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Charting the Path Forward for Risk Prediction in Liver Transplant for Hepatocellular Carcinoma: International Validation of HALTHCC Among 4,089 Patients

  • D. J. Firl
  • , K. Sasaki*
  • , V. G. Agopian
  • , A. Gorgen
  • , S. Kimura
  • , W. Dumronggittigule
  • , J. C. McVey
  • , S. Iesari
  • , G. Mennini
  • , A. Vitale
  • , A. Finkenstedt
  • , S. Onali
  • , M. Hoppe-Lotichius
  • , G. Vennarecci
  • , T. M. Manzia
  • , D. Nicolini
  • , Alfonso Wolfango Avolio
  • , Salvatore Agnes
  • , M. Vivarelli
  • , G. Tisone
  • G. M. Ettorre, G. Otto, E. Tsochatzis, M. Rossi, A. Viveiros, U. Cillo, J. F. Markmann, T. Ikegami, T. Kaido, Q. Lai, G. Sapisochin, J. Lerut, F. N. Aucejo
*Corresponding author
  • Cleveland Clinic Lerner College of Medicine of Case Western University
  • University of Toronto
  • Department of Molecular Biology
  • University of California at Los Angeles
  • Université catholique de Louvain
  • Azienda Ospedaliero-Universitaria Policlinico Umberto I
  • University of Padua
  • Innsbruck Medical University
  • The Royal Free Hospital
  • Johannes Gutenberg University Mainz
  • San Camillo Hospital
  • Ospedali Riuniti
  • University of Rome Tor Vergata
  • Kyoto University
  • Kyushu University

Research output: Contribution to journalArticlepeer-review

Abstract

Prognosticating outcomes in liver transplant (LT) for hepatocellular carcinoma (HCC) continues to challenge the field. Although Milan Criteria (MC) generalized the practice of LT for HCC and improved outcomes, its predictive character has degraded with increasing candidate and oncological heterogeneity. We sought to validate and recalibrate a previously developed, preoperatively calculated, continuous risk score, the Hazard Associated with Liver Transplantation for Hepatocellular Carcinoma (HALTHCC), in an international cohort. From 2002 to 2014, 4,089 patients (both MC in and out [25.2%]) across 16 centers in North America, Europe, and Asia were included. A continuous risk score using pre-LT levels of alpha-fetoprotein, Model for End-Stage Liver Disease Sodium score, and tumor burden score was recalibrated among a randomly selected cohort (n = 1,021) and validated in the remainder (n = 3,068). This study demonstrated significant heterogeneity by site and year, reflecting practice trends over the last decade. On explant pathology, both vascular invasion (VI) and poorly differentiated component (PDC) increased with increasing HALTHCC score. The lowest-risk patients (HALTHCC 0-5) had lower rates of VI and PDC than the highest-risk patients (HALTHCC > 35) (VI, 7.7%[ 1.2-14.2] vs. 70.6% [48.3-92.9] and PDC:4.6% [0.1%-9.8%] vs. 47.1% [22.6-71.5]; P < 0.0001 for both). This trend was robust to MC status. This international study was used to adjust the coefficients in the HALTHCC score. Before recalibration, HALTHCC had the greatest discriminatory ability for overall survival (OS; C-index = 0.61) compared to all previously reported scores. Following recalibration, the prognostic utility increased for both recurrence (C-index = 0.71) and OS (C-index = 0.63). Conclusion: This large international trial validated and refined the role for the continuous risk metric, HALTHCC, in establishing pre-LT risk among candidates with HCC worldwide. Prospective trials introducing HALTHCC into clinical practice are warranted.
Original languageEnglish
Pages (from-to)569-582
Number of pages14
JournalHepatology
Volume71
Issue number2
DOIs
Publication statusPublished - 2020

All Science Journal Classification (ASJC) codes

  • Hepatology

Keywords

  • HEPATOCELLULAR CARCINOMA
  • LIVER TRANSPLANTATION
  • OUTCOME
  • PROGNOSTIC SCORE
  • RISK FACTORS

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