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Expanding Selection Criteria in Deceased Donor Liver Transplantation for Hepatocellular Carcinoma: Long-term Follow-up of a National Registry and 2 Transplant Centers.
Wehrle, Chase J; Kusakabe, Jiro; Akabane, Miho; Maspero, Marianna; Zervos, Bobby; Modaresi Esfeh, Jamak; Whitsett Linganna, Maureen; Imaoka, Yuki; Khalil, Mazhar; Pita, Alejandro; Kim, Jaekeun; Diago-Uso, Teresa; Fujiki, Masato; Eghtesad, Bijan; Quintini, Cristiano; Kwon, Choon David; Pinna, Antonio; Aucejo, Federico; Miller, Charles; Mazzaferro, Vincenzo; Schlegel, Andrea; Sasaki, Kazunari; Hashimoto, Koji.
Affiliation
  • Wehrle CJ; Department of Surgery, Transplantation Center, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH.
  • Kusakabe J; Department of Surgery, Transplantation Center, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH.
  • Akabane M; Department of Surgery, Stanford University Hospital, Palo Alto, CA.
  • Maspero M; General Surgery and Liver Transplantation Unit, IRCCS Istituto Tumori, Milan, Italy.
  • Zervos B; Department of Liver Transplantation, Cleveland Clinic Weston Hospital, Weston, FL.
  • Modaresi Esfeh J; Department of Gastroenterology and Hepatology, Cleveland Clinic, Cleveland, OH.
  • Whitsett Linganna M; Department of Gastroenterology and Hepatology, Cleveland Clinic, Cleveland, OH.
  • Imaoka Y; Department of Surgery, Stanford University Hospital, Palo Alto, CA.
  • Khalil M; Department of Surgery, Transplantation Center, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH.
  • Pita A; Department of Surgery, Transplantation Center, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH.
  • Kim J; Department of Surgery, Transplantation Center, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH.
  • Diago-Uso T; Department of Surgery, Digestive Disease Institute, Transplantation Center, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates.
  • Fujiki M; Department of Surgery, Transplantation Center, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH.
  • Eghtesad B; Department of Surgery, Transplantation Center, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH.
  • Quintini C; Department of Surgery, Digestive Disease Institute, Transplantation Center, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates.
  • Kwon CD; Department of Surgery, Transplantation Center, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH.
  • Pinna A; Department of Liver Transplantation, Cleveland Clinic Weston Hospital, Weston, FL.
  • Aucejo F; Department of Surgery, Transplantation Center, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH.
  • Miller C; Department of Surgery, Transplantation Center, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH.
  • Mazzaferro V; General Surgery and Liver Transplantation Unit, IRCCS Istituto Tumori, Milan, Italy.
  • Schlegel A; Department of Surgery, Transplantation Center, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH.
  • Sasaki K; Department of Immunology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH.
  • Hashimoto K; Department of Surgery, Stanford University Hospital, Palo Alto, CA.
Transplantation ; 2024 Jun 04.
Article in En | MEDLINE | ID: mdl-38831488
ABSTRACT

BACKGROUND:

This study compares selection criteria for liver transplant (LT) for hepatocellular carcinoma (HCC) for inclusivity and predictive ability to identify the most permissive criteria that maintain patient outcomes.

METHODS:

The Scientific Registry of Transplant Recipients (SRTR) database was queried for deceased donor LT's for HCC (2003-2020) with 3-y follow-up; these data were compared with a 2-center experience. Milan, University of California, San Francisco (UCSF), 5-5-500, Up-to-seven (U7), HALT-HCC, and Metroticket 2.0 scores were calculated.

RESULTS:

Nationally, 26 409 patients were included, and 547 at the 2 institutions. Median SRTR-follow-up was 6.8 y (interquartile range 3.9-10.1). Three criteria allowed the expansion of candidacy versus Milan UCSF (7.7%, n = 1898), Metroticket 2.0 (4.2%, n = 1037), and U7 (3.5%, n = 828). The absolute difference in 3-y overall survival (OS) between scores was 1.5%. HALT-HCC (area under the curve [AUC] = 0.559, 0.551-0.567) best predicted 3-y OS although AUC was notably similar between criteria (0.506 < AUC < 0.527, Mila n = 0.513, UCSF = 0.506, 5-5-500 = 0.522, U7 = 0.511, HALT-HCC = 0.559, and Metroticket 2.0 = 0.520), as was Harrall's c-statistic (0.507 < c-statistic < 0.532). All scores predicted survival to P < 0.001 on competing risk analysis. Median follow-up in our enterprise was 9.8 y (interquartile range 7.1-13.3). U7 (13.0%, n = 58), UCSF (11.1%, n = 50), HALT-HCC (6.4%, n = 29), and Metroticket 2.0 (6.3%, n = 28) allowed candidate expansion. HALT-HCC (AUC = 0.768, 0.713-0.823) and Metroticket 2.0 (AUC = 0.739, 0.677-0.801) were the most predictive of recurrence. All scores predicted recurrence and survival to P < 0.001 using competing risk analysis.

CONCLUSIONS:

Less restrictive criteria such as Metroticket 2.0, UCSF, or U7 allow broader application of transplants for HCC without sacrificing outcomes. Thus, the criteria for Model for End-stage Liver Disease-exception points for HCC should be expanded to allow more patients to receive life-saving transplantation.

Full text: 1 Database: MEDLINE Language: En Journal: Transplantation Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Language: En Journal: Transplantation Year: 2024 Type: Article