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Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography
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Second primary malignancies after commercial CAR T-cell therapy: analysis of the FDA Adverse Events Reporting System
Magdi Elsallab1,2, Moataz Ellithi3, Matthew A Lunning3
1Harvard-MIT Center for Regulatory Science, Harvard Medical School, Boston, MA.
Blood
|March 14, 2024
Abstract:
Second primary malignancies were reported in 536 of 12 394 (4.3%) adverse event reports following chimeric antigen receptor T-cell therapies in the Food and Drug Administration Adverse Event Reporting System. Myeloid and T-cell neoplasms were disproportionately more frequently reported, warranting further follow-up.

