Liver transplantation for HCC: validation of prognostic power of the RETREAT score for recurrence in a UK cohort.


Journal

HPB : the official journal of the International Hepato Pancreato Biliary Association
ISSN: 1477-2574
Titre abrégé: HPB (Oxford)
Pays: England
ID NLM: 100900921

Informations de publication

Date de publication:
05 2022
Historique:
received: 18 05 2021
revised: 23 08 2021
accepted: 08 09 2021
pubmed: 28 10 2021
medline: 12 5 2022
entrez: 27 10 2021
Statut: ppublish

Résumé

The Risk Estimation of Tumor Recurrence After Transplant (RETREAT) score as a prognostic index for recurrence has been reported previously and has not been validated outside the USA. Our study has validated the score in a single center UK cohort of patients being transplanted for HCC. LT for HCC between 2008 and 2018 at our center were analyzed. Recurrence-free survival (RFS) was compared by the RETREAT score and validated using Net Reclassification Improvement (NRI) by comparing it to Milan criteria. 346 adult HCC patients were transplanted of whom 313 were included. 28 (8.9%) had a recurrence. Summation of largest diameter and total number of viable tumors (HR = 1.19, p < 0.001), micro-/macro-vascular invasion (HR = 3.74, p = 0.002) and AFP>20 ng/ml (HR = 3.03, p = 0.005) were associated with recurrence on multivariate analysis. RFS decreased with increasing RETREAT score (log-rank p = 0.016). RETREAT performed better than Milan with significant NRI at 1- and 2-years post-transplant (0.43 (p = 0.004) and 0.38 (p = 0.03) respectively). LT outcomes using the revised UK criteria are equivalent to Milan criteria. Further, RETREAT score was validated as a prognostic index for the first time in a UK cohort and may assist risk stratification, selection for adjuvant therapies and guide surveillance.

Sections du résumé

BACKGROUND
The Risk Estimation of Tumor Recurrence After Transplant (RETREAT) score as a prognostic index for recurrence has been reported previously and has not been validated outside the USA. Our study has validated the score in a single center UK cohort of patients being transplanted for HCC.
METHODS
LT for HCC between 2008 and 2018 at our center were analyzed. Recurrence-free survival (RFS) was compared by the RETREAT score and validated using Net Reclassification Improvement (NRI) by comparing it to Milan criteria.
RESULTS
346 adult HCC patients were transplanted of whom 313 were included. 28 (8.9%) had a recurrence. Summation of largest diameter and total number of viable tumors (HR = 1.19, p < 0.001), micro-/macro-vascular invasion (HR = 3.74, p = 0.002) and AFP>20 ng/ml (HR = 3.03, p = 0.005) were associated with recurrence on multivariate analysis. RFS decreased with increasing RETREAT score (log-rank p = 0.016). RETREAT performed better than Milan with significant NRI at 1- and 2-years post-transplant (0.43 (p = 0.004) and 0.38 (p = 0.03) respectively).
CONCLUSION
LT outcomes using the revised UK criteria are equivalent to Milan criteria. Further, RETREAT score was validated as a prognostic index for the first time in a UK cohort and may assist risk stratification, selection for adjuvant therapies and guide surveillance.

Identifiants

pubmed: 34702624
pii: S1365-182X(21)01628-2
doi: 10.1016/j.hpb.2021.09.008
pii:
doi:

Substances chimiques

alpha-Fetoproteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

596-605

Informations de copyright

Crown Copyright © 2021. Published by Elsevier Ltd. All rights reserved.

Auteurs

Shruthi H S Reddy (SHS)

Liver Transplant Surgery, Institute of Liver Studies, King's College Hospital, London, SE5 9RS, United Kingdom.

Neil Mehta (N)

Hepatology, Department of Medicine, University of California, San Francisco, United States.

Jennifer L Dodge (JL)

Biostatistics, Department of Medicine and Preventive Medicine, University of Southern California, Los Angeles, United States.

Abdul R Hakeem (AR)

Hepatobiliary and Liver Transplant Surgery, St James's University Hospital, Leeds, LS97TF, United Kingdom.

Shirin E Khorsandi (SE)

Liver Transplant Surgery, Institute of Liver Studies, King's College Hospital, London, SE5 9RS, United Kingdom; Institute of Hepatology, Foundation for Liver Research, London, United Kingdom.

Wayel Jassem (W)

Liver Transplant Surgery, Institute of Liver Studies, King's College Hospital, London, SE5 9RS, United Kingdom.

Hector Vilca-Melendez (H)

Liver Transplant Surgery, Institute of Liver Studies, King's College Hospital, London, SE5 9RS, United Kingdom.

Miriam Cortes-Cerisuelo (M)

Liver Transplant Surgery, Institute of Liver Studies, King's College Hospital, London, SE5 9RS, United Kingdom.

Parthi Srinivasan (P)

Liver Transplant Surgery, Institute of Liver Studies, King's College Hospital, London, SE5 9RS, United Kingdom.

Andreas Prachalias (A)

Liver Transplant Surgery, Institute of Liver Studies, King's College Hospital, London, SE5 9RS, United Kingdom.

Michael A Heneghan (MA)

Hepatology, Institute of Liver Studies, King's College Hospital, London, United Kingdom.

Varuna Aluvihare (V)

Hepatology, Institute of Liver Studies, King's College Hospital, London, United Kingdom.

Abid Suddle (A)

Hepatology, Institute of Liver Studies, King's College Hospital, London, United Kingdom.

Rosa Miquel (R)

Liver Histopathology, Department of Histopathology, Institute of Liver Studies, King's College Hospital, London, United Kingdom.

Mohamed Rela (M)

Liver Transplant and HPB Surgery, Dr Rela Institute & Medical Center, Chennai, India.

Nigel D Heaton (ND)

Liver Transplant Surgery, Institute of Liver Studies, King's College Hospital, London, SE5 9RS, United Kingdom.

Krishna V Menon (KV)

Liver Transplant Surgery, Institute of Liver Studies, King's College Hospital, London, SE5 9RS, United Kingdom. Electronic address: krishna.menon@nhs.net.

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