Efficacy of ultra-short, response-guided sofosbuvir and daclatasvir therapy for Hepatitis C: a single arm mechanistic pilot study

Author:

Flower BarnabyORCID,Hung Le Manh,McCabe Leanne,Ansari M. Azim,Le Ngoc Chau,Vo Thi Thu,Vu Thi Kim Hang,Nguyen Thi Ngoc Phuong,Phuong Le Thanh,Quang Vo Minh,Trong Thuan Dang,Le Thi Thao,Bao Tran Nguyen,Kingsley Cherry,Smith David,Hoglund Richard M.,Tarning JoelORCID,Kestelyn EvelyneORCID,Pett Sarah L,van Doorn Rogier,van Nuil Jennifer Ilo,Turner Hugo,Thwaites GuyORCID,Barnes Eleanor,Rahman Motiur,Walker Ann SarahORCID,Day JeremyORCID,Van Vinh Chau Nguyen,Cooke Graham S

Abstract

ABSTRACTBackgroundWHO has called for research into predictive factors for selecting persons who could be successfully treated with shorter durations of direct acting antiviral (DAA) therapy for Hepatitis C. We evaluated early virological response as a means of shortening treatment and explored host, viral and pharmacokinetic contributors to treatment outcome.MethodsDuration of sofosbuvir and daclatasvir (SOF/DCV) was determined according to day 2 (D2) virologic response for HCV genotype (gt) 1- or 6-infected adults in Vietnam with mild liver disease. Participants received 4 or 8 weeks treatment according to whether D2 HCV RNA was above or below 500 IU/ml (standard duration is 12 weeks). Primary endpoint was sustained virological response (SVR12). Those failing therapy were retreated with 12 weeks SOF/DCV. Host IFNL4 genotype and viral sequencing was performed at baseline, with repeat viral sequencing if virological rebound was observed. Levels of SOF, its inactive metabolite GS-331007 and DCV were measured on day 0 and 28.ResultsOf 52 adults enrolled, 34 received 4 weeks SOF/DCV, 17 got 8 weeks and one withdrew. SVR12 was achieved in 21/34 (62%) treated for 4 weeks, and 17/17 (100%) treated for 8 weeks. Overall 38/51 (75%) were cured with first-line treatment (mean duration 37 days). Despite a high prevalence of putative NS5A-inhibitor resistance associated substitutions (RAS), all first-line treatment failures cured after retreatment (13/13). We found no evidence treatment failure was associated with host IFNL4 genotype, viral subtype, baseline RAS or DCV levels. SOF metabolite levels were higher in those failing 4-week therapy.ConclusionsShortened SOF/DCV therapy, with retreatment if needed, reduces DAA use while maintaining high cure rates. D2 virologic response alone does not adequately predict SVR12 with 4 weeks treatment.FundingFunded by the Medical Research Council (grant MR/P025064/1) and The Global Challenges Research Fund (Wellcome Trust Grant 206/296/Z/17/Z).)Clinical trial numberISRCTN17100273

Publisher

Cold Spring Harbor Laboratory

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