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Predictors of Response to 24-Week Telaprevir-Based Triple Therapy for Treatment-Naive Genotype 1b Chronic Hepatitis C Patients
被引:1
|作者:
Abe, Hiroshi
[1
]
Tsubota, Akihito
[2
]
Shimada, Noritomo
[3
]
Atsukawa, Masanori
[4
]
Kato, Keizo
[3
]
Takaguchi, Koichi
[5
]
Asano, Toru
[6
]
Chuganji, Yoshimichi
[6
]
Sakamoto, Choitsu
[7
]
Toyoda, Hidenori
[8
]
Kumada, Takashi
[8
]
Ide, Tatsuya
[9
]
Sata, Michio
[9
]
Aizawa, Yoshio
[1
]
机构:
[1] Jikei Univ, Sch Med, Katsushika Med Ctr, Dept Internal Med,Div Gastroenterol & Hepatol,Kat, Tokyo 1250062, Japan
[2] Jikei Univ, Sch Med, Inst Clin Med & Res, Kashiwa, Chiba, Japan
[3] Shinmatsudo Cent Gen Hosp, Dept Gastroenterol & Hepatol, Matsudo, Chiba, Japan
[4] Chiba Hokusoh Hosp, Nippon Med Sch, Dept Internal Med, Div Gastroenterol, Inzai, Chiba, Japan
[5] Kagawa Prefectural Cent Hosp, Dept Hepatol, Takamatsu, Kagawa, Japan
[6] Tokyo Metropolitan Bokutoh Hosp, Dept Gastroenterol, Sumida Ku, Tokyo, Japan
[7] Nippon Med Sch, Grad Sch Med, Dept Gastroenterol, Tokyo 113, Japan
[8] Ogaki Municipal Hosp, Dept Gastroenterol, Ogaki, Gifu, Japan
[9] Kurume Univ, Sch Med, Dept Med, Div Gastroenterol, Kurume, Fukuoka 830, Japan
关键词:
AMINO-ACID SUBSTITUTION;
PLUS RIBAVIRIN;
PEGINTERFERON ALPHA-2B;
PEGYLATED INTERFERON;
ANTIVIRAL THERAPY;
GENETIC-VARIATION;
HCV;
IL28B;
ASSOCIATION;
RETREATMENT;
D O I:
10.1155/2014/549709
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
We evaluated the genetic variation in rs8099917, substitutions in core amino acid (aa) 70, and the number of aa substitutions in the interferon sensitivity-determining region (ISDR) on the prediction of sustained virological response (SVR) in treatment-naive hepatitis C virus (HCV) genotype 1b (G1b) patients. This multicenter study involved 150 Asian treatment-naive patients infected with HCV G1b who received 12 weeks of telaprevir in combination with 24 weeks of peginterferon-alpha-2b and ribavirin. The baseline and treatment-related factors potentially associated with SVR were determined by multivariate logistic regression analysis. Virological response was analyzed on an intent-to-treat basis. Cessation of the therapy due to adverse effects occurred in only 2 patients, who discontinued the trial at 10 weeks and at 2 weeks due to cerebral infarction and renal impairment, respectively. Among the 150 patients in whom the final virological response was determined, only genotype TT in rs8099917 was identified as a pretreatment predictor (P = 7.38 x 10(-4)). Achievement of a rapid virological response (RVR), defined as undetectable HCV RNA at week 4 of treatment, was identified as an after-starting-treatment predictor (P = 2.47 x 10(-5)). However, neither a substitution in core aa 70 nor the number of substitutions in the ISDR affected treatment outcome.
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页数:12
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