Predictive value of the IFNL4 polymorphism on outcome of telaprevir, peginterferon, and ribavirin therapy for older patients with genotype 1b chronic hepatitis C

被引:15
作者
Fujino, Hatsue [1 ]
Imamura, Michio [1 ]
Nagaoki, Yuko [1 ]
Kawakami, Yoshiiku [1 ]
Abe, Hiromi [1 ]
Hayes, C. Nelson [1 ]
Kan, Hiromi [1 ]
Fukuhara, Takayuki [1 ]
Kobayashi, Tomoki [1 ]
Masaki, Keiichi [1 ]
Ono, Atsushi [1 ]
Nakahara, Takashi [1 ]
Honda, Youji
Naeshiro, Noriaki [1 ]
Urabe, Ayako [1 ]
Yokoyama, Satoe
Miyaki, Daisuke [1 ]
Murakami, Eisuke [1 ]
Kawaoka, Tomokazu [1 ]
Hiraga, Nobuhiko [1 ]
Tsuge, Masataka [1 ]
Hiramatsu, Akira [1 ]
Hyogo, Hideyuki [1 ]
Aikata, Hiroshi [1 ]
Takahashi, Shoichi [1 ]
Miki, Daiki [2 ]
Ochi, Hidenori [2 ]
Ohishi, Waka [3 ]
Chayama, Kazuaki [1 ,2 ]
机构
[1] Hiroshima Univ, Dept Gastroenterol & Metab, Appl Life Sci, Inst Biomed & Hlth Sci,Minami Ku, Hiroshima 7348551, Japan
[2] Inst Phys & Chem Res RIKEN, Lab Digest Dis, Ctr Genom Med, Hiroshima, Japan
[3] Radiat Effects Res Fdn, Dept Clin Studies, Hiroshima, Japan
关键词
Hepatitis C virus; Telaprevir; Older patients; IFNL4; RVR; PEGYLATED INTERFERON; COMBINATION THERAPY; PLUS RIBAVIRIN; GENOME-WIDE; HEPATOCELLULAR-CARCINOMA; ITPA POLYMORPHISM; GENETIC-VARIATION; VIRAL RESPONSE; CORE REGION; VIRUS;
D O I
10.1007/s00535-013-0924-9
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Older patients with chronic hepatitis C have a lower virological response to interferon (IFN) treatment compared to younger patients. The efficacy of telaprevir (TVR) and PEG-IFN plus ribavirin combination therapy and the predictive value of recently identified IFN lambda (IFNL) 4 polymorphisms on the outcome of therapy for older patients have not been addressed. We assessed predictive factors for sustained virological response (SVR) to triple therapy in 226 younger (a parts per thousand currency sign65 years) and 87 older (> 65 years) Japanese patients with chronic genotype 1 hepatitis C. IFNL4 polymorphism ss469415590 was analyzed by Invader assay. The SVR rate for older patients was slightly lower than for younger patients (69 vs. 82 %, P = 0.043). In the older group, the SVR rate for patients with the IFNL4 TT/TT genotype was significantly higher than patients with TT/Delta G or Delta G/Delta G genotypes (81.8 and 42.9 %, P = 0.003). In multivariate regression analysis, rapid virological response (OR 36.601, P = 0.002) and IFNL4 TT/TT genotype (OR 19.502, P = 0.009) were identified as significant independent predictors for SVR in older patients. Treatment-related decreases in hemoglobin and increases in serum creatinine were higher in older patients than younger patients. Reduction of initial TVR dose to 1,500 mg per day alleviated these adverse events without compromising SVR rate in older patients. Analysis of IFNL4 polymorphisms is a valuable predictor in older patients receiving TVR triple therapy. 1,500 mg per day is a suitable initial TVR dose for older Japanese patients.
引用
收藏
页码:1548 / 1556
页数:9
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