Individualized treatment with combination of Peg-interferon alpha 2b and ribavirin in patients infected with HCV genotype 3

被引:20
作者
Mangia, Alessandra [1 ]
Bandiera, Franco [3 ]
Montalto, Giuseppe [4 ]
Mottola, Leonardo [1 ]
Piazzolla, Valeria [1 ]
Minerva, Nicola [5 ]
Pellicelli, Adriano [6 ]
Ricci, Giovanni L. [7 ]
Cela, Marina [8 ]
Carretta, Vito [9 ]
Scotto, Gaetano [10 ]
Bacca, Donato [11 ]
Annicchiarico, Brigida [12 ]
Romano, Mario [13 ]
Russello, Maurizio [14 ]
Barbarini, Giorgio [16 ]
Agostinacchio, Ernesto [15 ]
Andriulli, Angelo [2 ]
机构
[1] Casa Sollievo Sofferenza Hosp, IRCCS, Liver Unit, I-71013 San Giovanni Rotondo, Italy
[2] Casa Sollievo Sofferenza Hosp, IRCCS, Div Gastroenterol, San Giovanni Rotondo, Italy
[3] Internal Med Hosp, Sassari, Italy
[4] Internal Med Univ Palermo, Palermo, Italy
[5] Internal Med Hosp, Canosa, Italy
[6] Gastroenterol Hosp S Camillo, Rome, Italy
[7] Internal Med Univ La Sapienza, Rome, Italy
[8] Gastroenterol Osped Riuniti, Foggia, Italy
[9] Internal Med Hosp, Venosa, Italy
[10] Infect Dis Univ Foggia, Foggia, Italy
[11] Internal Med Hosp, Casarano, Italy
[12] Internal Med Catholic Univ, Rome, Italy
[13] Internal Med Hosp S Pertini, Rome, Italy
[14] Internal Med Hosp G Garibaldi, Catania, Italy
[15] Internal Med Clin Santa Rita, Bari, Italy
[16] Policlin San Matteo, Infect Dis IRCCS, Pavia, Italy
关键词
HCV genotype 3; Ribavirin; Peg interferon; Short treatment; CHRONIC HEPATITIS-C; PLUS RIBAVIRIN; PEGINTERFERON ALPHA-2A; TREATMENT DURATION; ANTIVIRAL THERAPY; TELAPREVIR; MANAGEMENT; STEATOSIS;
D O I
10.1016/j.jhep.2010.04.042
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims The benefit of individualizing treatment for patients with genotype 3 HCV infection on the basis of viral clearance at week 4 (wk4-R) has not been firmly established Methods Four hundred and fourteen patients received Peginterferon alpha-2b plus 1000-1200 mg of ribavirin daily according with body weight > or <75 kg Patients were randomized to standard 24 weeks (Std24) or to a 12 or 36 weeks variable treatment duration (Var12/36) In the variable treatment arm patients with or without wk4-R were allocated to either 12 or 36 weeks duration Results At treatment week 4 HCV RNA was undetectable in 262 patients (63 3%) 136 in the Std24 and 126 in the Van 2/36 group (p = 0 41) In patients with wk4-R end-of-treatment (EOT) responses were 80 4% (Cl 85 4-95 3) and 97 6% (Cl 949-99 9) in the two arms respectively (p = 0 019) In patients without wk4-R, corresponding rates were 61 9% (50 6-73 2) and 75 3% (CI 65 9-846) (p = 0 08) SVR was attained in 302 patients 71 4% (Cl 65 3-77 6) in the St24 group and 743% (CI 58 4-80 3) in the variable 12/36 arm Among patients with wk4-R SVR was 81 6% (Cl 75 1-88 1) and 82 5% (75 9-89 1) respectively In patients without wk4-R SVR amounted to 52 1% (Cl 40 4-63 7) and 61 7 (CI 51 1-72 3) in the two arms (p = 0 25) Conclusions HCV genotype 3 patients with week4-R may be treated safely with 12 weeks of therapy provided that sufficiently high doses of ribavirin are administered For patients still viremic at treatment week 4 SVR rates were numerically higher after 36 weeks of treatment than after the currently recommended 24 weeks (C) 2010 European Association for the Study of the Liver Published by Elsevier B V All rights reserved
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页码:1000 / 1005
页数:6
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