4.7 Article

Macrotrabecular-massive hepatocellular carcinoma: imaging identification and prediction based on gadoxetic acid-enhanced magnetic resonance imaging

Journal

EUROPEAN RADIOLOGY
Volume 31, Issue 10, Pages 7696-7704

Publisher

SPRINGER
DOI: 10.1007/s00330-021-07898-7

Keywords

Carcinoma; hepatocellular; Magnetic resonance imaging; Nomogram

Funding

  1. National Nature Science Foundation of China [81771797]
  2. Science and Technology Support Program of Sichuan Province [2017SZ0003]

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Necrosis or severe ischemia was found to be a sensitive imaging feature of MTM-HCC, with a high specificity. The combination of specific findings allowed for noninvasive prediction of this subtype with good accuracy and excellent specificity.
Objectives To identify image features of macrotrabecular-massive (MTM) hepatocellular carcinoma (HCC) and to determine its role in predicting MTM-HCC. Methods Patients who underwent preoperative gadoxetic acid-enhanced MRI and with surgery proven HCC were retrospectively included. Imaging features were assessed according to Liver Imaging Reporting and Data System. Quantitative measurements were recorded. Clinical characteristics and imaging findings were compared between MTM-HCCs and non-MTM-HCCs. Predictive factors of MTM-HCC were screened with univariate analyses and then identified with multivariate logistic regression. A regression-based diagnostic model was constructed. ROC analyses were used to determine cutoff values, AUC, and corresponding 95% confidence interval (CI) of findings. The diagnostic performance was validated by 10-fold cross-validation. Results One hundred and forty-one patients with 37 MTM-HCCs were included. Multivariate analyses identified high platelet count (>= 163.5 x 10(3)/ul, odds ratio = 3.20; 95% CI: 1.29, 7.96; p = 0.012), low tumor-to-liver ADC ratio (<= 1.05, odds ratio = 3.05; 95% CI, 1.23 - 7.55; p = 0.016), and necrosis or severe ischemia (odds ratio = 11.61; 95% CI, 3.99 - 33.76, p < 0.001) as independent predictors of MTM-HCC. Necrosis or severe ischemia alone helped identify 86% MTM-HCCs with a specificity of 66%. The average AUCs were 0.81 (95% CI: 0.71, 0.90) for the regression-based diagnostic model, with a sensitivity of 57% and specificity of 92%. Conclusions Necrosis or severe ischemia was a sensitive imaging feature of MTM-HCC. Noninvasive prediction of this subtype can be achieved with good accuracy and excellent specificity when findings were combined.

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