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JAMA· 2012Q1

Association Between Sustained Virological Response and All-Cause Mortality Among Patients With Chronic Hepatitis C and Advanced Hepatic Fibrosis

Adriaan J. van der Meer, Bart J. Veldt, Jordan J. Feld, Heiner Wedemeyer et al.

Short summary

Achieving a sustained virological response (SVR) to interferon-based treatment for chronic Hepatitis C (HCV) with advanced fibrosis significantly reduces the risk of all-cause mortality by 74% (HR, 0.26) and liver-related death or transplantation by 94% (HR, 0.06).

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Key points

  • Sustained virological response (SVR) to interferon-based treatment was achieved by 36% (192/530) of patients with chronic HCV and advanced fibrosis.
  • The 10-year cumulative all-cause mortality rate was 8.9% for patients with SVR compared to 26.0% for those without SVR (P < .001).
  • SVR was associated with a 74% reduced risk of all-cause mortality (HR, 0.26; P < .001) and a 94% reduced risk of liver-related mortality or transplantation (HR, 0.06; P < .001).
  • 10-year cumulative incidence of HCC was 5.1% with SVR vs. 21.8% without; liver failure was 2.1% with SVR vs. 29.9% without.

AI-generated from the title and abstract; the full text is not read.

Abstract

CONTEXT: Chronic hepatitis C virus (HCV) infection outcomes include liver failure, hepatocellular carcinoma (HCC), and liver-related death. OBJECTIVE: To assess the association between sustained virological response (SVR) and all-cause mortality in patients with chronic HCV infection and advanced hepatic fibrosis. DESIGN, SETTING, AND PATIENTS: An international, multicenter, long-term follow-up study from 5 large tertiary care hospitals in Europe and Canada of 530 patients with chronic HCV infection who started an interferon-based treatment regimen between 1990 and 2003, following histological proof of advanced hepatic fibrosis or cirrhosis (Ishak score 4-6). Complete follow-up ranged between January 2010 and October 2011. MAIN OUTCOME MEASURES: All-cause mortality. Secondary outcomes were liver failure, HCC, and liver-related mortality or liver transplantation. RESULTS: The 530 study patients were followed up for a median (interquartile range [IQR]) of 8.4 (6.4-11.4) years. The baseline median (IQR) age was 48 (42-56) years and 369 patients (70%) were men. The Ishak fibrosis score was 4 in 143 patients (27%), 5 in 101 patients (19%), and 6 in 286 patients (54%). There were 192 patients (36%) who achieved SVR; 13 patients with SVR and 100 without SVR died (10-year cumulative all-cause mortality rate, 8.9% [95% CI, 3.3%-14.5%] with SVR and 26.0% [95% CI, 20.2%-28.4%] without SVR; P < .001). In time-dependent multivariate Cox regression analysis, SVR was associated with reduced risk of all-cause mortality (hazard ratio [HR], 0.26; 95% CI, 0.14-0.49; P < .001) and reduced risk of liver-related mortality or transplantation (HR, 0.06; 95% CI, 0.02-0.19; P < .001), the latter occurring in 3 patients with SVR and 103 without SVR. The 10-year cumulative incidence rate of liver-related mortality or transplantation was 1.9% (95% CI, 0.0%-4.1%) with SVR and 27.4% (95% CI, 22.0%-32.8%) without SVR (P < .001). There were 7 patients with SVR and 76 without SVR who developed HCC (10-year cumulative incidence rate, 5.1%; 95% CI, 1.3%-8.9%; vs 21.8%; 95% CI, 16.6%-27.0%; P < .001), and 4 patients with SVR and 111 without SVR experienced liver failure (10-year cumulative incidence rate, 2.1%; 95% CI, 0.0%-4.5%; vs 29.9%; 95% CI, 24.3%-35.5%; P < .001). CONCLUSION: Among patients with chronic HCV infection and advanced hepatic fibrosis, sustained virological response to interferon-based treatment was associated with lower all-cause mortality.

The authors' abstract, as published at the source. JAMA, 2012 · DOI ↗

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Field: Hepatology

HepatologyMedicine