Olaparib combined with immunotherapy for treating a patient with liver cancer carrying BRCA2 germline mutation: A case report

Medicine (Baltimore). 2020 Sep 18;99(38):e22312. doi: 10.1097/MD.0000000000022312.

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.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antineoplastic Agents, Immunological / therapeutic use*
  • Antineoplastic Combined Chemotherapy Protocols
  • Fatal Outcome
  • Genes, BRCA2
  • Germ-Line Mutation
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Liver Neoplasms / diagnostic imaging
  • Liver Neoplasms / drug therapy*
  • Liver Neoplasms / genetics
  • Male
  • Nivolumab / therapeutic use*
  • Phthalazines / therapeutic use*
  • Piperazines / therapeutic use*

Substances

  • Antineoplastic Agents, Immunological
  • Phthalazines
  • Piperazines
  • Nivolumab
  • olaparib