Prognostic Factors for 10-Year Survival in Patients With Hepatocellular Cancer Receiving Liver Transplantation.

Milan criteria alpha-fetoprotein expanded criteria radiological response recurrence

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2022
Historique:
received: 16 02 2022
accepted: 29 03 2022
entrez: 16 5 2022
pubmed: 17 5 2022
medline: 17 5 2022
Statut: epublish

Résumé

Long-term survival after liver transplantation (LT) for hepatocellular cancer (HCC) continues to increase along with the modification of inclusion criteria. This study aimed at identifying risk factors for 5- and 10-year overall and HCC-specific death after LT. A total of 1,854 HCC transplant recipients from 10 European centers during the period 1987-2015 were analyzed. The population was divided in three eras, defined by landmark changes in HCC transplantability indications. Multivariable logistic regression analyses were used to evaluate the significance of independent risk factors for survival. Five- and 10-year overall survival (OS) rates were 68.1% and 54.4%, respectively. Two-hundred forty-two patients (13.1%) had HCC recurrence. Five- and 10-year recurrence rates were 16.2% and 20.3%. HCC-related deaths peaked at 2 years after LT (51.1% of all HCC-related deaths) and decreased to a high 30.8% in the interval of 6 to 10 years after LT. The risk factors for 10-year OS were macrovascular invasion (OR = 2.71; P = 0.001), poor grading (OR = 1.56; P = 0.001), HCV status (OR = 1.39; P = 0.001), diameter of the target lesion (OR = 1.09; P = 0.001), AFP slope (OR = 1.63; P = 0.006), and patient age (OR = 0.99; P = 0.01). The risk factor for 10-year HCC-related death were AFP slope (OR = 4.95; P < 0.0001), microvascular (OR = 2.13; P < 0.0001) and macrovascular invasion (OR = 2.32; P = 0.01), poor tumor grading (OR = 1.95; P = 0.001), total number of neo-adjuvant therapies (OR = 1.11; P = 0.001), diameter of the target lesion (OR = 1.11; P = 0.002), and patient age (OR = 0.97; P = 0.001). When analyzing survival rates in function of LT era, a progressive improvement of the results was observed, with patients transplanted during the period 2007-2015 showing 5- and 10-year death rates of 26.8% and 38.9% (vs. 1987-1996, P < 0.0001; vs. 1997-2006, P = 0.005). LT generates long-term overall and disease-free survival rates superior to all other oncologic treatments of HCC. The role of LT in the modern treatment of HCC becomes even more valued when the follow-up period reaches at least 10 years. The results of LT continue to improve even when prudently widening the inclusion criteria for transplantation. Despite the incidence of HCC recurrence is highest during the first 5 years post-transplant, one-third of them occur later, indicating the importance of a life-long follow-up of these patients.

Sections du résumé

Background UNASSIGNED
Long-term survival after liver transplantation (LT) for hepatocellular cancer (HCC) continues to increase along with the modification of inclusion criteria. This study aimed at identifying risk factors for 5- and 10-year overall and HCC-specific death after LT.
Methods UNASSIGNED
A total of 1,854 HCC transplant recipients from 10 European centers during the period 1987-2015 were analyzed. The population was divided in three eras, defined by landmark changes in HCC transplantability indications. Multivariable logistic regression analyses were used to evaluate the significance of independent risk factors for survival.
Results UNASSIGNED
Five- and 10-year overall survival (OS) rates were 68.1% and 54.4%, respectively. Two-hundred forty-two patients (13.1%) had HCC recurrence. Five- and 10-year recurrence rates were 16.2% and 20.3%. HCC-related deaths peaked at 2 years after LT (51.1% of all HCC-related deaths) and decreased to a high 30.8% in the interval of 6 to 10 years after LT. The risk factors for 10-year OS were macrovascular invasion (OR = 2.71; P = 0.001), poor grading (OR = 1.56; P = 0.001), HCV status (OR = 1.39; P = 0.001), diameter of the target lesion (OR = 1.09; P = 0.001), AFP slope (OR = 1.63; P = 0.006), and patient age (OR = 0.99; P = 0.01). The risk factor for 10-year HCC-related death were AFP slope (OR = 4.95; P < 0.0001), microvascular (OR = 2.13; P < 0.0001) and macrovascular invasion (OR = 2.32; P = 0.01), poor tumor grading (OR = 1.95; P = 0.001), total number of neo-adjuvant therapies (OR = 1.11; P = 0.001), diameter of the target lesion (OR = 1.11; P = 0.002), and patient age (OR = 0.97; P = 0.001). When analyzing survival rates in function of LT era, a progressive improvement of the results was observed, with patients transplanted during the period 2007-2015 showing 5- and 10-year death rates of 26.8% and 38.9% (vs. 1987-1996, P < 0.0001; vs. 1997-2006, P = 0.005).
Conclusions UNASSIGNED
LT generates long-term overall and disease-free survival rates superior to all other oncologic treatments of HCC. The role of LT in the modern treatment of HCC becomes even more valued when the follow-up period reaches at least 10 years. The results of LT continue to improve even when prudently widening the inclusion criteria for transplantation. Despite the incidence of HCC recurrence is highest during the first 5 years post-transplant, one-third of them occur later, indicating the importance of a life-long follow-up of these patients.

