Preoperative Prediction of Microvascular Invasion in Patients With Hepatocellular Carcinoma Based on Radiomics Nomogram Using Contrast-Enhanced Ultrasound

This study aimed to develop a radiomics nomogram based on contrast-enhanced ultrasound (CEUS) for preoperatively assessing microvascular invasion (MVI) in hepatocellular carcinoma (HCC) patients. A retrospective dataset of 313 HCC patients who underwent CEUS between September 20, 2016 and March 20,...

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Veröffentlicht in:Frontiers in oncology 2021-09, Vol.11, p.709339-709339
Hauptverfasser: Zhang, Di, Wei, Qi, Wu, Ge-Ge, Zhang, Xian-Ya, Lu, Wen-Wu, Lv, Wen-Zhi, Liao, Jin-Tang, Cui, Xin-Wu, Ni, Xue-Jun, Dietrich, Christoph F
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Sprache:eng
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Zusammenfassung:This study aimed to develop a radiomics nomogram based on contrast-enhanced ultrasound (CEUS) for preoperatively assessing microvascular invasion (MVI) in hepatocellular carcinoma (HCC) patients. A retrospective dataset of 313 HCC patients who underwent CEUS between September 20, 2016 and March 20, 2020 was enrolled in our study. The study population was randomly grouped as a primary dataset of 192 patients and a validation dataset of 121 patients. Radiomics features were extracted from the B-mode (BM), artery phase (AP), portal venous phase (PVP), and delay phase (DP) images of preoperatively acquired CEUS of each patient. After feature selection, the BM, AP, PVP, and DP radiomics scores (Rad-score) were constructed from the primary dataset. The four radiomics scores and clinical factors were used for multivariate logistic regression analysis, and a radiomics nomogram was then developed. We also built a preoperative clinical prediction model for comparison. The performance of the radiomics nomogram was evaluated calibration, discrimination, and clinical usefulness. Multivariate analysis indicated that the PVP and DP Rad-score, tumor size, and AFP (alpha-fetoprotein) level were independent risk predictors associated with MVI. The radiomics nomogram incorporating these four predictors revealed a superior discrimination to the clinical model (based on tumor size and AFP level) in the primary dataset (AUC: 0.849  . 0.690; p 
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2021.709339