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Updated: Jan 27, 2026

Generation of Human Chimeric Antigen Receptor Regulatory T Cells
Published on: January 3, 2025
Neurological toxicities associated with chimeric antigen receptor T-cell therapy
Daniel B Rubin1,2, Husain H Danish1,2, Ali Basil Ali1
1Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Chimeric antigen receptor T-cell therapy can cause neurological toxicity, including encephalopathy and focal deficits. Early recognition of these symptoms is crucial for oncologists and neurologists managing patients receiving this cancer treatment.
Area of Science:
- Oncology
- Neurology
- Immunotherapy
Background:
- Chimeric antigen receptor T-cell therapy is a vital treatment for relapsed/refractory malignancies.
- Neurological toxicity is a significant adverse event associated with this therapy.
Purpose of the Study:
- To characterize the neurological toxicity profile of chimeric antigen receptor T-cell therapy.
- To identify common neurological symptoms and associated findings in patients undergoing this treatment.
Main Methods:
- A cohort of 100 patients treated with chimeric antigen receptor T-cell therapy was analyzed.
- Data were collected through chart review and prospective observation up to 2 months post-transfusion.
Main Results:
- The most frequent neurological symptoms included encephalopathy (57%), headache (42%), tremor (38%), and aphasia (35%).
- Focal neurological deficits correlated with EEG abnormalities, FDG-PET hypometabolism, and elevated transcranial Doppler velocities.
- Structural neuroimaging was typically normal.
Conclusions:
- Focal neurological deficits are common after chimeric antigen receptor T-cell therapy.
- Awareness of these neurological toxicities is essential for clinicians managing patients receiving this advanced cancer therapy.
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