Favorable efficacy of daclatasvir plus asunaprevir in treatment of elderly Japanese patients infected with HCV genotype 1b aged 70 and older

被引:28
作者
Akuta, Norio [1 ]
Sezaki, Hitomi [1 ]
Suzuki, Fumitaka [1 ]
Kawamura, Yusuke [1 ]
Hosaka, Tetsuya [1 ]
Kobayashi, Masahiro [1 ]
Kobayashi, Mariko [2 ]
Saitoh, Satoshi [1 ]
Suzuki, Yoshiyuki [1 ]
Arase, Yasuji [1 ]
Ikeda, Kenji [1 ]
Kumada, Hiromitsu [1 ]
机构
[1] Toranomon Gen Hosp, Dept Hepatol, Okinaka Mem Inst Med Res, Tokyo, Japan
[2] Toranomon Gen Hosp, Liver Res Lab, Tokyo, Japan
关键词
HCV; daclatasvir; asunaprevir; elderly; AFP; liver stiffness; resistance-associated variant; NS3; NS5A; HEPATITIS-C; HEPATOCELLULAR-CARCINOMA; PROTEASE INHIBITOR; THERAPY;
D O I
10.1002/jmv.24592
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The combination of daclatasvir and asunaprevir is efficacious in the treatment of hepatitis C virus (HCV) infection, but its efficacy and predictors of efficacy in the elderly (70 years) remain unclear. In this study, 844 patients with chronic HCV genotype 1b infection, were treated with daclatasvir (60mg once daily) plus asunaprevir (100mg twice daily) for 24 weeks. Using the intention-to-treat analysis, the sustained virological response (SVR) rates were 87% and 88% for all 844 patients and 411 elderly (>70 years of age), respectively. In both groups, multivariate analysis identified NS5A-Y93H mutation (<20%), pretreatment (failure of treatment except for triple therapy with simeprevir, or treatment naive), and level of viremia (<6.0 log IU/ml) as independent predictors of SVR. Direct sequencing showed a significantly higher rate of NS3-D168 mutation at baseline in non-responders to triple therapy with simeprevir (44%) than others (2%). Alfa-fetoprotein (AFP) level and liver stiffness were significantly lower after end of treatment than at baseline, in both the SVR and non-SVR groups. In conclusion, daclatasvir-asunaprevir combination achieved high SVR in HCV genotype 1b patients, including elderly patients. Viral factors negatively influenced the response to treatment. Treatment improved AFP level and liver stiffness (surrogate markers of hepatocellular carcinoma), regardless of treatment efficacy. J. Med. Virol. 89:91-98, 2017. (c) 2016 Wiley Periodicals, Inc.
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页码:91 / 98
页数:8
相关论文
共 21 条
[1]   Substitution of amino acid 70 in the hepatitis C virus core region of genotype 1b is an important predictor of elevated alpha-fetoprotein in patients without hepatocellular carcinoma [J].
Akuta, Norio ;
Suzuki, Fumitaka ;
Kawamura, Yusuke ;
Yatsuji, Hiromi ;
Sezaki, Hitomi ;
Suzuki, Yoshiyuki ;
Hosaka, Tetsuya ;
Kobayashi, Masahiro ;
Kobayashi, Mariko ;
Arase, Yasuji ;
Ikeda, Kenji ;
Kumada, Hiromitsu .
JOURNAL OF MEDICAL VIROLOGY, 2008, 80 (08) :1354-1362
[2]   Determination of reliability criteria for liver stiffness evaluation by transient elastography [J].
Boursier, Jerome ;
Zarski, Jean-Pierre ;
de Ledinghen, Victor ;
Rousselet, Marie-Christine ;
Sturm, Nathalie ;
Lebail, Brigitte ;
Fouchard-Hubert, Isabelle ;
Gallois, Yves ;
Oberti, Frederic ;
Bertrais, Sandrine ;
Cales, Paul .
