SIR 2025
Transplant Interventions
Scientific Session
Pedram Keshavarz, MD
Postdoc Research Fellow
David Geffen School of Medicine At UCLA, United States
Zahra Mohammadi Goldar, MD
Postdoc Research Fellow
UCLA, United States
Steven S. Raman, MD, FSIR
Professor of Radiology, Urology and Surgery
David Geffen School of Medicine At UCLA, United States
Om Patel, None
Researcher
UCLA, United States
Aarib Shahab, None
Researcher
UCLA, United States
Annabel Chen, BS
Volunteer Research Assistant
UCLA David Geffen School of Medicine, United States
Vatche G. Agopian, MD
Professor of Transplant Hepatology
UCLA, United States
Richard Finn, MD
Professor of Medicine, Division of Hematology/Oncology
UCLA, United States
Justin McWilliams, MD, FSIR
Professor of Interventional Radiology
David Geffen School of Medicine at UCLA, United States
Jason Chiang, MD, PhD (he/him/his)
Assistant Professor
Interventional Radiology, UCLA, United States
David S.K. Lu, MD
Professor of Radiology
UCLA, United States
This study investigates the risk of recurrent hepatocellular carcinoma (HCC) after orthotopic liver transplant (OLT) and correlates HCC differentiation from pre-OLT locoregional therapy (LRT) (PreLRTBxTD) and explant biopsies with post-OLT recurrence rates and survival, based on LI-RADS 5 and histopathology findings.
Materials and Methods: This IRB-approved and HIPAA-compliant study cohort included 449 LI-RADS 5 confirmed HCC patients (mean age, 69 ± 8.3 years; 336 men) who underwent OLT at a United States tertiary center between January 2005 and 2022. Post-OLT, patients were categorized into three subcohorts: intrahepatic recurrence (IH-R), extrahepatic recurrence (EH-R), and non-recurrence (NR). PreLRTBxTD was available for 32.7% of the cohort (147/449), subdivided into well (n = 51) and moderately to poorly tumor differentiated (TD) (n = 96).
Results: The mean overall and post-recurrence HCC (rHCC) follow-ups were 101.3 ± 28.3 months [IQR: 38, 83 months] and 35.6 ± 43.1 months [IQR: 10, 46 months], respectively. rHCC occurred in 50 patients (11.1%, 50/449) including IH-R (38%, 19/50) and EH-R (62%, 31/50). Over 75% rHCC occurred within 48 months post-OLT. Survival post-OLT for EH-R and IH-R was 81.7 ± 63.6 months and 153.6 ± 38.4 months, respectively (HR 2.64, 95%CI 1.41-4.96; p = 0.0023). Moderately to poorly differentiated PreLRTBxTD comprised 78% (39/50) of post-OLT rHCC and was associated with higher recurrence and lower survival (HR 2.93, 95% CI: 0.98-8.70; p = 0.052; HR 0.36, 95% CI: 0.11-1.17; p = 0.08). Explant histopathology showed that 80% of rHCC tumors were moderately to poorly TD, predominantly among EH-R rHCC subcohort (93.5% vs. 63.1% in IH-R), and significantly associated with worse survival rate (HR: 4.2, 95%CI 2.20-8.14; p < 0.0001).
Conclusion:
In patients with LI-RADS 5 HCC prior to OLT, poorly differentiated HCC from pre-LRT biopsy was associated with a trend toward higher rates of post-OLT recurrence and lower survival. These findings emphasize the need for improved noninvasive biomarkers to detect aggressive HCC.