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Risk of hepatocellular carcinoma in cirrhotic hepatitis B virus patients during nucleoside/nucleotide analog therapy
Author(s) -
Orito Etsuro,
Hasebe Chitomi,
Kurosaki Masayuki,
Osaki Yukio,
Joko Kouji,
Watanabe Hiroshi,
Kimura Hiroyuki,
Nishijima Norihiro,
Kusakabe Atsunori,
Izumi Namiki
Publication year - 2015
Publication title -
hepatology research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.123
H-Index - 75
eISSN - 1872-034X
pISSN - 1386-6346
DOI - 10.1111/hepr.12427
Subject(s) - hepatocellular carcinoma , medicine , hbsag , gastroenterology , cirrhosis , hepatitis b virus , nucleoside analogue , seroconversion , hepatitis b , virus , immunology , nucleoside , biology , biochemistry
Aim Some patients develop hepatocellular carcinoma ( HCC ) during nucleoside/nucleotide analog ( NA ) therapy even if alanine aminotransferase ( ALT ) or hepatitis B virus ( HBV ) DNA levels are sufficiently reduced. The aim of this study is to identify the risk factors of development of HCC during NA therapy. Methods Six hundred and two patients were analyzed who were continuously receiving NA for chronic HBV infection. The patients who developed HCC previously or within 1 year of therapy were excluded. In the patients studied, the median duration of therapy was 90 months. A total of 492 patients had chronic hepatitis ( CH ) and 110 had liver cirrhosis ( LC ). Results In 602 patients, the rate of normalization of ALT , loss of serum HBV DNA and development of HCC were 90.4%, 55.4%, and 6.1%, respectively. The significant risk factors of development of HCC were LC status and duration of therapy. The annual incidence of HCC in LC patients was 2.53%/year, compared with 0.34%/year in CH patients. When the relation between the incidence of HCC and the response to therapy was evaluated, in patients with normalization of ALT level, loss of HBV DNA by real‐time polymerase chain reaction or hepatitis B e‐antigen seroconversion, the incidences of HCC was reduced to some extent. However, none of the patients who achieved hepatitis B surface antigen ( HBsAg ) seroclearance during NA therapy developed HCC . Conclusion LC status was the significant risk factor of development of HCC during NA therapy. However, none of the patients who showed HBsAg seroclearance developed HCC . The ultimate goal of therapy for reduced risk of HCC may be HBsAg seroclearance.