Long-term Patient-Centered Outcomes in Cirrhotic Patients With Chronic Hepatitis C After Achieving Sustained Virologic Response.


Journal

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
ISSN: 1542-7714
Titre abrégé: Clin Gastroenterol Hepatol
Pays: United States
ID NLM: 101160775

Informations de publication

Date de publication:
02 2022
Historique:
received: 21 10 2020
revised: 04 01 2021
accepted: 18 01 2021
pubmed: 26 1 2021
medline: 16 3 2022
entrez: 25 1 2021
Statut: ppublish

Résumé

Achieving sustained virologic response (SVR) among patients with hepatitis C virus (HCV) leads to patient reported outcome (PRO) improvement. We aimed to assess the long-term post-SVR PRO trends in HCV patients with cirrhosis. Patients with HCV and cirrhosis treated in clinical trials with direct acting antiviral agents (DAAs) who achieved SVR-12 were prospectively enrolled in a long-term registry (clinicaltrials.gov #NCT02292706). PROs were collected every 24 weeks using the Short Form-36v2 (SF-36), CLDQ-HCV, and WPAI-HCV. Pre-treatment baseline data were available for 854 cirrhotic patients who achieved SVR after DAAs. Of these, 730 had compensated (CC) and 124 had decompensated cirrhosis (DCC) before treatment- patients with DCC reported severe impairment in their PROs in comparison to CC patients (by mean -5% to -16% of a PRO range size; p < .05 for 16 out of 20 studied PROs]. After achieving SVR and registry enrollment, significant PRO improvements were noted from pre-treatment levels in 11/20 domains for those with DCC (+4% to +21%) and 19/20 PRO domains in patients with CC (+3% to +17%). Patients with baseline DCC had higher rates of hepatocellular carcinoma and mortality (P < .05). In patients with CC, the PRO gains persisted up to 168 weeks (3.5 years) of registry follow-up. In patients with DCC, the improvements lasted for at least 96 weeks but a declining trend after year 2. Patients with HCV cirrhosis experience severe PRO impairment at baseline with sustainable improvement after SVR. Though those with DCC experience improvement, there is a decline after 2 years.

Sections du résumé

BACKGROUND & AIMS
Achieving sustained virologic response (SVR) among patients with hepatitis C virus (HCV) leads to patient reported outcome (PRO) improvement. We aimed to assess the long-term post-SVR PRO trends in HCV patients with cirrhosis.
METHODS
Patients with HCV and cirrhosis treated in clinical trials with direct acting antiviral agents (DAAs) who achieved SVR-12 were prospectively enrolled in a long-term registry (clinicaltrials.gov #NCT02292706). PROs were collected every 24 weeks using the Short Form-36v2 (SF-36), CLDQ-HCV, and WPAI-HCV.
RESULTS
Pre-treatment baseline data were available for 854 cirrhotic patients who achieved SVR after DAAs. Of these, 730 had compensated (CC) and 124 had decompensated cirrhosis (DCC) before treatment- patients with DCC reported severe impairment in their PROs in comparison to CC patients (by mean -5% to -16% of a PRO range size; p < .05 for 16 out of 20 studied PROs]. After achieving SVR and registry enrollment, significant PRO improvements were noted from pre-treatment levels in 11/20 domains for those with DCC (+4% to +21%) and 19/20 PRO domains in patients with CC (+3% to +17%). Patients with baseline DCC had higher rates of hepatocellular carcinoma and mortality (P < .05). In patients with CC, the PRO gains persisted up to 168 weeks (3.5 years) of registry follow-up. In patients with DCC, the improvements lasted for at least 96 weeks but a declining trend after year 2.
CONCLUSIONS
Patients with HCV cirrhosis experience severe PRO impairment at baseline with sustainable improvement after SVR. Though those with DCC experience improvement, there is a decline after 2 years.

Identifiants

pubmed: 33493697
pii: S1542-3565(21)00076-8
doi: 10.1016/j.cgh.2021.01.026
pii:
doi:

Substances chimiques

Antiviral Agents 0
Ribavirin 49717AWG6K
Sofosbuvir WJ6CA3ZU8B

Banques de données

ClinicalTrials.gov
['NCT02292706']

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

438-446

Informations de copyright

Copyright © 2022 AGA Institute. Published by Elsevier Inc. All rights reserved.

Auteurs

Zobair M Younossi (ZM)

Center for Liver Diseases, Department of Medicine, Inova Fairfax Hospital, Falls Church, Virginia; Inova Medicine, Inova Health System, Falls Church, Virginia; Betty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, Virginia. Electronic address: Zobair.Younossi@inova.org.

Andrei Racila (A)

Center for Liver Diseases, Department of Medicine, Inova Fairfax Hospital, Falls Church, Virginia; Inova Medicine, Inova Health System, Falls Church, Virginia.

Andrew Muir (A)

Department of Medicine, Duke University Medical Center, Durham, North Carolina.

Marc Bourliere (M)

Department of Hepato- Gastroenterology, Hospital Saint Joseph, Marseille, France.

Alessandra Mangia (A)

IRCCS Casa Sollievo della Sofferenza Hospital, Liver Unit, Medical Sciences, San Giovanni Rotondo, Italy.

Rafael Esteban (R)

Liver Unit, Hospital Universitari Vall d'Hebron and Ciberehd del Instituto Carlos III, Barcelona, Spain.

Stefan Zeuzem (S)

Department of Medicine I at the Goethe University Hospital, Frankfurt, Germany.

Massimo Colombo (M)

Liver Center for Translational Research, IRCCS Humanitas, Milan, Italy.

Michael Manns (M)

Hannover Medical School, Hannover, Germany.

George V Papatheodoridis (GV)

Academic Gastroenterology Department, Laiko Hospital, Athens, Greece.

Maria Buti (M)

Liver Unit, Hospital Universitari Vall d'Hebron and Ciberehd del Instituto Carlos III, Barcelona, Spain.

Anand Chokkalingam (A)

Gilead Sciences, Foster City, California.

Anuj Gaggar (A)

Gilead Sciences, Foster City, California.

Fatema Nader (F)

Center for Outcomes Research in Liver Disease, Washington, District of Columbia.

Issah Younossi (I)

Center for Outcomes Research in Liver Disease, Washington, District of Columbia.

Linda Henry (L)

Center for Outcomes Research in Liver Disease, Washington, District of Columbia.

Maria Stepanova (M)

Center for Outcomes Research in Liver Disease, Washington, District of Columbia.

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Classifications MeSH