Identifiants

pubmed: 35574299
doi: 10.3389/fonc.2022.877107
pmc: PMC9093683
doi:

Types de publication

Journal Article

Langues

eng

Pagination

877107

Informations de copyright

Copyright © 2022 Lai, Viveiros, Iesari, Vitale, Mennini, Onali, Hoppe-Lotichius, Colasanti, Manzia, Mocchegiani, Spoletini, Agnes, Vivarelli, Tisone, Ettorre, Mittler, Tsochatzis, Rossi, Cillo, Schaefer and Lerut.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Quirino Lai (Q)

General Surgery and Organ Transplantation Unit, Sapienza, Rome, Italy.

Andre Viveiros (A)

Department of Medicine I, Innsbruck University, Innsbruck, Austria.

Samuele Iesari (S)

Institut de Recherche Expérimental et Clinique (IREC), Université Catholique de Louvain, Brussels, Belgium.

Alessandro Vitale (A)

Department of Surgical, Oncological and Gastroenterological Sciences, Padua University, Padua, Italy.

Gianluca Mennini (G)

General Surgery and Organ Transplantation Unit, Sapienza, Rome, Italy.

Simona Onali (S)

UCL Institute for Liver and Digestive Health and Royal Free Sheila Sherlock Liver Centre, Royal Free Hospital, London, United Kingdom.

Maria Hoppe-Lotichius (M)

Klinik für Allgemein-, Viszeral- und Transplantationschirurgie, Mainz University, Mainz, Germany.

Marco Colasanti (M)

Division of General Surgery and Liver Transplantation, San Camillo Hospital, Rome, Italy.

Tommaso M Manzia (TM)

Department of Transplant Surgery, PTV University, Rome, Italy.

Federico Mocchegiani (F)

Unit of Hepatobiliary Surgery and Transplantation, Marche Polytechnic University, Ancona, Italy.

Gabriele Spoletini (G)

Catholic University - Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.

Salvatore Agnes (S)

Catholic University - Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.

Marco Vivarelli (M)

Unit of Hepatobiliary Surgery and Transplantation, Marche Polytechnic University, Ancona, Italy.

Giuseppe Tisone (G)

Department of Transplant Surgery, PTV University, Rome, Italy.

Giuseppe M Ettorre (GM)

Division of General Surgery and Liver Transplantation, San Camillo Hospital, Rome, Italy.

Jens Mittler (J)

Klinik für Allgemein-, Viszeral- und Transplantationschirurgie, Mainz University, Mainz, Germany.

Emmanuel Tsochatzis (E)

UCL Institute for Liver and Digestive Health and Royal Free Sheila Sherlock Liver Centre, Royal Free Hospital, London, United Kingdom.

Massimo Rossi (M)

General Surgery and Organ Transplantation Unit, Sapienza, Rome, Italy.

Umberto Cillo (U)

Department of Surgical, Oncological and Gastroenterological Sciences, Padua University, Padua, Italy.

Benedikt Schaefer (B)

Department of Medicine I, Innsbruck University, Innsbruck, Austria.

Jan P Lerut (JP)

Institut de Recherche Expérimental et Clinique (IREC), Université Catholique de Louvain, Brussels, Belgium.

Classifications MeSH