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Second Primary Malignancies After Commercial CAR T Cell Therapy: Analysis of FDA Adverse Events Reporting System (FAERS).

Magdi ElsallabMoataz EllithiMatthew A LunningChristopher D'AngeloJihyun MaMiguel-Ángel PeralesMatthew J FrigaultMarcela V Maus
Published in: Blood (2024)
Second primary malignancies (SPMs) were reported in 536 out of 12,394 (4.3%) adverse event reports following CAR T cell therapies in the FDA Adverse Event Reporting System (FAERS). Myeloid and T-cell neoplasms were disproportionately more frequently reported, warranting further follow-up.
Keyphrases
  • cell therapy
  • adverse drug
  • stem cells
  • mesenchymal stem cells
  • electronic health record
  • bone marrow
  • emergency department
  • acute myeloid leukemia
  • immune response
  • drug administration