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HEPATOLOGY, VOLUME 62, NUMBER 1 (SUPPL) AASLD ABSTRACTS 727A<br />

Christoph Sarrazin - Advisory Committees or Review Panels: Bristol-Myers<br />

Squibb, Janssen, Merck/MSD, Gilead, Roche, Abbvie, Janssen, Merck/MSD;<br />

Consulting: Merck/MSD, Merck/MSD; Grant/Research Support: Abbott, Roche,<br />

Merck/MSD, Gilead, Janssen, Abbott, Roche, Merck/MSD, Qiagen; Speaking<br />

and Teaching: Gilead, Novartis, Abbott, Roche, Merck/MSD, Janssen, Siemens,<br />

Falk, Abbvie, Bristol-Myers Squibb, Achillion, Abbott, Roche, Merck/MSD, Janssen<br />

The following authors have nothing to disclose: Simone Susser, Christoph P. Berg,<br />

Caterina Berkowski<br />

1056<br />

Hepatocellular carcinoma development in hepatitis C<br />

virus patients who achieved sustained viral response by<br />

interferon therapy: a large scale, long-term cohort study<br />

Yuko Nagaoki, Hiroshi Aikata, Hiromi Kan, Hatsue Fujino, Tomoki<br />

Kobayashi, Takayuki Fukuhara, Keiichi Masaki, Takashi Nakahara,<br />

Tomokazu Kawaoka, Masataka Tsuge, Akira Hiramatu,<br />

Michio Imamura, Yoshiiku Kawakami, Hidenori Ochi, Kazuaki<br />

Chayama; Department of Gastroenterology and Metabolism, Hiroshima<br />

University, Hiroshima, Japan<br />

Background We assessed risk factors for the development of<br />

hepatocellular carcinoma (HCC) following successful eradication<br />

of hepatitis C virus (HCV) with interferon therapy in a longterm,<br />

large-scale cohort study. Methods We reviewed 2262<br />

consecutive patients with HCV infection who achieved sustained<br />

viral response (SVR) by interferon therapy between January<br />

1995 and September 2013 in our study group. Among them,<br />

1094 patients who met the following inclusion criteria were<br />

enrolled in this retrospective cohort study: 1) received HCC<br />

surveillance by tumor markers (AFP, DCP), ultrasonography<br />

and/or dynamic computed tomography at least biannually; 2)<br />

underwent histological examination with liver biopsy before<br />

IFN therapy; and 3) with no evidence of HCC development<br />

prior to HCV eradication and within a year following eradication.<br />

We assessed host, pre-IFN treatment, and post-treatment<br />

risk factors associated with HCC development among these<br />

SVR patients. Results 1) Patients included 585 males aged 11<br />

to 85 years (median 60) at the time of HCV eradication. 581<br />

patients had HCV genotype 1b, and 513 had genotypes 2a,<br />

2b or other genotypes. 936 patients had interferon lambda 3<br />

(IFNL3) SNP rs8099917 genotype TT, and 158 had genotypes<br />

GG or TG. 885 patients had DEPDC5 SNP rs1012068 genotype<br />

TT, and 209 had genotype GG or TG. Histological fibrosis<br />

stage before IFN treatment was as follows: F0 or F1, 492;<br />

F2, 39; F3, 174; and F4, 34. 2) During the observation period<br />

(median 50 months: range 13-224), 36 (3%) of 1094 patients<br />

developed HCC after HCV eradication. The median period<br />

from HCV eradication to HCC development was 37 months<br />

(range 17-141), and the cumulative rates of developing HCC<br />

at 5,10 and 15 years were 4%, 6% and 12%, respectively. 3)<br />

As independent risk factors for HCC development, multivariate<br />

analysis identified older age ≥ 60 years (HR, 3.1: 95%CI,<br />

1.3-6.6: P=0.009), male sex (HR, 11.9: 95%CI, 2.8-50.0:<br />

P

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