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Validation of the alpha-Fetoprotein Model for Hepatocellular Carcinoma Recurrence after Transplantation in an Asian Population

J. Rhu, J. Kim, G. Choi, C. Kwon, J. Joh, S. Kim.

Department of Surgery, Samsung Medical Center, Seoul, Republic of Korea.

Meeting: 2018 American Transplant Congress

Abstract number: C220

Keywords: Hepatocellular carcinoma

Session Information

Session Name: Poster Session C: Liver: Recipient Selection

Session Type: Poster Session

Date: Monday, June 4, 2018

Session Time: 6:00pm-7:00pm

 Presentation Time: 6:00pm-7:00pm

Location: Hall 4EF

Background: This study was designed to validate the alpha-fetoprotein model for predicting recurrence after LT in Korean HCC patients.

Methods: Patients who underwent liver transplantation for HCC at Samsung Medical Center between 2007 and 2015 were included. Recurrence, overall survival, and disease-specific survival of patients divided by both the Milan criteria and the alpha-fetoprotein model were compared using Kaplan-Meier log-rank test. The predictability of the alpha-fetoprotein model compared to the Milan criteria was tested by means of net reclassification improvement analysis applied to patients with a follow-up of at least 2 years.

Results: A total of 400 patients were included in the study. Patients within Milan criteria had 5-year recurrence, overall survival, and disease-specific survival rates of 20.9%, 76.3%, and 89.4%, respectively, compared to corresponding rates of 50.3%, 55.7%, and 64.4%, respectively, for patients who were beyond Milan criteria. Alpha-fetoprotein model low risk patients had 5-year recurrence, overall survival, and disease-specific survival rates of 21.1%, 76.2%, and 89.3%, respectively, compared to corresponding rates of 57.7%, 52.2%, and 59.3%, respectively, in high risk patients (P<0.001, all). Although overall net reclassification improvements were statistically nonsignificant for recurrence (NRI=1.7%,Z=0.30,p=0.7624), overall survival (NRI=9.0%,Z=1.60,p=0.1098), and disease-specific survival (NRI=9.5%,Z=1.34,p=0.1807), they were significantly better for predicting no recurrence (NRI=6.6%,Z=3.16,p=0.0016), no death (NRI=7.7%,Z=3.65,p=0.0003), and no recurrence-related death (NRI=6.9%,Z=3.37,p=0.0007).

Conclusions: The alpha-fetoprotein model seems to be a promising tool for liver transplantation candidacy, but further investigation is needed.

CITATION INFORMATION: Rhu J., Kim J., Choi G., Kwon C., Joh J., Kim S. Validation of the alpha-Fetoprotein Model for Hepatocellular Carcinoma Recurrence after Transplantation in an Asian Population Am J Transplant. 2017;17 (suppl 3).

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To cite this abstract in AMA style:

Rhu J, Kim J, Choi G, Kwon C, Joh J, Kim S. Validation of the alpha-Fetoprotein Model for Hepatocellular Carcinoma Recurrence after Transplantation in an Asian Population [abstract]. https://atcmeetingabstracts.com/abstract/validation-of-the-alpha-fetoprotein-model-for-hepatocellular-carcinoma-recurrence-after-transplantation-in-an-asian-population/. Accessed May 15, 2025.

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