4.6 Article

Liver transplant for hepatocellular carcinoma in the United States: Evolving trends over the last three decades

期刊

AMERICAN JOURNAL OF TRANSPLANTATION
卷 20, 期 1, 页码 220-230

出版社

WILEY
DOI: 10.1111/ajt.15576

关键词

clinical research; practice; liver disease; infectious; liver disease; malignant; liver transplantation; hepatology

资金

  1. US Department of Defense [CA150272P3]
  2. Accelerator Award [C9380/A26813]
  3. National Cancer Institute [P30-CA196521]
  4. Samuel Waxman Cancer Research Foundation [SAF2016-76390]
  5. Generalitat de Catalunya [SGR-1358]
  6. European Commission [667273-2]
  7. European Commission (EC) [667273-2]
  8. National Cancer Institute
  9. Samuel Waxman Cancer Research Foundation

向作者/读者索取更多资源

Hepatitis C virus infection has been the most common etiology in HCC-related liver transplantation (LT). Since 2014, direct-acting antivirals (DAAs) have dramatically improved HCV cure. We aimed to study the changing pattern of etiologies and impact in outcome in HCC-related LT according to HCV treatment-era through retrospective analysis of the Scientific Registry of Transplant Recipients (SRTR) database (1987-2017). A total of 27 855 HCC-related liver transplants were performed (median age 59 years, 77% male). In the DAA era (2014-2017) there has been a 14.6% decrease in LT for HCV-related HCC; however, HCV remains the most common etiology in 50% of cases. In the same era, there has been a 50% increase in LT for NAFLD-related HCC. Overall survival was significantly worse for HCV-related HCC compared to NAFLD-related HCC during pre-DAA era (2002-2013; P = .031), but these differences disappeared in the DAA era. In addition, HCV patients had a significant improvement in survival when comparing the DAA era with IFN era (P < .001). Independent predictors of survival were significantly different in the pre-DAA era (HCV, AFP, diabetes) than in the DAA era (tumor size). HCV-related HCC continues to be the main indication for LT in the DAA era, but patients' survival has significantly improved and is comparable to that of NAFLD-related HCC.

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