Abstract

BackgroundThe purpose of this study was to develop and validate a radiomics nomogram for preoperative differentiating focal nodular hyperplasia (FNH) from hepatocellular carcinoma (HCC) in the non-cirrhotic liver.MethodsA total of 156 patients with FNH (n = 55) and HCC (n = 101) were divided into a training set (n = 119) and a validation set (n = 37). Radiomics features were extracted from triphasic contrast CT images. A radiomics signature was constructed with the least absolute shrinkage and selection operator algorithm, and a radiomics score (Rad-score) was calculated. Clinical data and CT findings were assessed to build a clinical factors model. Combined with the Rad-score and independent clinical factors, a radiomics nomogram was constructed by multivariate logistic regression analysis. Nomogram performance was assessed with respect to discrimination and clinical usefulness.ResultsFour thousand two hundred twenty-seven features were extracted and reduced to 10 features as the most important discriminators to build the radiomics signature. The radiomics signature showed good discrimination in the training set (AUC [area under the curve], 0.964; 95% confidence interval [CI], 0.934–0.995) and the validation set (AUC, 0.865; 95% CI, 0.725–1.000). Age, Hepatitis B virus infection, and enhancement pattern were the independent clinical factors. The radiomics nomogram, which incorporated the Rad-score and clinical factors, showed good discrimination in the training set (AUC, 0.979; 95% CI, 0.959–0.998) and the validation set (AUC, 0.917; 95% CI, 0.800–1.000), and showed better discrimination capability (P < 0.001) compared with the clinical factors model (AUC, 0.799; 95% CI, 0.719–0.879) in the training set. Decision curve analysis showed the nomogram outperformed the clinical factors model in terms of clinical usefulness.ConclusionsThe CT-based radiomics nomogram, a noninvasive preoperative prediction tool that incorporates the Rad-score and clinical factors, shows favorable predictive efficacy for differentiating FNH from HCC in the non-cirrhotic liver, which might facilitate clinical decision-making process.

Highlights

  • The purpose of this study was to develop and validate a radiomics nomogram for preoperative differentiating focal nodular hyperplasia (FNH) from hepatocellular carcinoma (HCC) in the non-cirrhotic liver

  • 80% of cases of HCC occur in patients with liver cirrhosis, arising from hepatitis B and C infections or alcoholism [2, 3]

  • In patients with liver cirrhosis, noninvasive diagnosis of HCC can be established by a characteristic feature of arterial phase hyperenhancement followed by portal venous or delayed phase washout on multiphasic contrast CT or MRI

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Summary

Introduction

The purpose of this study was to develop and validate a radiomics nomogram for preoperative differentiating focal nodular hyperplasia (FNH) from hepatocellular carcinoma (HCC) in the non-cirrhotic liver. 80% of cases of HCC occur in patients with liver cirrhosis, arising from hepatitis B and C infections or alcoholism [2, 3]. An increasing number of HCC arises in a non-cirrhotic liver [3], probably due to transient hepatitis B infection or due to diffuse liver damage caused by non-alcoholic fatty liver disease. In such non-cirrhotic cases, other benign hypervascular liver lesions (hepatocellular adenoma [HCA] and focal nodular hyperplasia [FNH]) should be taken into the differential diagnosis. The distinction between HCC and FNH is critical as the management differs considerably

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