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Real-world Effectiveness of Sofosbuvir/Velpatasvir for Treatment of Chronic Hepatitis C in British Columbia, Canada: A Population-Based Cohort Study

BACKGROUND: Clinical trials show high efficacy of sofosbuvir/velpatasvir (SOF/VEL), but there are limited data from “real-world” settings. We aimed to evaluate SOF/VEL effectiveness for all hepatitis C virus (HCV) genotypes (GTs) in British Columbia (BC), Canada. METHODS: We used the BC Hepatitis Te...

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Autores principales: Wilton, James, Wong, Stanley, Yu, Amanda, Ramji, Alnoor, Cook, Darrel, Butt, Zahid A, Alvarez, Maria, Binka, Mawuena, Darvishian, Maryam, Jeong, Dahn, Bartlett, Sofia R, Pearce, Margo E, Adu, Prince A, Yoshida, Eric M, Krajden, Mel, Janjua, Naveed Z
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052750/
https://www.ncbi.nlm.nih.gov/pubmed/32154326
http://dx.doi.org/10.1093/ofid/ofaa055
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author Wilton, James
Wong, Stanley
Yu, Amanda
Ramji, Alnoor
Cook, Darrel
Butt, Zahid A
Alvarez, Maria
Binka, Mawuena
Darvishian, Maryam
Jeong, Dahn
Bartlett, Sofia R
Pearce, Margo E
Adu, Prince A
Yoshida, Eric M
Krajden, Mel
Janjua, Naveed Z
author_facet Wilton, James
Wong, Stanley
Yu, Amanda
Ramji, Alnoor
Cook, Darrel
Butt, Zahid A
Alvarez, Maria
Binka, Mawuena
Darvishian, Maryam
Jeong, Dahn
Bartlett, Sofia R
Pearce, Margo E
Adu, Prince A
Yoshida, Eric M
Krajden, Mel
Janjua, Naveed Z
author_sort Wilton, James
collection PubMed
description BACKGROUND: Clinical trials show high efficacy of sofosbuvir/velpatasvir (SOF/VEL), but there are limited data from “real-world” settings. We aimed to evaluate SOF/VEL effectiveness for all hepatitis C virus (HCV) genotypes (GTs) in British Columbia (BC), Canada. METHODS: We used the BC Hepatitis Testers Cohort, which includes all HCV cases in the province (1990–2015) linked to administrative databases, including prescriptions to end of 2018. We measured sustained virologic response (SVR; negative RNA ≥10 weeks after treatment end) and identified characteristics associated with non-SVR. Conservatively, we excluded individuals with no assessment for SVR if their last RNA test after treatment initiation was negative (but included if positive). RESULTS: Of 2821 eligible participants, most were infected with GT1 (1076, 38.1%) or GT3 (1072, 38.0%), and a minority (278, 9.9%) were treated with RBV. SVR was 94.6% (2670/2821) overall and 94.5% (1017/1076) for GT1, 96.4% (512/531) for GT2, and 93.7% (1004/1072) for GT3. When disaggregated by GT, treatment regimen, and cirrhosis/treatment experience, SVR was lowest (30/40, 75.0%) among treatment-experienced GT3 individuals treated with RBV. Characteristics associated with non-SVR in multivariable analysis included younger age, RBV addition, and being a person with HIV (PWH) or who injects/injected drugs (PWID). When treatment regimen (±RBV) was removed from multivariable model, treatment experience was associated with non-SVR for GT3. Of 151 non-SVR individuals, 56.3% were nonvirological failures (treatment incomplete/no assessment for SVR) and 43.7% were virological failures (nonresponse/relapse). A disproportionately high percentage of non-SVR among PWID was due to nonvirological failure. CONCLUSIONS: SOF/VEL was highly effective in this “real-world” population-based cohort. Additional support is required for PWID/PWH to reach SVR.
