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Number of Pretransplant Therapeutic Plasma Exchange Sessions Increase the Recurrence Risk of Hepatocellular Carcinoma in ABO-Incompatible Living Donor Liver Transplantation.

Transplant international : official journal of the European Society for Organ Transplantation 2025 Vol.38() p. 14304

Yoo YJ, Kim DG, Min EK, Yim SH, Choi MC, Koh HH, Kang M, Lee JG, Kim MS, Joo DJ

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Previous studies have reported comparable oncologic outcome between ABO-incompatible (ABOi) living donor liver transplantation (LDLT) and ABO-compatible (ABOc) LDLT in patients with hepatocellular car

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  • 표본수 (n) 323
  • p-value P = 0.005
  • p-value P = 0.014
  • 95% CI 1.02-3.86

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BibTeX ↓ RIS ↓
APA Yoo YJ, Kim DG, et al. (2025). Number of Pretransplant Therapeutic Plasma Exchange Sessions Increase the Recurrence Risk of Hepatocellular Carcinoma in ABO-Incompatible Living Donor Liver Transplantation.. Transplant international : official journal of the European Society for Organ Transplantation, 38, 14304. https://doi.org/10.3389/ti.2025.14304
MLA Yoo YJ, et al.. "Number of Pretransplant Therapeutic Plasma Exchange Sessions Increase the Recurrence Risk of Hepatocellular Carcinoma in ABO-Incompatible Living Donor Liver Transplantation.." Transplant international : official journal of the European Society for Organ Transplantation, vol. 38, 2025, pp. 14304.
PMID 40881323

Abstract

Previous studies have reported comparable oncologic outcome between ABO-incompatible (ABOi) living donor liver transplantation (LDLT) and ABO-compatible (ABOc) LDLT in patients with hepatocellular carcinoma (HCC). We aimed to analyze the relationship between number of therapeutic plasma exchanges (TPE) before LDLT and HCC outcomes in ABOi LDLT. In this single-center retrospective study, 428 adult LDLT recipients with HCC were categorized into three groups according to ABO incompatibility and the number of pretransplant TPE: ABOc (n = 323), ABOi/TPE ≤5 (n = 75), and ABOi/TPE ≥6 (n = 30). The RFS and HCC recurrence rates were compared. Three groups showed similar characteristics in most demographics, pretransplant tumor markers and pathologies. The median initial isoagglutinin (IA) titer was 1:64 (range negative-1:512) in ABOi/TPE ≤5 group and 1:512 (range 1:128-1:4,096) in ABOi/TPE ≥6 group. Five-year RFS was significantly lower (75.7% vs. 72.7% vs. 50.0%, P = 0.005) and HCC recurrence was significantly higher in the ABOi/TPE ≥6 group than in the other groups(16.4% vs. 17.0% vs. 39.4%, P = 0.014). In multivariable Cox regression analysis, ABOi/TPE ≥6 was an independent risk factor for RFS (aHR 1.99, 95% CI:1.02-3.86, P = 0.042) and HCC recurrence (aHR 2.42, 95% CI:1.05-5.57, P = 0.037). More than six pretransplant TPE sessions may increase the risk of HCC recurrence after ABOi LDLT. Reducing TPE sessions to fewer than six should be considered while maintaining immunological stability through IA titer control.

MeSH Terms

Humans; Carcinoma, Hepatocellular; Liver Transplantation; Liver Neoplasms; Male; Female; Middle Aged; Living Donors; Retrospective Studies; ABO Blood-Group System; Plasma Exchange; Blood Group Incompatibility; Adult; Neoplasm Recurrence, Local; Aged; Risk Factors; Treatment Outcome

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