Direct-Acting Antiviral Therapy for Hepatitis C Virus Infection Is Associated With Increased Survival in Patients With a History of Hepatocellular Carcinoma.


Journal

Gastroenterology
ISSN: 1528-0012
Titre abrégé: Gastroenterology
Pays: United States
ID NLM: 0374630

Informations de publication

Date de publication:
11 2019
Historique:
received: 24 03 2019
revised: 24 06 2019
accepted: 22 07 2019
pubmed: 3 8 2019
medline: 20 12 2019
entrez: 3 8 2019
Statut: ppublish

Résumé

There is controversy regarding the benefits of direct-acting antiviral (DAA) therapy for hepatitis C virus (HCV) infection for patients with a history of hepatocellular carcinoma (HCC). We performed a multicenter cohort study to compare overall survival between patients with HCV infection treated with DAAs and patients who did not receive DAA treatment for their HCV infection after complete response to prior HCC therapy. We conducted a retrospective cohort study of patients with HCV-related HCC who achieved a complete response to resection, local ablation, transarterial chemo- or radioembolization, or radiation therapy, from January 2013 through December 2017 at 31 health care systems throughout the United States and Canada. We used Cox proportional hazards regression to determine the association between receipt of DAA therapy, modeled as a time-varying covariate, and all-cause mortality, accounting for informative censoring and confounding using inverse probability weighting. Of 797 patients with HCV-related HCC, 383 (48.1%) received DAA therapy and 414 (51.9%) did not receive treatment for their HCV infection after complete response to prior HCC therapy. Among DAA-treated patients, 43 deaths occurred during 941 person-years of follow-up, compared with 103 deaths during 526.6 person-years of follow-up among patients who did not receive DAA therapy (crude rate ratio, 0.23; 95% confidence interval [CI], 0.16-0.33). In inverse probability-weighted analyses, DAA therapy was associated with a significant reduction in risk of death (hazard ratio, 0.54; 95% CI, 0.33-0.90). This association differed by sustained virologic response to DAA therapy; risk of death was reduced in patients with sustained virologic response to DAA therapy (hazard ratio, 0.29; 95% CI, 0.18-0.47), but not in patients without a sustained virologic response (hazard ratio, 1.13; 95% CI, 0.55-2.33). In an analysis of nearly 800 patients with complete response to HCC treatment, DAA therapy was associated with a significant reduction in risk of death.

Sections du résumé

BACKGROUND & AIMS
There is controversy regarding the benefits of direct-acting antiviral (DAA) therapy for hepatitis C virus (HCV) infection for patients with a history of hepatocellular carcinoma (HCC). We performed a multicenter cohort study to compare overall survival between patients with HCV infection treated with DAAs and patients who did not receive DAA treatment for their HCV infection after complete response to prior HCC therapy.
METHODS
We conducted a retrospective cohort study of patients with HCV-related HCC who achieved a complete response to resection, local ablation, transarterial chemo- or radioembolization, or radiation therapy, from January 2013 through December 2017 at 31 health care systems throughout the United States and Canada. We used Cox proportional hazards regression to determine the association between receipt of DAA therapy, modeled as a time-varying covariate, and all-cause mortality, accounting for informative censoring and confounding using inverse probability weighting.
RESULTS
Of 797 patients with HCV-related HCC, 383 (48.1%) received DAA therapy and 414 (51.9%) did not receive treatment for their HCV infection after complete response to prior HCC therapy. Among DAA-treated patients, 43 deaths occurred during 941 person-years of follow-up, compared with 103 deaths during 526.6 person-years of follow-up among patients who did not receive DAA therapy (crude rate ratio, 0.23; 95% confidence interval [CI], 0.16-0.33). In inverse probability-weighted analyses, DAA therapy was associated with a significant reduction in risk of death (hazard ratio, 0.54; 95% CI, 0.33-0.90). This association differed by sustained virologic response to DAA therapy; risk of death was reduced in patients with sustained virologic response to DAA therapy (hazard ratio, 0.29; 95% CI, 0.18-0.47), but not in patients without a sustained virologic response (hazard ratio, 1.13; 95% CI, 0.55-2.33).
CONCLUSIONS
In an analysis of nearly 800 patients with complete response to HCC treatment, DAA therapy was associated with a significant reduction in risk of death.

Identifiants

pubmed: 31374215
pii: S0016-5085(19)41137-2
doi: 10.1053/j.gastro.2019.07.040
pmc: PMC6815711
mid: NIHMS1535996
pii:
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Comparative Study Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1253-1263.e2

Subventions

Organisme : NCI NIH HHS
ID : R01 CA222900
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2019 AGA Institute. Published by Elsevier Inc. All rights reserved.

