DOI: 10.1111/hepr.13955 ISSN:

Artificial intelligence/neural network system that accurately diagnoses hepatocellular carcinoma in nonalcoholic steatohepatitis

Takeshi Okanoue, Kanji Yamaguchi, Toshihide Shima, Yasuhide Mitsumoto, Takayuki Katayama, Keiichiro Okuda, Masayuki Mizuno, Yuya Seko, Michihisa Moriguchi, Yoshito Itoh, Toru Miyazaki
  • Infectious Diseases
  • Hepatology

Abstract

Background and Aim

The aim of this study was to develop a novel noninvasive test using an artificial intelligence/neural network system (called HCC‐Scope) to diagnose early‐stage hepatocellular carcinoma (HCC) on the background of nonalcoholic steatohepatitis (NASH).

Methods

One hundred and seventy‐five patients with histologically proven nonalcoholic fatty liver disease and 55 patients with NASH‐HCC were enrolled for training and validation studies. Of the 55 patients with NASH‐HCC, 27 (49.1%) had very early‐stage HCC, and six (10.9%) had early‐stage HCC based on the Barcelona Clinic Liver Cancer staging system. Diagnosis with HCC‐Scope was performed based on 12 items: age, sex, height, weight, aspartate aminotransferase level, alanine aminotransferase level, gamma‐glutamyl transferase level, cholesterol level, triglyceride level, platelet count, diabetes status, and immunoglobulim M‐free apoptosis inhibitor of macrophage level. The FMVWG2U47 hardware (Fujitsu Co. Ltd, Tokyo, Japan) and the originally developed software were used.

Results

HCC‐Scope had sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of 100.0% for differential diagnosis between non‐HCC and HCC in a training study with gray zone analysis. It was also excellent in the validation study (95.0% sensitivity, 100.0% specificity, 100.0% PPV, and 97.1% NPV with gray zone analysis and 95.2% sensitivity, 100.0% specificity, 100.0% PPV, and 97.1% NPV without gray zone analysis). HCC‐Scope had significantly higher sensitivity (85.3%) and specificity (85.1%) than alpha‐fetoprotein (AFP) level, AFP‐L3 level, des‐gamma‐carboxy prothrombin (DCP) level, and the gender–age–AFP‐L3–AFP–DCP (GALAD) score.

Conclusions

HCC‐Scope can accurately differentially diagnose between non‐HCC NASH and NASH‐HCC, including very early‐stage NASH‐HCC.

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