Olaparib induced aplastic anemia in a patient with castrate resistant prostate cancer: A case report

Elrazi A Ali1, Monika Jain1, Akriti Pokhrel2

  • 1Internal Medicine Department, Interfaith Medical Center, One Brooklyn Health, Brooklyn, NY, USA.

PubMed

Insights

Olaparib, a PARP inhibitor, treats prostate cancer but can cause rare side effects. This case report details a patient who developed aplastic anemia after olaparib treatment for BRCA2-positive cancer.

Area of Science:

  • Oncology
  • Pharmacology
  • Genetics

Background:

  • Olaparib is a poly (ADP-ribose) polymerase inhibitor (PARPi) approved for metastatic castration-resistant prostate cancer (CRPC).
  • PARPi therapy targets cancer cells with BRCA1/BRCA2 mutations or homologous recombination deficiency by inhibiting DNA repair.
  • While myelodysplastic syndrome and acute leukemia have been reported with PARPi use, aplastic anemia is not a commonly associated adverse event.

Observation:

  • A 75-year-old male patient with BRCA2-positive metastatic CRPC received olaparib treatment.
  • The patient subsequently developed aplastic anemia.

Findings:

  • This case report documents the first instance of aplastic anemia following olaparib therapy in a patient with prostate cancer.
  • The patient's BRCA2 mutation status and the mechanism of PARPi action are key considerations.

Implications:

  • This finding expands the known spectrum of potential adverse events associated with olaparib and PARP inhibitors.
  • Further investigation into the risk of aplastic anemia in patients receiving PARPi therapy is warranted.
  • Clinical monitoring for hematological toxicities should be vigilant in patients undergoing PARPi treatment.