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spelling pubmed-70527502020-03-09 Real-world Effectiveness of Sofosbuvir/Velpatasvir for Treatment of Chronic Hepatitis C in British Columbia, Canada: A Population-Based Cohort Study Wilton, James Wong, Stanley Yu, Amanda Ramji, Alnoor Cook, Darrel Butt, Zahid A Alvarez, Maria Binka, Mawuena Darvishian, Maryam Jeong, Dahn Bartlett, Sofia R Pearce, Margo E Adu, Prince A Yoshida, Eric M Krajden, Mel Janjua, Naveed Z Open Forum Infect Dis Major Article BACKGROUND: Clinical trials show high efficacy of sofosbuvir/velpatasvir (SOF/VEL), but there are limited data from “real-world” settings. We aimed to evaluate SOF/VEL effectiveness for all hepatitis C virus (HCV) genotypes (GTs) in British Columbia (BC), Canada. METHODS: We used the BC Hepatitis Testers Cohort, which includes all HCV cases in the province (1990–2015) linked to administrative databases, including prescriptions to end of 2018. We measured sustained virologic response (SVR; negative RNA ≥10 weeks after treatment end) and identified characteristics associated with non-SVR. Conservatively, we excluded individuals with no assessment for SVR if their last RNA test after treatment initiation was negative (but included if positive). RESULTS: Of 2821 eligible participants, most were infected with GT1 (1076, 38.1%) or GT3 (1072, 38.0%), and a minority (278, 9.9%) were treated with RBV. SVR was 94.6% (2670/2821) overall and 94.5% (1017/1076) for GT1, 96.4% (512/531) for GT2, and 93.7% (1004/1072) for GT3. When disaggregated by GT, treatment regimen, and cirrhosis/treatment experience, SVR was lowest (30/40, 75.0%) among treatment-experienced GT3 individuals treated with RBV. Characteristics associated with non-SVR in multivariable analysis included younger age, RBV addition, and being a person with HIV (PWH) or who injects/injected drugs (PWID). When treatment regimen (±RBV) was removed from multivariable model, treatment experience was associated with non-SVR for GT3. Of 151 non-SVR individuals, 56.3% were nonvirological failures (treatment incomplete/no assessment for SVR) and 43.7% were virological failures (nonresponse/relapse). A disproportionately high percentage of non-SVR among PWID was due to nonvirological failure. CONCLUSIONS: SOF/VEL was highly effective in this “real-world” population-based cohort. Additional support is required for PWID/PWH to reach SVR. Oxford University Press 2020-02-29 /pmc/articles/PMC7052750/ /pubmed/32154326 http://dx.doi.org/10.1093/ofid/ofaa055 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Article
Wilton, James
Wong, Stanley
Yu, Amanda
Ramji, Alnoor
Cook, Darrel
Butt, Zahid A
Alvarez, Maria
Binka, Mawuena
Darvishian, Maryam
Jeong, Dahn
Bartlett, Sofia R
Pearce, Margo E
Adu, Prince A
Yoshida, Eric M
Krajden, Mel
Janjua, Naveed Z
Real-world Effectiveness of Sofosbuvir/Velpatasvir for Treatment of Chronic Hepatitis C in British Columbia, Canada: A Population-Based Cohort Study
title Real-world Effectiveness of Sofosbuvir/Velpatasvir for Treatment of Chronic Hepatitis C in British Columbia, Canada: A Population-Based Cohort Study
title_full Real-world Effectiveness of Sofosbuvir/Velpatasvir for Treatment of Chronic Hepatitis C in British Columbia, Canada: A Population-Based Cohort Study
title_fullStr Real-world Effectiveness of Sofosbuvir/Velpatasvir for Treatment of Chronic Hepatitis C in British Columbia, Canada: A Population-Based Cohort Study
title_full_unstemmed Real-world Effectiveness of Sofosbuvir/Velpatasvir for Treatment of Chronic Hepatitis C in British Columbia, Canada: A Population-Based Cohort Study
title_short Real-world Effectiveness of Sofosbuvir/Velpatasvir for Treatment of Chronic Hepatitis C in British Columbia, Canada: A Population-Based Cohort Study
title_sort real-world effectiveness of sofosbuvir/velpatasvir for treatment of chronic hepatitis c in british columbia, canada: a population-based cohort study
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052750/
https://www.ncbi.nlm.nih.gov/pubmed/32154326
http://dx.doi.org/10.1093/ofid/ofaa055
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