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  • 1
    In: Liver International, Wiley
    Kurzfassung: We aimed to develop a Transformer‐based deep learning (DL) network for prognostic stratification in hepatocellular carcinoma (HCC) patients undergoing RFA. Methods A Swin Transformer DL network was trained to establish associations between magnetic resonance imaging (MRI) datasets and the ground truth of microvascular invasion (MVI) based on 696 surgical resection (SR) patients with solitary HCC ≤3 cm, and was validated in an external cohort ( n = 180). The multiphase MRI‐based DL risk outputs using an optimal threshold of .5 was employed as a MVI classifier for prognosis stratification in the RFA cohort ( n = 180). Results Over 90% of all enrolled patients exhibited hepatitis B virus infection. Liver cirrhosis was significantly more prevalent in the RFA cohort compared to the SR cohort (72.2% vs. 44.1%, p 〈 .001). The MVI risk outputs exhibited good performance (area under the curve values = .938 and .883) for predicting MVI in the training and validation cohort, respectively. The RFA patients at high risk of MVI classified by the MVI classifier demonstrated significantly lower recurrence‐free survival (RFS) and overall survival rates at 1, 3 and 5 years compared to those classified as low risk ( p 〈 .001). Multivariate cox regression modelling of a‐fetoprotein 〉 20 ng/mL [hazard ratio (HR) = 1.53; 95% confidence interval (95% CI): 1.02–2.33, p = .047], high risk of MVI (HR = 3.76; 95% CI: 2.40–5.88, p 〈 .001) and unfavourable tumour location (HR = 2.15; 95% CI: 1.40–3.29, p = .001) yielded a c‐index of .731 (bootstrapped 95% CI: .667–.778) for evaluating RFS after RFA. Among the three risk factors, MVI was the most powerful predictor for intrahepatic distance recurrence. Conclusions The proposed MVI classifier can serve as a valuable imaging biomarker for prognostic stratification in early‐stage HCC patients undergoing RFA.
    Materialart: Online-Ressource
    ISSN: 1478-3223 , 1478-3231
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2024
    ZDB Id: 2124684-1
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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