–0·75) in 2019. Interpretation: HCV reinfection incidence and combined incidence declined in people with HIV following direct-acting antiviral introduction, suggesting reinfection has not affected elimination efforts among people with HIV in InCHEHC countries. The proportion of incident HCV cases due to reinfection was highest during periods of broad access to direct-acting antivirals, highlighting the importance of reducing ongoing risks and continuing testing in people at risk. Funding: Australian National Health and Medical Research Council.
Original language | English |
---|---|
Pages (from-to) | e106-e116 |
Number of pages | 12 |
Journal | The Lancet HIV |
Volume | 11 |
Issue number | 2 |
DOIs | |
Publication status | Published - Feb 2024 |
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In: The Lancet HIV, Vol. 11, No. 2, 02.2024, p. e106-e116.
Research output: Contribution to journal › Article › Research › peer-review
TY - JOUR
T1 - Changes in incidence of hepatitis C virus reinfection and access to direct-acting antiviral therapies in people with HIV from six countries, 2010–19
T2 - an analysis of data from a consortium of prospective cohort studies
AU - Sacks-Davis, Rachel
AU - van Santen, Daniela K.
AU - Boyd, Anders
AU - Young, Jim
AU - Stewart, Ashleigh
AU - Doyle, Joseph S.
AU - Rauch, Andri
AU - Mugglin, Catrina
AU - Klein, Marina
AU - van der Valk, Marc
AU - Smit, Colette
AU - Jarrin, Inmaculada
AU - Berenguer, Juan
AU - Lacombe, Karine
AU - Requena, Maria Bernarda
AU - Wittkop, Linda
AU - Leleux, Olivier
AU - Bonnet, Fabrice
AU - Salmon, Dominique
AU - Matthews, Gail
AU - Guy, Rebecca
AU - Martin, Natasha K.
AU - Spelman, Tim
AU - Prins, Maria
AU - Stoove, Mark
AU - Hellard, Margaret E.
AU - on behalf of the InCHEHC Collaboration
N1 - Funding Information: The authors thank the study participants for their contribution to the research. The authors acknowledge the contribution of the ACCESS team members and ACCESS advisory committee members who are not coauthors of this article. The authors also acknowledge all clinical services participating in ACCESS. The list of ACCESS team members, advisory committee members, and participating services can be found on the ACCESS website. ACCESS is a partnership between the Burnet Institute, Kirby Institute, and National Reference Laboratory. The ATHENA database is maintained by Stichting HIV Monitoring and supported by a grant from the Dutch Ministry of Health, Welfare and Sport through the Centre for Infectious Disease Control of the National Institute for Public Health and the Environment. The authors acknowledge the contribution of the Swiss HIV Cohort Study (SHCS) participants and team members. This study has been financed within the framework of the SHCS, supported by the Swiss National Science Foundation (grant 201369) and by the SHCS research foundation. Data from the SHCS are gathered by the Five Swiss University Hospitals, two Cantonal Hospitals, 15 affiliated hospitals, and 36 private physicians. The authors would like to thank all clinicians and clinical research technicians participating in the SAIDCC database of the Infectious Diseases Unit of St Antoine Hospital (Paris, France). We acknowledge the contribution of the AQUITAINE scientific committee. We also acknowledge the ANRS CO3 Aquitaine/AquiVIH-NA Cohort participants, the study coordinators, the central coordinating team, and nurses for their assistance with study coordination, participant recruitment, and care. The ANRS CO3 Aquitaine cohort is supported by the ANRS Emerging Infectious Diseases and the Bordeaux University Hospital Centre. The authors acknowledge the CoRIS Executive Committee and the centres and investigators involved in the CoRIS cohort. The CoRIS cohort is supported by CIBER – Consorcio Centro de Investigación Biomédica en Red – (CB21/13/00091), Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación and Unión Europea – NextGenerationEU. We acknowledge the contribution of the Scientific Committee of the ANRS CO13 HEPAVIH including representatives of the sponsor (clinical research and pharmacovigilance department) and representatives of patient organisations including TRT5. We also acknowledge the ANRS CO13 HEPAVIH cohort participants, the study coordinators, the central coordinating team, and nurses for their assistance with study coordination, participant recruitment, and care. The ANRS CO13 Hepavih cohort is supported by the ANRS Emerging Infectious Diseases. We acknowledge the Canadian Coinfection Cohort (CCC) steering committee members, central coordinating staff, study participants, and community advisers. We also acknowledge Canadian Coinfection Cohort coinvestigators, study coordinators, and nurses for their assistance with study coordination, participant recruitment, and care. The Canadian Coinfection Cohort is supported by Fonds de recherche du Québec-Santé; the Canadian Institute for Health Research (CIHR; FDN-143270); and the CIHR Canadian HIV Trials Network (CTN222). We would also like to acknowledge Campbell Aitken for English language editing of the manuscript text. This study was