Nivolumab-induced aplastic anemia: A case report and literature review

Rachel R Comito1, Lynette A Badu1, Nicholas Forcello2

  • 11 23893 Hartford Hospital , Hartford, CT, USA.

Insights

Programmed cell death-1 receptor inhibitor nivolumab showed efficacy in various cancers. However, a glioblastoma patient developed aplastic anemia after treatment, highlighting a rare but serious adverse event.

Area of Science:

  • Oncology
  • Immunotherapy
  • Hematology

Background:

  • Immune checkpoint inhibitors, such as programmed cell death-1 (PD-1) receptor inhibitors, represent a significant advancement in cancer therapy.
  • These therapies have shown efficacy in various malignancies, including non-small-cell lung cancer and metastatic melanoma, offering improved clinical responses and a better safety profile than traditional chemotherapy.
  • While generally well-tolerated, immune checkpoint inhibitors can cause immune-mediated adverse effects, ranging from common symptoms like fatigue and rash to rarer, severe conditions like colitis, pneumonitis, and encephalitis.

Observation:

  • This report details a case involving a female patient diagnosed with glioblastoma multiforme.
  • The patient received nivolumab, a PD-1 receptor inhibitor, as part of her treatment regimen.

Findings:

  • Following treatment with nivolumab, the patient developed aplastic anemia.
  • Aplastic anemia is a rare but severe adverse event associated with PD-1 inhibitor therapy.

Implications:

  • This case underscores the importance of monitoring for rare but serious hematological adverse events in patients receiving PD-1 inhibitors.
  • Further research is warranted to understand the mechanisms underlying PD-1 inhibitor-induced aplastic anemia and to develop strategies for its prevention and management.
  • Clinicians should maintain a high index of suspicion for aplastic anemia in patients presenting with symptoms suggestive of bone marrow failure during or after PD-1 inhibitor therapy.