論文

査読有り 国際誌
2020年5月6日

Sex difference in the development of hepatocellular carcinoma after direct-acting antiviral therapy in patients with HCV infection.

Journal of medical virology
  • Takao Watanabe
  • Yoshio Tokumoto
  • Kouji Joko
  • Kojiro Michitaka
  • Norio Horiike
  • Yoshinori Tanaka
  • Fujimasa Tada
  • Yoshiyasu Kisaka
  • Seiji Nakanishi
  • Kazuhiko Yamauchi
  • Atsushi Yukimoto
  • Yoshiko Nakamura
  • Masashi Hirooka
  • Masanori Abe
  • Yoichi Hiasa
  • 全て表示

記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1002/jmv.25984

Sex differences in the predictors for hepatocellular carcinoma (HCC) development after direct-acting antiviral (DAA) therapy was investigated. DAA therapy was given to 1438 (663 male, 775 female) patients. Sex differences in the HCC development rate and the factors contributing to HCC development after DAA therapy were investigated. Male patients had a significantly higher cumulative HCC incidence (log-rank test, P =  .007). On multivariate analysis, the fibrosis-4 index (HR = 1.11; 95%CI, 1.042-1.202, P =  .002) and posttreatment α-fetoprotein (AFP) (HR = 1.11; 95%CI, 1.046-1.197, P  =  .001) were found to be independent factors that contributed to HCC development following DAA therapy in female patients, whereas only posttreatment AFP (HR  =  1.090; 95%CI, 1.024-1.160, P  = .007) was an independent factor in male patients. The optimal posttreatment AFP cut-off values were set based on receiver operating characteristic curve analyses. The optimal posttreatment AFP cut-off value was much higher in females (6.0 ng/mL) than in male (3.5 ng/mL) patients. In conclusion both in male and female patients, posttreatment AFP was an independent predictor of HCC development after DAA therapy. However, the cut-off values differed between the sexes. In male patients, HCC could be seen in patients with relatively low posttreatment AFP levels; more careful observation might be needed in such patients.

リンク情報
DOI
https://doi.org/10.1002/jmv.25984
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/32374470
ID情報
  • DOI : 10.1002/jmv.25984
  • PubMed ID : 32374470

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