funded by the Australian Government National Health and Medical Research Council (grant numbers GNT1132902 and GNT2020121). We gratefully acknowledge the contribution to this work of the Victorian Operational Infrastructure Support Program received by the Burnet Institute. Funding Information: The authors thank the study participants for their contribution to the research. The authors acknowledge the contribution of the ACCESS team members and ACCESS advisory committee members who are not coauthors of this article. The authors also acknowledge all clinical services participating in ACCESS. The list of ACCESS team members, advisory committee members, and participating services can be found on the ACCESS website. ACCESS is a partnership between the Burnet Institute, Kirby Institute, and National Reference Laboratory. The ATHENA database is maintained by Stichting HIV Monitoring and supported by a grant from the Dutch Ministry of Health, Welfare and Sport through the Centre for Infectious Disease Control of the National Institute for Public Health and the Environment. The authors acknowledge the contribution of the Swiss HIV Cohort Study (SHCS) participants and team members . This study has been financed within the framework of the SHCS, supported by the Swiss National Science Foundation (grant 201369) and by the SHCS research foundation. Data from the SHCS are gathered by the Five Swiss University Hospitals, two Cantonal Hospitals, 15 affiliated hospitals, and 36 private physicians. The authors would like to thank all clinicians and clinical research technicians participating in the SAIDCC database of the Infectious Diseases Unit of St Antoine Hospital (Paris, France). We acknowledge the contribution of the AQUITAINE scientific committee. We also acknowledge the ANRS CO3 Aquitaine/AquiVIH-NA Cohort participants, the study coordinators, the central coordinating team, and nurses for their assistance with study coordination, participant recruitment, and care. The ANRS CO3 Aquitaine cohort is supported by the ANRS Emerging Infectious Diseases and the Bordeaux University Hospital Centre. The authors acknowledge the CoRIS Executive Committee and the centres and investigators involved in the CoRIS cohort . The CoRIS cohort is supported by CIBER – Consorcio Centro de Investigación Biomédica en Red – (CB21/13/00091), Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación and Unión Europea – NextGenerationEU. We acknowledge the contribution of the Scientific Committee of the ANRS CO13 HEPAVIH including representatives of the sponsor (clinical research and pharmacovigilance department) and representatives of patient organisations including TRT5. We also acknowledge the ANRS CO13 HEPAVIH cohort participants, the study coordinators, the central coordinating team, and nurses for their assistance with study coordination, participant recruitment, and care. The ANRS CO13 Hepavih cohort is supported by the ANRS Emerging Infectious Diseases. We acknowledge the Canadian Coinfection Cohort (CCC) steering committee members, central coordinating staff, study participants, and community advisers. We also acknowledge Canadian Coinfection Cohort coinvestigators, study coordinators, and nurses for their assistance with study coordination, participant recruitment, and care. The Canadian Coinfection Cohort is supported by Fonds de recherche du Québec-Santé; the Canadian Institute for Health Research (CIHR; FDN-143270); and the CIHR Canadian HIV Trials Network (CTN222). We would also like to acknowledge Campbell Aitken for English language editing of the manuscript text. This study was funded by the Australian Government National Health and Medical Research Council (grant numbers GNT1132902 and GNT2020121). We gratefully acknowledge the contribution to this work of the Victorian Operational Infrastructure Support Program received by the Burnet Institute. Publisher Copyright: © 2024 Elsevier Ltd
PY - 2024/2
Y1 - 2024/2
N2 - Background: Reinfection after successful treatment with direct-acting antivirals is hypothesised to undermine efforts to eliminate hepatitis C virus (HCV) infection among people with HIV. We aimed to assess changes in incidence of HCV reinfection among people with HIV following the introduction of direct-acting antivirals, and the proportion of all incident cases attributable to reinfection. Methods: We pooled individual-level data on HCV reinfection in people with HIV after spontaneous or treatment-induced clearance of HCV from six cohorts contributing data to the International Collaboration on Hepatitis C Elimination in HIV Cohorts (InCHEHC) in Australia, Canada, France, the Netherlands, Spain, and Switzerland between Jan 1, 2010, and Dec 31, 2019. Participants were eligible if they had evidence of an HCV infection (HCV antibody or RNA positive test) followed by spontaneous clearance or treatment-induced clearance, with at least one HCV RNA test after clearance enabling measurement of reinfection. We assessed differences in first reinfection incidence between direct-acting antiviral access periods (pre-direct-acting antiviral, limited access [access restricted to people with moderate or severe liver disease and other priority groups], and broad access [access for all patients with chronic HCV]) using Poisson regression. We estimated changes in combined HCV incidence (primary and reinfection) and the relative contribution of infection type by calendar year. Findings: Overall, 6144 people with HIV who were at risk of HCV reinfection (median age 49 years [IQR 42–54]; 4989 [81%] male; 2836 [46%] men who have sex with men; 2360 [38%] people who inject drugs) were followed up for 17 303 person-years and were included in this analysis. The incidence of first HCV reinfection was stable during the period before the introduction of direct-acting antivirals (pre-introduction period; 4·1 cases per 100 person-years, 95% CI 2·8–6·0). Compared with the pre-introduction period, the average incidence of reinfection was 4% lower during the period of limited access (incidence rate ratio [IRR] 0·96, 95% CI 0·78–1·19), and 28% lower during the period of broad access (0·72, 0·60–0·86). Between 2015 and 2019, the proportion of incident HCV infections due to reinfection increased, but combined incidence declined by 34%, from 1·02 cases per 100 person-years (95% CI 0·96–1·07) in 2015 to 0·67 cases per 100 person-years (95% CI 0·59–0·75) in 2019. Interpretation: HCV reinfection incidence and combined incidence declined in people with HIV following direct-acting antiviral introduction, suggesting reinfection has not affected elimination efforts among people with HIV in InCHEHC countries. The proportion of incident HCV cases due to reinfection was highest during periods of broad access to direct-acting antivirals, highlighting the importance of reducing ongoing risks and continuing testing in people at risk. Funding: Australian National Health and Medical Research Council.
AB - Background: Reinfection after successful treatment with direct-acting antivirals is hypothesised to undermine efforts to eliminate hepatitis C virus (HCV) infection among people with HIV. We aimed to assess changes in incidence of HCV reinfection among people with HIV following the introduction of direct-acting antivirals, and the proportion of all incident cases attributable to reinfection. Methods: We pooled individual-level data on HCV reinfection in people with HIV after spontaneous or treatment-induced clearance of HCV from six cohorts contributing data to the International Collaboration on Hepatitis C Elimination in HIV Cohorts (InCHEHC) in Australia, Canada, France, the Netherlands, Spain, and Switzerland between Jan 1, 2010, and Dec 31, 2019. Participants were eligible if they had evidence of an HCV infection (HCV antibody or RNA positive test) followed by spontaneous clearance or treatment-induced clearance, with at least one HCV RNA test after clearance enabling measurement of reinfection. We assessed differences in first reinfection incidence between direct-acting antiviral access periods (pre-direct-acting antiviral, limited access [access restricted to people with moderate or severe liver disease and other priority groups], and broad access [access for all patients with chronic HCV]) using Poisson regression. We estimated changes in combined HCV incidence (primary and reinfection) and the relative contribution of infection type by calendar year. Findings: Overall, 6144 people with HIV who were at risk of HCV reinfection (median age 49 years [IQR 42–54]; 4989 [81%] male; 2836 [46%] men who have sex with men; 2360 [38%] people who inject drugs) were followed up for 17 303 person-years and were included in this analysis. The incidence of first HCV reinfection was stable during the period before the introduction of direct-acting antivirals (pre-introduction period; 4·1 cases per 100 person-years, 95% CI 2·8–6·0). Compared with the pre-introduction period, the average incidence of reinfection was 4% lower during the period of limited access (incidence rate ratio [IRR] 0·96, 95% CI 0·78–1·19), and 28% lower during the period of broad access (0·72, 0·60–0·86). Between 2015 and 2019, the proportion of incident HCV infections due to reinfection increased, but combined incidence declined by 34%, from 1·02 cases per 100 person-years (95% CI 0·96–1·07) in 2015 to 0·67 cases per 100 person-years (95% CI 0·59–0·75) in 2019. Interpretation: HCV reinfection incidence and combined incidence declined in people with HIV following direct-acting antiviral introduction, suggesting reinfection has not affected elimination efforts among people with HIV in InCHEHC countries. The proportion of incident HCV cases due to reinfection was highest during periods of broad access to direct-acting antivirals, highlighting the importance of reducing ongoing risks and continuing testing in people at risk. Funding: Australian National Health and Medical Research Council.
UR - http://www.scopus.com/inward/record.url?scp=85183338183&partnerID=8YFLogxK
U2 - 10.1016/S2352-3018(23)00267-9
DO - 10.1016/S2352-3018(23)00267-9
M3 - Article
C2 - 38224708
AN - SCOPUS:85183338183
SN - 2405-4704
VL - 11
SP - e106-e116
JO - The Lancet HIV
JF - The Lancet HIV
IS - 2
ER -