Maintenance Therapy With Peginterferon Alfa-2b Does Not Prevent Hepatocellular Carcinoma in Cirrhotic Patients With Chronic Hepatitis C

被引:97
作者
Bruix, Jordi [1 ]
Poynard, Thierry
Colombo, Massimo [2 ]
Schiff, Eugene [3 ]
Burak, Kelly [4 ]
Heathcote, Elizabeth J. L. [5 ]
Berg, Thomas [6 ]
Poo, Jorge-Luis [7 ,8 ]
Mello, Carlos Brandao [9 ]
Guenther, Rainer [10 ]
Niederau, Claus [11 ]
Terg, Ruben [12 ]
Bedossa, Pierre [13 ,14 ]
Boparai, Navdeep [15 ]
Griffel, Louis H.
Burroughs, Margaret
Brass, Clifford A.
Albrecht, Janice K.
机构
[1] Univ Barcelona, Hosp Clin Barcelona, Ctr Invest Biomed Red Hepatol & Enfermedades Dige, IDIBAPS,Liver Unit,BCLC Grp, E-08036 Barcelona, Spain
[2] Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Div Gastroenterol 1, Milan, Italy
[3] Univ Miami, Sch Med, Ctr Liver Dis, Miami, FL USA
[4] Univ Calgary, Dept Med, Div Gastroenterol, Liver Unit, Calgary, AB, Canada
[5] Univ Toronto, Toronto Western Hosp, Toronto Western Res Inst, Patient Based Clin Res Div, Toronto, ON M5T 2S8, Canada
[6] Univ Med Berlin, Campus Virchow Klinikum, Charite, Berlin, Germany
[7] Med Sur Hosp, Mexico City, DF, Mexico
[8] Clin Fdn, Mexico City, DF, Mexico
[9] Univ Rio de Janeiro, Sch Med, Gastroenterol & Liver Unit, Gaffree & Guinle Univ Hosp, Rio De Janeiro, Brazil
[10] Univ Klinikum Schleswig Holstein, Klin Allgemeine Innere Med, Kiel, Germany
[11] St Josef Hosp Oberhausen, Oberhausen, Germany
[12] Hosp Municipal Gastroenterol Dr Bonorino Udaondo, Buenos Aires, Argentina
[13] Hop Beaujon, Dept Pathol, Paris, France
[14] Univ Paris 07, Paris, France
[15] Merck Sharp & Dohme Corp, Whitehouse Stn, NJ USA
关键词
Liver Cancer; Evaluation of PegIntron in Control of Hepatitis C Cirrhosis Program; EPIC3; Program; Clinical Trial; INTERFERON THERAPY; VIRUS; TRIAL;
D O I
10.1053/j.gastro.2011.03.010
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: Several studies have reported that low doses of interferon can delay the development of hepatocellular carcinoma (HCC) and progression of chronic hepatitis C. We investigated the incidence of clinical events among participants of the Evaluation of PegIntron in Control of Hepatitis C Cirrhosis (EPIC) 3 program. METHODS: Data were analyzed from an open-label randomized study of patients with chronic hepatitis C who had failed to respond to interferon alfa plus ribavirin. All patients had compensated cirrhosis with no evidence of HCC. Patients received peginterferon alfa-2b (0.5 mu g/kg/week; n = 311) or no treatment (controls, n = 315) for a maximum period of 5 years or until 98 patients had a clinical event (hepatic decompensation, HCC, death, or liver transplantation). The primary measure of efficacy was time until the first clinical event. RESULTS: There was no significant difference in time to first clinical event among patients who received peginterferon alfa-2b compared with controls (hazard ratio [HR], 1.452; 95%confidence interval [CI]: 0.880-2.396). There was no decrease in the development of HCC with therapy. The time to disease progression (clinical events or new or enlarged varices) was significantly longer for patients who received peginterferon alfa-2b compared with controls (HR, 1.564; 95% CI: 1.130-2.166). In a prospectively defined subanalysis of patients with baseline portal hypertension, peginterferon alfa-2b significantly increased the time to first clinical event compared with controls (P=.016). There were no new safety observations. CONCLUSIONS: Maintenance therapy with peginterferon alfa-2b is not warranted in all patients and does not prevent HCC. However, there is a potential clinical benefit of long-term suppressive therapy in patients with preexisting portal hypertension.
引用
收藏
页码:1990 / 1999
页数:10
相关论文
共 24 条
  • [1] AFDHAL N, 2008, 43 ANN M EUR ASS STU, P23
  • [2] [Anonymous], 1998, Lancet, V351, P1535
  • [3] Use of interferon for prevention of hepatocellular carcinoma in cirrhotic patients with hepatitis B or hepatitis B virus infection
    Baffis, V
    Shrier, I
    Sherker, AH
    Szilagyi, A
    [J]. ANNALS OF INTERNAL MEDICINE, 1999, 131 (09) : 696 - 701
  • [4] Management of hepatoceullular carcinoma
    Bruix, J
    Sherman, M
    [J]. HEPATOLOGY, 2005, 42 (05) : 1208 - 1236
  • [5] Sustained Virologic Response Prevents the Development of Esophageal Varices in Compensated, Child-Pugh Class A Hepatitis C Virus-Induced Cirrhosis. A 12-Year Prospective Follow-up Study
    Bruno, Savino
    Crosignani, Andrea
    Facciotto, Corinna
    Rossi, Sonia
    Roffi, Luigi
    Redaelli, Alessandro
    de Franchis, Roberto
    Almasio, Piero Luigi
    Maisonneuve, Patrick
    [J]. HEPATOLOGY, 2010, 51 (06) : 2069 - 2076
  • [6] Evolving consensus in portal hypertension - Report of the Baveno IV Consensus Workshop on methodology of diagnosis and therapy in portal hypertension
    de Franchis, R
    [J]. JOURNAL OF HEPATOLOGY, 2005, 43 (01) : 167 - 176
  • [7] Prolonged Therapy of Advanced Chronic Hepatitis C with Low-Dose Peginterferon
    Di Bisceglie, Adrian M.
    Shiffman, Mitchell L.
    Everson, Gregory T.
    Lindsay, Karen L.
    Everhart, James E.
    Wright, Elizabeth C.
    Lee, William M.
    Lok, Anna S.
    Bonkovsky, Herbert L.
    Morgan, Timothy R.
    Ghany, Marc G.
    Morishima, Chihiro
    Snow, Kristin K.
    Dienstag, Jules L.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2008, 359 (23) : 2429 - 2441
  • [8] Factors That Determine the Development and Progression of Gastroesophageal Varices in Patients With Chronic Hepatitis C
    Fontana, Robert J.
    Sanyal, Arun J.
    Ghany, Marc G.
    Lee, William M.
    Reid, Andrea E.
    Naishadham, Deepa
    Everson, Gregory T.
    Kahn, Jeffrey A.
    Di Bisceglie, Adrian M.
    Szabo, Gyongyi
    Morgan, Timothy R.
    Everhart, James E.
    [J]. GASTROENTEROLOGY, 2010, 138 (07) : 2321 - U176
  • [9] Long-term interferon therapy for 1 year or longer reduces the hepatocellular carcinogenesis rate in patients with liver cirrhosis caused by hepatitis C virus: A pilot study
    Ikeda, K
    Saitoh, S
    Kobayashi, M
    Suzuki, Y
    Suzuki, F
    Tsubota, A
    Arase, Y
    Murashima, N
    Chayama, K
    Kumada, H
    [J]. JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2001, 16 (04) : 406 - 415
  • [10] *INT C HARM EXP WO, 1996, E6R1 INT C HARM EXP, P1