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Auteurs

Amit G Singal (AG)

Division of Digestive and Liver Disease, UT Southwestern Medical Center, Dallas, Texas. Electronic address: amit.singal@utsouthwestern.edu.

Nicole E Rich (NE)

Division of Digestive and Liver Disease, UT Southwestern Medical Center, Dallas, Texas.

Neil Mehta (N)

Division of Gastroenterology, University of California San Francisco, San Francisco, California.

Andrea D Branch (AD)

Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.

Anjana Pillai (A)

Division of Gastroenterology, Hepatology and Nutrition, University of Chicago, Chicago, Illinois.

Maarouf Hoteit (M)

Division of Gastroenterology and Hepatology, University of Pennsylvania, Philadelphia, Pennsylvania.

Michael Volk (M)

Transplantation Institute and Division of Gastroenterology, Loma Linda University Health, Loma Linda, California.

Mobolaji Odewole (M)

Division of Digestive and Liver Disease, UT Southwestern Medical Center, Dallas, Texas.

Steven Scaglione (S)

Division of Hepatology, Loyola University Medical Center and Edward Hines Veterans Affairs, Hines, Illinois.

Jennifer Guy (J)

Department of Transplantation, California Pacific Medical Center, San Francisco, California.

Adnan Said (A)

Division of Gastroenterology and Hepatology, University of Wisconsin School of Medicine, Madison, Wisconsin.

Jordan J Feld (JJ)

Toronto Center for Liver Disease, Toronto General Hospital, Toronto, Ontario, Canada.

Binu V John (BV)

Division of Gastroenterology and Hepatology, McGuire VA Medical Center, Richmond, Virginia.

Catherine Frenette (C)

Division of Organ Transplantation, Scripps Green Hospital, San Diego, California.

Parvez Mantry (P)

Liver Institute at Methodist Dallas, Dallas, Texas.

Amol S Rangnekar (AS)

Division of Gastroenterology, Georgetown University Hospital, Washington, District of Columbia.

Omobonike Oloruntoba (O)

Division of Gastroenterology and Hepatology, Duke University Health Center, Durham, North Carolina.

Michael Leise (M)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.

Janice H Jou (JH)

Division of Gastroenterology and Hepatology, Oregon Health and Science University, Portland, Oregon.

Kalyan Ram Bhamidimarri (KR)

Division of Hepatology, University of Miami Miller School or Medicine, Miami, Florida.

Laura Kulik (L)

Division of Hepatology, Northwestern University, Chicago, Illinois.

George N Ioannou (GN)

Division of Gastroenterology and Research and Development, Veterans Affairs Puget Sound Healthcare System and University of Washington, Seattle, Washington.

Annsa Huang (A)

Division of Gastroenterology, University of California San Francisco, San Francisco, California.

Tram Tran (T)

Liver Disease and Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California.

Hrishikesh Samant (H)

Division of Gastroenterology and Hepatology, Louisiana State University Health Sciences Center, New Orleans, Louisiana.

Renumathy Dhanasekaran (R)

Division of Gastroenterology and Hepatology, Stanford University, Stanford, California.

Andres Duarte-Rojo (A)

Division of Gastroenterology and Hepatology, University of Arkansas for Medical Sciences, Little Rock, Arkansas.

Reena Salgia (R)

Division of Gastroenterology and Hepatology, Henry Ford Hospital, Detroit, Michigan.

Sheila Eswaran (S)

Division of Gastroenterology, Rush Medical College, Chicago, Illinois.

Prasun Jalal (P)

Division of Abdominal Transplantation, Baylor College of Medicine, Houston, Texas.

Avegail Flores (A)

Division of Gastroenterology, Washington University School of Medicine, St Louis, Missouri.

Sanjaya K Satapathy (SK)

Division of Hepatology, Donald and Barbara Zucker School of Medicine, Northshore University Hospital, Northwell Health, Manhasset, New York.

Sofia Kagan (S)

Division of Digestive and Liver Disease, UT Southwestern Medical Center, Dallas, Texas.

Purva Gopal (P)

Department of Pathology, UT Southwestern Medical Center, Dallas, Texas.

Robert Wong (R)

Division of Gastroenterology and Hepatology, Alameda Health System, Oakland, California.

Neehar D Parikh (ND)

Division of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, Michigan.

Caitlin C Murphy (CC)

Division of Digestive and Liver Disease, UT Southwestern Medical Center, Dallas, Texas.

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