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
引用
收藏
页码:1000 / 1005
页数:6
相关论文
共 50 条
  • [31] Retreatment with peg-interferon and ribavirin in patients with chronic hepatitis C virus genotype 2 or 3 infection with prior relapse
    Lagging, Martin
    Rembeck, Karolina
    Buhl, Mads Rauning
    Christensen, Peer
    Dalgard, Olav
    Farkkila, Martti
    Hellstrand, Kristoffer
    Langeland, Nina
    Lindh, Magnus
    Westin, Johan
    Norkrans, Gunnar
    SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2013, 48 (07) : 839 - 847
  • [32] Influence of HCV Genotype 1 Subtypes on the Virus Response to PEG Interferon Alpha-2a Plus Ribavirin Therapy
    Nicot, F.
    Alric, L.
    Barange, K.
    Metivier, S.
    Dramard, J. M.
    Combis, J. M.
    Castan, B.
    Meurisse, J. J.
    Payen, J. L.
    Garipuy, D.
    Desmorat, H.
    Peron, J. M.
    Thebault, S.
    Morin, T.
    Renou, C.
    Barel, P.
    Guerin, B.
    Imbert, Y.
    Sire, S.
    Saune, K.
    Chatelut, E.
    Izopet, J.
    JOURNAL OF MEDICAL VIROLOGY, 2011, 83 (03) : 437 - 444
  • [33] Lead-in treatment with interferon-β/ribavirin may modify the early hepatitis C virus dynamics in pegylated interferon alpha-2b/ribavirin combination for chronic hepatitis C patients with the IL28B minor genotype
    Itokawa, Norio
    Atsukawa, Masanori
    Tsubota, Akihito
    Kondo, Chisa
    Hashimoto, Satomi
    Fukuda, Takeshi
    Matsushita, Yoko
    Kidokoro, Hideko
    Kobayashi, Tamaki
    Narahara, Yoshiyuki
    Nakatsuka, Katsuhisa
    Kanazawa, Hidenori
    Iwakiri, Katsuhiko
    Sakamoto, Choitsu
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2013, 28 (03) : 443 - 449
  • [34] Combination therapy with interferon-α 2b and ribavirin for the treatment of relapse patients and non-responders with chronic HCV infection
    Kallinowski, B
    Liehr, H
    Moeller, B
    Stremmel, W
    Wechsler, JG
    Wiese, M
    Goeser, T
    ZEITSCHRIFT FUR GASTROENTEROLOGIE, 2001, 39 (03): : 199 - +
  • [35] Effects of ITPA polymorphism on decrease of hemoglobin during simeprevir, peg-interferon, and ribavirin combination treatment for chronic hepatitis C
    Morio, Kei
    Imamura, Michio
    Kawakami, Yoshiiku
    Morio, Reona
    Hatooka, Masahiro
    Kan, Hiromi
    Fujino, Hatsue
    Fukuhara, Takayuki
    Kobayashi, Tomoki
    Masaki, Keiichi
    Ono, Atsushi
    Nakahara, Takashi
    Urabe, Ayako
    Yokoyama, Satoe
    Nagaoki, Yuko
    Kawaoka, Tomokazu
    Hiraga, Nobuhiko
    Tsuge, Masataka
    Hiramatsu, Akira
    Hayes, C. Nelson
    Aikata, Hiroshi
    Ochi, Hidenori
    Chayama, Kazuaki
    HEPATOLOGY RESEARCH, 2016, 46 (12) : 1256 - 1263
  • [36] Combination of fluvastatin with pegylated interferon/ribavirin therapy reduces viral relapse in chronic hepatitis C infected with HCV genotype 1b
    Atsukawa, Masanori
    Tsubota, Akihito
    Kondo, Chisa
    Itokawa, Norio
    Narahara, Yoshiyuki
    Nakatsuka, Katsuhisa
    Hashimoto, Satomi
    Fukuda, Takeshi
    Matsushita, Yoko
    Kidokoro, Hideko
    Kobayashi, Tamaki
    Kanazawa, Hidenori
    Sakamoto, Choitsu
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2013, 28 (01) : 51 - 56
  • [37] Treatment of hepatitis C virus with peg-interferon and ribavirin combination therapy significantly affects lipid metabolism
    Tada, Shinichiro
    Saito, Hidetsugu
    Ebinuma, Hirotoshi
    Ojiro, Keisuke
    Yamagishi, Yoshiyuki
    Kumagai, Naoki
    Inagaki, Yasutaka
    Masuda, Tetsuya
    Nishida, Jiro
    Takahashi, Masahiko
    Nagata, Hiroshi
    Hibi, Toshifumi
    HEPATOLOGY RESEARCH, 2009, 39 (02) : 195 - 199
  • [38] High ability to predict the treatment outcome of peginterferon and ribavirin combination therapy based on the reduction in HCV RNA levels at 4 weeks after starting therapy and amino acid substitutions in the hepatitis C virus in patients infected with HCV genotype 1b
    Toyoda, Hidenori
    Kumada, Takashi
    Kiriyama, Seiki
    Tanikawa, Makoto
    Hisanaga, Yasuhiro
    Kanamori, Akira
    Tada, Toshifumi
    Arakawa, Takahiro
    Fujimori, Masashi
    Niinomi, Takuro
    Ando, Naoto
    Yasuda, Satoshi
    Sakai, Keisuke
    Kimura, Jun
    JOURNAL OF GASTROENTEROLOGY, 2011, 46 (04) : 501 - 509
  • [39] Significance of a reduction in HCV RNA levels at 4 and 12 weeks in patients infected with HCV genotype 1b for the prediction of the outcome of combination therapy with peginterferon and ribavirin
    Toyoda, Hidenori
    Kumada, Takashi
    Shimada, Noritomo
    Takaguchi, Koichi
    Ide, Tatsuya
    Sata, Michio
    Ginba, Hiroyuki
    Matsuyama, Kazuhiro
    Izumi, Namiki
    BMC INFECTIOUS DISEASES, 2012, 12
  • [40] Steatosis is the predictor of relapse in HCV genotype 3- but not 2-infected patients treated with 12 weeks of pegylated interferon-α-2a plus ribavirin and RVR
    Restivo, L.
    Zampino, R.
    Guerrera, B.
    Ruggiero, L.
    Adinolfi, L. E.
    JOURNAL OF VIRAL HEPATITIS, 2012, 19 (05) : 346 - 352