Excess Mortality in Patients with Advanced Chronic Hepatitis C Treated with Long-Term Peginterferon

被引:51
作者
Di Bisceglie, Adrian M. [1 ]
Stoddard, Anne M. [2 ]
Dienstag, Jules L. [3 ,4 ]
Shiffman, Mitchell L. [5 ]
Seeff, Leonard B. [6 ,7 ]
Bonkovsky, Herbert L. [8 ,9 ]
Morishima, Chihiro [10 ]
Wright, Elizabeth C. [11 ]
Snow, Kristin K. [2 ]
Lee, William M. [12 ]
Fontana, Robert J. [13 ]
Morgan, Timothy R. [14 ,15 ]
Ghany, Marc G. [7 ]
机构
[1] St Louis Univ, Sch Med, Dept Internal Med, Div Gastroenterol & Hepatol, St Louis, MO 63104 USA
[2] New England Res Inst, Watertown, MA 02172 USA
[3] Massachusetts Gen Hosp, Gastrointestinal Unit, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[5] Bon Secours Hlth Syst, Liver Inst Virginia, Newport News, VA USA
[6] NIDDKD, Div Digest Dis & Nutr, NIH, Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[7] NIDDKD, Liver Dis Branch, NIH, Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[8] Univ Connecticut, Ctr Hlth, Dept Med, Farmington, CT USA
[9] Carolinas Med Ctr, Charlotte, NC 28203 USA
[10] Univ Washington, Dept Lab Med, Div Virol, Seattle, WA 98195 USA
[11] NIDDKD, Off Director, NIH, Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[12] Univ Texas SW Med Ctr Dallas, Div Digest & Liver Dis, Dallas, TX 75390 USA
[13] Univ Michigan, Sch Med, Dept Internal Med, Div Gastroenterol, Ann Arbor, MI USA
[14] Univ Calif Irvine, Div Gastroenterol, Irvine, CA USA
[15] VA Long Beach Healthcare Syst, Gastroenterol Serv, Long Beach, CA USA
基金
美国国家卫生研究院;
关键词
COMPENSATED CIRRHOSIS; CLINICAL-OUTCOMES; NATURAL-HISTORY; VIRUS-INFECTION; PLUS RIBAVIRIN; THERAPY; INTERFERON; MANAGEMENT; MORBIDITY; ALPHA-2B;
D O I
10.1002/hep.24169
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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;53:1100-1108)
引用
收藏
页码:1100 / 1108
页数:9
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