Excess mortality in patients with advanced chronic hepatitis C treated with long‐term peginterferon

Chronic hepatitis C virus infection can cause chronic liver disease, cirrhosis and liver cancer. The Hepatitis C Antiviral Long‐term Treatment against Cirrhosis (HALT‐C) Trial was a prospective, randomized controlled study of long‐term, low‐dose peginterferon therapy in patients with advanced chronic hepatitis C who failed to respond to a previous course of optimal antiviral therapy. The aim of this follow‐up analysis is to describe the frequency and causes of death among this cohort of patients. Deaths occurring during and after the HALT‐C Trial were reviewed by a committee of investigators to determine the cause of death and to categorize each death as liver‐ or nonliver‐related and as related or not to complications of peginterferon. Rates of liver transplantation were also assessed. Over a median of 5.7 years, 122 deaths occurred among 1,050 randomized patients (12%), of which 76 were considered liver‐related (62%) and 46 nonliver‐related (38%); 74 patients (7%) underwent liver transplantation. At 7 years the cumulative mortality rate was higher in the treatment compared to the control group (20% versus 15%, P = 0.049); the primary difference in mortality was in patients in the fibrosis compared to the cirrhosis stratum (14% versus 7%, P = 0.01); comparable differences were observed when liver transplantation was included. Excess mortality, emerging after 3 years of treatment, was related largely to nonliver‐related death; liver‐related mortality was similar in the treatment and control groups. No specific cause of death accounted for the excess mortality and only one death was suspected to be a direct complication of peginterferon. Conclusion: Long‐term maintenance peginterferon in patients with advanced chronic hepatitis C is associated with an excess overall mortality, which was primarily due to nonliver‐related causes among patients with bridging fibrosis. (HEPATOLOGY 2011;)

[1]  William M. Lee,et al.  Maintenance peginterferon therapy and other factors associated with hepatocellular carcinoma in patients with advanced hepatitis C. , 2011, Gastroenterology.

[2]  G. Foster,et al.  Systematic review: outcome of compensated cirrhosis due to chronic hepatitis C infection , 2010, Alimentary pharmacology & therapeutics.

[3]  N. Toshikuni,et al.  Comparison of outcomes between patients with alcoholic cirrhosis and those with hepatitis C virus‐related cirrhosis , 2009, Journal of gastroenterology and hepatology.

[4]  M. Ghany,et al.  Diagnosis, management, and treatment of hepatitis C: An update , 2009, Hepatology.

[5]  D. Lavanchy,et al.  The global burden of hepatitis C , 2009, Liver international : official journal of the International Association for the Study of the Liver.

[6]  D. Harnois Prolonged Therapy of Advanced Chronic Hepatitis C with Low-Dose Peginterferon , 2009 .

[7]  William M. Lee,et al.  Prolonged therapy of advanced chronic hepatitis C with low-dose peginterferon. , 2008, The New England journal of medicine.

[8]  K. Neal Excess mortality rates in a cohort of patients infected with the hepatitis C virus: a prospective study , 2007, Gut.

[9]  A. Andriulli,et al.  Peginterferon alfa-2b and ribavirin in patients with hepatitis C virus and decompensated cirrhosis: a controlled study. , 2007, Journal of hepatology.

[10]  J. Hoofnagle,et al.  Mechanism of action of interferon and ribavirin in treatment of hepatitis C , 2005, Nature.

[11]  L. McNutt,et al.  Estimating the mortality rate of hepatitis C using multiple data sources , 2004, Epidemiology and Infection.

[12]  William M. Lee,et al.  Evolution of the HALT-C Trial: pegylated interferon as maintenance therapy for chronic hepatitis C in previous interferon nonresponders. , 2004, Controlled clinical trials.

[13]  A. Alberti,et al.  Natural history of compensated viral cirrhosis: a prospective study on the incidence and hierarchy of major complications , 2004, Gut.

[14]  M. Fried,et al.  Side effects of therapy of hepatitis C and their management , 2002, Hepatology.

[15]  L. Seeff,et al.  Natural history of chronic hepatitis C , 2002, Hepatology.

[16]  Dieter Häussinger,et al.  Peginterferon alfa-2a plus ribavirin for chronic hepatitis C virus infection. , 2002, The New England journal of medicine.

[17]  C. Samuel,et al.  Antiviral Actions of Interferons , 2001, Clinical Microbiology Reviews.

[18]  Kenneth Koury,et al.  For Personal Use. Only Reproduce with Permission from the Lancet Publishing Group , 2022 .

[19]  K. Ishak,et al.  Long‐term mortality and morbidity of transfusion‐associated non‐A, non‐B, and type C hepatitis: A National Heart, Lung, and Blood Institute collaborative study , 2001, Hepatology.

[20]  E. Kenny‐Walsh Clinical outcomes after hepatitis C infection from contaminated anti-D immune globulin. Irish Hepatology Research Group. , 1999, The New England journal of medicine.

[21]  P. Bonis Clinical outcomes after hepatitis C infection from contaminated anti-D immune globulin. , 1999, The New England journal of medicine.

[22]  A. Bhalla,et al.  Morbidity and mortality in compensated cirrhosis type C: a retrospective follow-up study of 384 patients. , 1997, Gastroenterology.

[23]  M. Tong,et al.  Clinical outcomes after transfusion-associated hepatitis C. , 1995, The New England journal of medicine.

[24]  K. Ishak,et al.  Chronic hepatitis: morphology and nomenclature. , 1994, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

[25]  R. Esteban,et al.  Epidemiology of hepatitis C virus infection. , 1993, Journal of hepatology.