AI Article Synopsis

  • Immunotherapy and targeted therapies are promising options for patients with difficult-to-treat liver cancer, particularly when traditional treatments fail.
  • A 37-year-old man with hepatitis B and advanced liver cancer received a combination of pembrolizumab and lenvatinib initially, which improved his condition before the disease progressed.
  • Subsequent treatment with olaparib and nivolumab stabilized his disease and relieved pain, highlighting the potential for tailored therapies based on genetic mutations like BRCA2 in liver cancer management.

Article Abstract

Rationale: Immunotherapy and targeted therapy have attracted widespread attention in current clinical research, which could be considered as a good therapeutic option for treatment of refractory liver cancer.

Patient Concerns: The patient was a 37-year-old man with hepatitis B virus (HBV) infection. He was presented with hepatalgia and discomfort.

Diagnosis: The computed tomography showed multiple intrahepatic masses, indicating primary liver cancer with multiple intrahepatic metastases.

Interventions: After failed transarterial chemoembolization therapy, he was initially treated with immunotherapy pembrolizumab plus angiogenesis inhibitor lenvatinib, and after 3 months of treatment, the condition improved. However, the disease subsequently progressed. The next-generation sequencing identified a BRCA2 germline mutation in this patient. A poly (ADP-ribose) polymerase inhibitor, olaparib, plus nivolumab therapy was started and achieved stable disease.

Outcomes: The patient achieved stable disease and improvement in hepatalgia for 3 months after the combination treatment of Olaparib and nivolumab.

Conclusion: We identified a BRCA2 germline mutation in a patient with liver cancer. Our findings could offer an alternative management for patients with liver cancer harboring germline BRCA2 mutation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505406PMC
http://dx.doi.org/10.1097/MD.0000000000022312DOI Listing

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