Treatment of inoperable hepatocellular carcinoma with immunotherapy.

BMJ Case Rep

Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Palo Alto, California, USA.

Published: July 2019

AI Article Synopsis

  • Mortality rates from hepatocellular carcinoma (HCC) are on the rise in the USA, making it a significant cause of cancer-related deaths globally.
  • Early treatment options like liver resection or transplantation have high success rates, but issues such as poor screening and suboptimal care access contribute to more patients presenting with late-stage HCC.
  • A case study of a 66-year-old man with inoperable HCC showed that after receiving nivolumab immunotherapy, his alpha-fetoprotein levels normalized, indicating a positive response without adverse effects.

Article Abstract

In the USA, mortality associated with hepatocellular carcinoma (HCC) continues to rise. Globally, HCC is the third most common cause of cancer-related death. In early stages of HCC, hepatic resection or liver transplantation are the preferred treatment options with a high probability of recurrence-free postoperative course. However, ineffective screening of chronic liver diseases in high-risk populations, poor linkage to care and suboptimal HCC surveillance has led to increasing rates of late-stage HCC at clinical presentation or diagnosis amenable only to palliative and experimental treatment options. Our case is a 66-year-old man with chronic hepatitis C virus infection complicated by cirrhosis and inoperable HCC which was non-responsive to selective intrahepatic trans-arterial chemoembolisation by interventional radiology. Therefore, he was treated with nivolumab immunotherapy and demonstrated normalisation of previously elevated alpha-fetoprotein levels suggestive of at least a partial response to immunotherapy. No adverse events related to nivolumab immunotherapy were encountered.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6663214PMC
http://dx.doi.org/10.1136/bcr-2019-229744DOI Listing

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