Risk for Recurrence in Long-Term Follow-Up of Children after Liver Transplantation for Hepatoblastoma or Hepatocellular Carcinoma

Author:

Stefanowicz Marek1,Kaliciński Piotr1ORCID,Ismail Hor1,Kowalski Adam1,Broniszczak Dorota1,Szymczak Marek1,Pankowska-Woźniak Katarzyna1,Roszkiewicz Anna1,Święszkowska Ewa2,Kamińska Diana3,Szymańska Sylwia4ORCID,Kowalewski Grzegorz1ORCID

Affiliation:

1. Department of Pediatric Surgery and Organ Transplantation, The Children’s Memorial Health Institute, 04-730 Warsaw, Poland

2. Department of Oncology, The Children’s Memorial Health Institute, 04-730 Warsaw, Poland

3. Department of Gastroenterology, Hepatology, Nutritional Disorders and Pediatrics, The Children’s Memorial Health Institute, 04-730 Warsaw, Poland

4. Department of Pathomorphology, The Children’s Memorial Health Institute, 04-730 Warsaw, Poland

Abstract

The aim of this study was to assess the long-term results of liver transplantation (LT) in pediatric patients with unresectable hepatoblastoma (HB) or hepatocellular carcinoma (HCC) with special reference to the risk of tumor recurrence. We retrospectively analyzed data from 46 HB and 26 HCC patients who underwent LT between 1990 and 2022. In HCC patients, we compared outcomes depending on donor type. We evaluated the impact of a number of risk factors on recurrence-free survival after LT. Estimated patient survival after 5, 10, and 15 years was 82%, 73%, and 73% in the HB group and 79%, 75%, and 75% in the HCC group, respectively (p = 0.76). In the HCC group, living donor LT (LDLT) and deceased donor LT (DDLT) provided similar patient survival (p = 0.09). Estimated recurrence-free survival in patients who had three or fewer risk factors was significantly better than in patients with more than three risk factors (p = 0.0001). Adequate patient selection is necessary when considering LT for primary liver tumors in children. The presence of more than three risk factors is associated with a very high risk of recurrence and indicates poor prognosis, whereas extrahepatic disease may be considered a contraindication for transplantation.

Publisher

MDPI AG

Subject

Pediatrics, Perinatology and Child Health

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