A randomized trial of pegylated interferon α-2b plus ribavirin in the retreatment of chronic hepatitis C

被引:94
作者
Jacobson, IM
Gonzalez, SA
Ahmed, F
Lebovics, E
Min, AD
Bodenheimer, HC
Esposito, SP
Brown, RS
Bräu, N
Klion, FM
Tobias, H
Bini, EJ
Brodsky, N
Cerulli, MA
Aytaman, A
Gardner, PW
Geders, JM
Spivack, JE
Rahmin, MG
Berman, DH
Ehrlich, J
Russo, MW
Chait, M
Rovner, D
Edlin, BR
机构
[1] Cornell Univ, Weill Med Coll, Div Gastroenterol & Hepatol, New York, NY 10021 USA
[2] Cornell Univ, Weill Med Coll, Ctr Study Hepatitis C, New York, NY 10021 USA
[3] New York Med Coll, Div Gastroenterol & Hepatobiliary Dis, Valhalla, NY 10595 USA
[4] Beth Israel Deaconess Med Ctr, Div Digest Dis, New York, NY 10003 USA
[5] Hepatobiliary Associates New York, Bayside, NY USA
[6] Columbia Univ, Coll Phys & Surg, Ctr Liver Dis & Transplantat, New York, NY USA
[7] Columbia Univ, Coll Phys & Surg, Div Digest & Liver Dis, New York, NY USA
[8] Bronx Vet Adm Med Ctr, Div Infect Dis, Bronx, NY USA
[9] Mt Sinai Sch Med, Div Liver Dis, New York, NY USA
[10] NYU, Sch Med, Div Gastroenterol, New York, NY USA
[11] New York VA Med Ctr, Div Gastroenterol & Hepatol, New York, NY USA
[12] Palmadessa & Kuan Gastroenterol Associates, Flushing, NY USA
[13] Brooklyn Hosp Ctr, Div Gastroenterol & Hepatol, Brooklyn, NY USA
[14] VA New York Harbor Healthcare Syst, Div Gastroenterol, Brooklyn, NY USA
[15] Gastroenterol Consultants, Stamford, CT USA
[16] New York Methodist Hosp, Div Gastroenterol & Hepatol, Brooklyn, NY USA
[17] Gastroenterol Associates Fairfield Cty, Fairfield, CT USA
[18] Gastrointestinal Associates, Ridgewood, NJ USA
[19] Pk Ave Med & Gastroenterol, New York, NY USA
[20] Gastroenterol Westchester, Bronxville, NY USA
[21] Hartsdale Med Grp, Hartsdale, NY USA
关键词
D O I
10.1111/j.1572-0241.2005.00282.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: The efficacy of combination therapy with pegylated interferon (PEG IFN) alpha plus ribavirin (RBV) in the retreatment of chronic hepatitis C (CHC) in patients who previously failed combination standard IFN plus RBV or IFN monotherapy has not been well established. METHODS: Three hundred and twenty-one CHC patients including virologic nonresponders to combination IFN plus RBV (n = 219) or IFN monotherapy (n = 47), and relapsers to combination therapy (n = 55) were randomized to receive PEG IFN alpha-2b 1.5 mu g/kg per wk plus RBV 800 mg per day (Regimen A, n = 160) or PEG IFN alpha-2b 1.0 mu g/kg per wk plus RBV 1,000-1,200 mg per day (Regimen B, n = 161) for 48 wks. RESULTS: Sustained virologic response (SVR) occurred in 16% of the overall study population (Regimen A vs B, 18%vs 13%, p= 0.21), in 8% of the combination therapy nonresponders (10%vs 6%, p= 0.35), in 21% of the IFN monotherapy nonresponders (16%vs 27%, p= 0.35), and in 42% of the combination therapy relapsers (50%vs 32%, p= 0.18). In nonresponders to prior combination therapy, HCV ribonucleic acid levels < 100,000 copies/mL at the end of the prior treatment course were associated with an increased SVR compared with levels >= 100,000 copies/mL (21%vs 5%, p= 0.002). In the overall study population, genotype 1 patients had lower SVR rates than others (14%vs 33%, p= 0.01), and African Americans had lower SVR than Caucasians (4%vs 18%, p= 0.01). CONCLUSION: Combination therapy with PEG IFN alpha-2b plus RBV is more effective in patients who relapsed after combination standard IFN plus RBV than in nonresponders to either combination therapy or IFN monotherapy. There was no significant effect of dosing regimen.
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页码:2453 / 2462
页数:10
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