HEPATOLOGY, 2013, 57 (03) :1182-1191
[3]   Dual therapy with the nonstructural protein 5A inhibitor, daclatasvir, and the nonstructural protein 3 protease inhibitor, asunaprevir, in hepatitis C virus genotype 1b-infected null responders [J].
Chayama, Kazuaki ;
Takahashi, Shoichi ;
Toyota, Joji ;
Karino, Yoshiyasu ;
Ikeda, Kenji ;
Ishikawa, Hiroki ;
Watanabe, Hideaki ;
McPhee, Fiona ;
Hughes, Eric ;
Kumada, Hiromitsu .
HEPATOLOGY, 2012, 55 (03) :742-748
[4]   Projecting future complications of chronic hepatitis C in the United States [J].
Davis, GL ;
Albright, JE ;
Cook, SF ;
Rosenberg, DM .
LIVER TRANSPLANTATION, 2003, 9 (04) :331-338
[5]   Antiviral activity and resistance of HCV NS5A replication complex inhibitors [J].
Gao, Min .
CURRENT OPINION IN VIROLOGY, 2013, 3 (05) :514-520
[6]  
Kan H., 2015, ANTIVIR THER
[7]   Characterization of virologic escape in hepatitis C virus genotype 1b patients treated with the direct-acting antivirals daclatasvir and asunaprevir [J].
Karino, Yoshiyasu ;
Toyota, Joji ;
Ikeda, Kenji ;
Suzuki, Fumitaka ;
Chayama, Kazuaki ;
Kawakami, Yoshiiku ;
Ishikawa, Hiroki ;
Watanabe, Hideaki ;
Hernandez, Dennis ;
Yu, Fei ;
McPhee, Fiona ;
Kumada, Hiromitsu .
JOURNAL OF HEPATOLOGY, 2013, 58 (04) :646-654
[8]   Daclatasvir Plus Asunaprevir for Chronic HCV Genotype 1b Infection [J].
Kumada, Hiromitsu ;
Suzuki, Yoshiyuki ;
Ikeda, Kenji ;
Toyota, Joji ;
Karino, Yoshiyasu ;
Chayama, Kazuaki ;
Kawakami, Yoshiiku ;
Ido, Akio ;
Yamamoto, Kazuhide ;
Takaguchi, Koichi ;
Izumi, Namiki ;
Koike, Kazuhiko ;
Takehara, Tetsuo ;
Kawada, Norifumi ;
Sata, Michio ;
Miyagoshi, Hidetaka ;
Eley, Timothy ;
McPhee, Fiona ;
Damokosh, Andrew ;
Ishikawa, Hiroki ;
Hughes, Eric .
HEPATOLOGY, 2014, 59 (06) :2083-2091
[9]   Appropriate use of virtual touch quantification and FibroScanA® M and XL probes according to the skin capsular distance [J].
Kumagai, Erina ;
Korenaga, Keiko ;
Korenaga, Masaaki ;
Imamura, Masatoshi ;
Ueyama, Misuzu ;
Aoki, Yoshihiko ;
Sugiyama, Masaya ;
Murata, Kazumoto ;
Masaki, Naohiko ;
Kanto, Tatsuya ;
Mizokami, Masashi ;
Watanabe, Sumio .
JOURNAL OF GASTROENTEROLOGY, 2016, 51 (05) :496-505
[10]   Preliminary Study of Two Antiviral Agents for Hepatitis C Genotype 1 [J].
Lok, Anna S. ;
Gardiner, David F. ;
Lawitz, Eric ;
Martorell, Claudia ;
Everson, Gregory T. ;
Ghalib, Reem ;
Reindollar, Robert ;
Rustgi, Vinod ;
McPhee, Fiona ;
Wind-Rotolo, Megan ;
Persson, Anna ;
Zhu, Kurt ;
Dimitrova, Dessislava I. ;
Eley, Timothy ;
Guo, Tong ;
Grasela, Dennis M. ;
Pasquinelli, Claudio .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (03) :216-224