Background/Aims: Adjuvant systemic therapy has been proposed in patients at high-risk of hepatocellular carcinoma (HCC) recurrence. This study assessed the outcomes of a real-world cohort treated with either resection or ablation, stratified according to the IMbrave050 trial criteria. Methods: We selected, from the Italian Liver Cancer database, 1150 patients with HCC treated with upfront resection (n = 483, 64.2 % high-risk) or ablation (n = 667, 49.6 % high risk), fulfilling the inclusion criteria of the IMbrave050 trial. Results: Median recurrence-free survival (RFS) was shorter in high-risk resected patients (29.0 vs. 43.0 months; p = 0.024), while no difference was observed after ablation (27.0 vs. 30.0 months; p = 0.098). Recurrence was borderline higher in high-risk resected patients [Hazard Ratio (HR) 1.26, 0.97–1.23; p = 0.052], but not ablated ones (HR 1.13, 0.92–1.38; p = 0.221). Independent predictors of recurrence were cirrhosis (HR 1.52, 1.13–2.05), multinodular HCC (HR 1.31, 1.14–1.52), and microvascular invasion (HR 1.39, 1.05–1.83) in resected, and alpha-fetoprotein (HR 1.15, 1.07–1.23) in ablated patients. Median overall survival was similar in resected risk-groups (147.0 vs. 130.0 months; p = 0.093), shorter in high-risk ablated patients (79.0 vs. 98.0 months; p = 0.021). Conclusions: The criteria used to assess HCC recurrence risk in the IMbrave050 trial find validation by real-world data in patients treated with resection, while they are inaccurate after ablation.

Recurrence rate, features, and outcome after hepatocellular carcinoma curative resection or ablation according to the IMbrave050 criteria: a real-world study / Giannini, E.G., Pasta, A., Bucci, L., Plaz Torres, M.C., Pieri, G., Celsa, C., Sangiovanni, A., Piscaglia, F., Campani, C., Missale, G., Vidili, G., Ghittoni, G., Pelizzaro, F., Foschi, F.G., Morisco, F., Santi, V., Svegliati-Baroni, G., Azzaroli, F., Saitta, C., Brunetto, M.R., et al.. - In: DIGESTIVE AND LIVER DISEASE. - ISSN 1590-8658. - 57:8(2025), pp. 1673-1682. [10.1016/j.dld.2025.05.032]

Recurrence rate, features, and outcome after hepatocellular carcinoma curative resection or ablation according to the IMbrave050 criteria: a real-world study

Svegliati-Baroni, Gianluca;Allegrini, Gloria
Membro del Collaboration Group
;
Scorzoni, Chiara
Membro del Collaboration Group
;
Scandali, Giulia
Membro del Collaboration Group
;
Guarino, Maria
Membro del Collaboration Group
;
Capasso, Mario
Membro del Collaboration Group
;
2025-01-01

Abstract

Background/Aims: Adjuvant systemic therapy has been proposed in patients at high-risk of hepatocellular carcinoma (HCC) recurrence. This study assessed the outcomes of a real-world cohort treated with either resection or ablation, stratified according to the IMbrave050 trial criteria. Methods: We selected, from the Italian Liver Cancer database, 1150 patients with HCC treated with upfront resection (n = 483, 64.2 % high-risk) or ablation (n = 667, 49.6 % high risk), fulfilling the inclusion criteria of the IMbrave050 trial. Results: Median recurrence-free survival (RFS) was shorter in high-risk resected patients (29.0 vs. 43.0 months; p = 0.024), while no difference was observed after ablation (27.0 vs. 30.0 months; p = 0.098). Recurrence was borderline higher in high-risk resected patients [Hazard Ratio (HR) 1.26, 0.97–1.23; p = 0.052], but not ablated ones (HR 1.13, 0.92–1.38; p = 0.221). Independent predictors of recurrence were cirrhosis (HR 1.52, 1.13–2.05), multinodular HCC (HR 1.31, 1.14–1.52), and microvascular invasion (HR 1.39, 1.05–1.83) in resected, and alpha-fetoprotein (HR 1.15, 1.07–1.23) in ablated patients. Median overall survival was similar in resected risk-groups (147.0 vs. 130.0 months; p = 0.093), shorter in high-risk ablated patients (79.0 vs. 98.0 months; p = 0.021). Conclusions: The criteria used to assess HCC recurrence risk in the IMbrave050 trial find validation by real-world data in patients treated with resection, while they are inaccurate after ablation.
2025
Adjuvant treatment; Overall survival; Recurrence-free survival; Response; Systemic therapy
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11566/349867
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