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

Author:

Wilton James1ORCID,Wong Stanley1,Yu Amanda1,Ramji Alnoor2,Cook Darrel1,Butt Zahid A13,Alvarez Maria1,Binka Mawuena1,Darvishian Maryam145,Jeong Dahn16,Bartlett Sofia R178,Pearce Margo E16,Adu Prince A16,Yoshida Eric M2,Krajden Mel17,Janjua Naveed Z16

Affiliation:

1. British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada

2. Division of Gastroenterology, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada

3. School of Public Health and Health Systems, University of Waterloo, Waterloo, Ontario, Canada

4. Cancer Control Research, BC Cancer Research Center, Vancouver, British Columbia, Canada

5. Population Oncology, BC Cancer Research Center, Vancouver, British Columbia, Canada

6. School of Population and Public Health, University of British Columbia, Vancouver, British Columbia, Canada

7. Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada

8. Kirby Institute, University of New South Wales, Sydney, New South Wales, Australia

Abstract

Abstract 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.

Funder

Canadian Institutes of Health Research

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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