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Predictors of Response to 24-Week Telaprevir-Based Triple Therapy for Treatment-Naïve Genotype 1b Chronic Hepatitis C Patients
Author(s) -
Hiroshi Abe,
Akihito Tsubota,
Noritomo Shimada,
Masanori Atsukawa,
Keizo Kato,
Koichi Takaguchi,
Toru Asano,
Yoshimichi Chuganji,
Choitsu Sakamoto,
Hidenori Toyoda,
Takashi Kumada,
Tatsuya Ide,
Michio Sata,
Yoshio Aizawa
Publication year - 2014
Publication title -
gastroenterology research and practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.622
H-Index - 45
eISSN - 1687-630X
pISSN - 1687-6121
DOI - 10.1155/2014/549709
Subject(s) - telaprevir , medicine , ribavirin , gastroenterology , genotype , logistic regression , hepatitis c virus , adverse effect , chronic hepatitis , virology , virus , biochemistry , chemistry , gene
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-naïve hepatitis C virus (HCV) genotype 1b (G1b) patients. This multicenter study involved 150 Asian treatment-naïve patients infected with HCV G1b who received 12 weeks of telaprevir in combination with 24 weeks of peginterferon- α -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 × 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 × 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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