Potential Role of Liver Transplantation for Child-Pugh Class A Hepatocellular Carcinoma: Prognosis and Medical

Akihiro Seki1, Tomoyoshi Chiba1, Shintaro Yagi2

  • 1Department of Gastroenterology, Kanazawa University Hospital, Kanazawa, Japan.

Insights

Many patients with Child-Pugh class A (CP-A) hepatocellular carcinoma (HCC) lose eligibility for liver transplantation (LT) before their liver decompensates. This highlights the need to re-evaluate LT criteria for HCC patients.

Area of Science:

  • Hepatology
  • Transplantation Surgery
  • Oncology

Background:

  • Liver transplantation (LT) in Japan for hepatocellular carcinoma (HCC) is currently limited to patients with decompensated cirrhosis.
  • Child-Pugh class A (CP-A) patients with HCC initially meet Japan's LT criteria but may progress.
  • Understanding the clinical course and LT eligibility changes in CP-A HCC is crucial.

Purpose of the Study:

  • To investigate the clinical course, prognosis, and medical expenditure of CP-A HCC patients initially meeting LT criteria.
  • To assess changes in oncological eligibility for LT during follow-up in this patient group.
  • To compare survival and costs between LT recipients and CP-A HCC subgroups.

Main Methods:

  • Retrospective analysis of HCC patients (2011-2021) at Kanazawa University Hospital.
  • Inclusion of 134 CP-A HCC patients, 45 CP-B HCC patients, and 6 LT recipients (age < 70 years).
  • Comparison of survival rates and cumulative HCC-related medical expenditures; definition of a transplantable period.

Main Results:

  • LT offered the best prognosis (5-year overall survival: 83.3%).
  • CP-A HCC patients progressing beyond criteria showed significantly reduced survival, similar to CP-B disease.
  • Of 53 progressing patients, only 22.6% maintained LT eligibility (median 10.6 months); early recurrence and high FIB-4 index predicted poor prognosis.

Conclusions:

  • A significant proportion of CP-A HCC patients lose LT eligibility before hepatic decompensation.
  • Further research is needed to explore potential LT benefits for selected compensated cirrhosis patients.
  • This study informs future discussions on expanding LT indications for HCC.
Abstract