AI Article Synopsis

  • This study evaluated the influence of ABO blood types on the recurrence of hepatocellular carcinoma (HCC) in patients who underwent living donor liver transplantation (LDLT).
  • Researchers analyzed 856 patients from 2006 to 2016 and found that the ABO blood group did not significantly affect disease-free survival (DFS) or overall survival (OS) after LDLT.
  • Key factors impacting survival were identified as tumor size and microvascular invasion, while the study concluded that ABO blood type is not a predictive factor for the outcomes in these patients.

Article Abstract

Purpose: This study assessed whether or not the ABO blood type affects the incidence of HCC recurrence after living donor liver transplantation (LDLT).

Methods: This retrospective observational study included 856 patients with hepatocellular carcinoma (HCC) who underwent LDLT between January 2006 and December 2016 at the Asan Medical Center.

Results: This study included 324 patients (37.9%) with blood type A, 215 (25.1%) with blood type B, 210 (24.5%) with blood type O, and 107 (12.5%) with blood type AB. ABO-incompatible LT was performed in 136 (15.9%) patients. The independent risk factors for the disease-free survival (DFS) were maximal tumor diameter, microvascular invasion, and Milan criteria. The only independent risk factor for the overall survival (OS) was microvascular invasion. The ABO blood group did not affect the DFS (P = 0.978) or OS (P = 0.261). The DFS according to the ABO blood group did not differ significantly between the ABO-compatible (p = 0.701) and ABO-incompatible LDLT recipients (p = 0.147). The DFS according to the ABO blood group did not differ significantly between patients within the Milan criteria (p = 0.934) and beyond the Milan criteria (p = 0.525). The DFS did not differ significantly between recipients with and without type A blood (p = 0.941).

Conclusions: This study demonstrated that the ABO blood group system had no prognostic impact on the oncological outcomes of patients undergoing LT for HCC.

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Source
http://dx.doi.org/10.1007/s00595-024-02879-xDOI Listing

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