Risk factors for hepatocellular carcinoma at baseline and 1 year after initiation of nucleos(t)ide analog therapy for chronic hepatitis B

Nucleos(t)ide analogs (NAs) cannot completely suppress the risk of hepatocellular carcinoma (HCC) in patients with chronic hepatitis B (CHB). This study aimed to identify the risk factors for HCC development in naïve CHB patients treated with current NA. Patients receiving NA (n = 905) were recruite...

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Veröffentlicht in:Journal of medical virology 2023-01, Vol.95 (1), p.e28210-n/a
Hauptverfasser: Kaneko, Shun, Kurosaki, Masayuki, Mashiba, Toshie, Marusawa, Hiroyuki, Kondo, Masahiko, Kojima, Yuji, Uchida, Yasushi, Fujii, Hideki, Akahane, Takehiro, Yagisawa, Hitoshi, Kusakabe, Atsunori, Kobashi, Haruhiko, Abe, Takehiko, Yoshida, Hideo, Ogawa, Chikara, Furuta, Koichiro, Tamaki, Nobuharu, Tsuji, Keiji, Matsushita, Tomomichi, Izumi, Namiki
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Sprache:eng
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Zusammenfassung:Nucleos(t)ide analogs (NAs) cannot completely suppress the risk of hepatocellular carcinoma (HCC) in patients with chronic hepatitis B (CHB). This study aimed to identify the risk factors for HCC development in naïve CHB patients treated with current NA. Patients receiving NA (n = 905) were recruited retrospectively from the 17 hospitals of the Japanese Red Cross Liver Study Group. All treatment‐naïve patients had been receiving current NA continuously for more than 1 year until the end of the follow‐up. We analyzed the accuracy of predictive risk score using the area under receiver operating characteristic curve. The albumin–bilirubin (ALBI) score was significantly improved by NA therapy (−0.171 ± 0.396; p 
ISSN:0146-6615
1096-9071
DOI:10.1002/jmv.28210