Should hypervascular incidentalomas detected on per-interventional cone beam computed tomography during intra-arterial therapies for hepatocellular carcinoma impact the treatment plan in patients waiting for liver transplantation?

Author:

Derbel Haytham1,Galletto Athena1,Mulé Sébastien1,Calderaro Julien1,Zaarour Youssef1,Saccenti Laetitia1,Ghosn Mario1,Reizine Edouard1,Blain Maxime1,Laurent Alexis1,Brustia Raffaele1,Leroy Vincent1,Amaddeo Giuliana1,Luciani Alain1,Tacher Vania1,Kobeiter Hicham1

Affiliation:

1. Henri Mondor University Hospital

Abstract

Abstract Background and objective Current guidelines do not indicate any comprehensive management of hepatic hypervascular incidentalomas (HVIs) discovered in hepatocellular carcinoma (HCC) patients during intra-arterial therapies (IAT). The objective of this study is to evaluate the prognostic value of HVIs detected on per-interventional cone beam computed tomography (CBCT) during IAT for HCC in patients waiting for liver transplantation (LT). Material and methods In this retrospective single-institutional study, all liver-transplanted HCC patients between January 2014 and December 2018 who received transarterial chemoembolization (TACE) or radioembolization (TARE) before LT were included. The number of ≥ 10 mm HCCs diagnosed on contrast-enhanced preinterventional imaging (PII) was compared to that detected on per-interventional CBCT with a nonparametric Wilcoxon test. The correlation between the presence of an HVI and histopathological criteria associated with poor prognosis (HPP) on liver explants was investigated using the chi-square test. Tumor recurrence (TR) and TR-related mortality were investigated using the chi-square test. Recurrence-free survival (RFS), TR-related survival (TRRS), and overall survival (OS) were assessed according to the presence of HVI using Kaplan‒Meier analysis. Results Among 63 included patients (average age: 59 ± 7 years, H/F = 50/13), 36 presented HVIs on per-interventional CBCT. The overall nodule detection rate of per-interventional CBCT was superior to that of PII (median at 3 [Q1:2, Q3:5] vs. 2 [Q1:1, Q3:3], respectively, p < 0.001). No significant correlation was shown between the presence of HVI and HPP (p = 0.34), TR (p = 0.095) and TR-related mortality (0.22). Kaplan‒Meier analysis did not show a significant impact of the presence of HVI on RFS (p = 0.07), TRRS (0.48), or OS (p = 0.14). Conclusion Detection of HVIs during IAT should not affect the IAT treatment plan in patients awaiting LT.

Publisher

Research Square Platform LLC

Reference54 articles.

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