Liver international : official journal of the International Association for the Study of the Liver · 2025
Early Hemostatic Treatment Could Improve 30-Day Survival After Spontaneous Rupture of Hepatocellular Carcinoma.
СтатьяМногоцентровое исследованиеНаблюдательное исследованиеНазвание и аннотация: Перевод в очереди
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Commin Apolline, Metivier Chloé, Allaire Manon, Lubrano Jean, Claudinot Amandine, Coilly Audrey, Allard Marc-Antoine, Roux Charles, Scatton Olivier, Nault Jean Charles, Sutter Olivier, Ganne-Carrié Nathalie, Ngo Thuy Vi, Goff Valérie Le, Ali Zeineb Ben, Tedlaouti Husni, Papin Josephine, Habireche Marion, Lebedel Louise, Pérignon Claire, Dao Thông, Morello Rémy, Ollivier-Hourmand Isabelle
Аннотация
INTRODUCTION: Spontaneous rupture of hepatocellular carcinoma (SRHCC) presents a critical clinical challenge, with early haemostasis often difficult to achieve and limited data available on subsequent treatment strategies. This study aims to evaluate whether the initial hemostatic approach influences early prognosis and facilitates further treatment of HCC.
METHODS: This retroprospective multicentric cohort included patients with SRHCC since 2008. Cox and Kaplan-Meier models analysed factors associated with overall survival (OS).
RESULTS: 112 patients with SRHCC were included. Hemostatic treatment was administered in 54.4% of cases (83.6% embolization, 9.8% surgery and 6.6% embolization plus surgery). The 30-day mortality rate was 28.6%. Factors associated with 30-day mortality included ALBI score > 2 (HR = 4.23; p = 0.001), shock (HR = 2.37; p = 0.029), acute kidney injury (HR = 4.40; p = 0.003), and BCLC stage C/D (HR = 14.29; p = 0.010). Early hemostatic intervention was associated with improved 30-day survival (HR = 0.42; p = 0.033). Palliative care was initiated in 27% of patients (10% after embolization and 17% upon admission). One-third of patients received subsequent HCC treatment after a median of 84 days [IQR: 39-176] (55.3% surgery and 18.4% systemic therapy). Among these, 63% (n = 24) had undergone early hemostatic treatment. The one-year OS rate was 39.3%, the median follow-up duration was 136 days (95% CI: 20.3-739.5), and the median OS was 6.6 ± 4.1 months (95% CI: 0-14.8). Delayed HCC treatment following rupture significantly improved OS (HR = 0.35; 95% CI: 0.20-0.61; p < 0.001), particularly when surgery was performed (p < 0.0001).
CONCLUSION: Our results suggest that early hemostatic treatment could be beneficial after spontaneous rupture of HCC in well compensated patients.
TRIAL REGISTRATION: NCT06505291.
METHODS: This retroprospective multicentric cohort included patients with SRHCC since 2008. Cox and Kaplan-Meier models analysed factors associated with overall survival (OS).
RESULTS: 112 patients with SRHCC were included. Hemostatic treatment was administered in 54.4% of cases (83.6% embolization, 9.8% surgery and 6.6% embolization plus surgery). The 30-day mortality rate was 28.6%. Factors associated with 30-day mortality included ALBI score > 2 (HR = 4.23; p = 0.001), shock (HR = 2.37; p = 0.029), acute kidney injury (HR = 4.40; p = 0.003), and BCLC stage C/D (HR = 14.29; p = 0.010). Early hemostatic intervention was associated with improved 30-day survival (HR = 0.42; p = 0.033). Palliative care was initiated in 27% of patients (10% after embolization and 17% upon admission). One-third of patients received subsequent HCC treatment after a median of 84 days [IQR: 39-176] (55.3% surgery and 18.4% systemic therapy). Among these, 63% (n = 24) had undergone early hemostatic treatment. The one-year OS rate was 39.3%, the median follow-up duration was 136 days (95% CI: 20.3-739.5), and the median OS was 6.6 ± 4.1 months (95% CI: 0-14.8). Delayed HCC treatment following rupture significantly improved OS (HR = 0.35; 95% CI: 0.20-0.61; p < 0.001), particularly when surgery was performed (p < 0.0001).
CONCLUSION: Our results suggest that early hemostatic treatment could be beneficial after spontaneous rupture of HCC in well compensated patients.
TRIAL REGISTRATION: NCT06505291.