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@ARTICLE{Rejeski:302989,
author = {K. Rejeski$^*$ and J. A. Hill and S. Dahiya and M. D. Jain},
title = {{N}oncanonical and mortality-defining toxicities of {CAR}
{T} cell therapy.},
journal = {Nature medicine},
volume = {31},
number = {7},
issn = {1078-8956},
address = {[New York, NY]},
publisher = {Springer Nature},
reportid = {DKFZ-2025-01436},
pages = {2132-2146},
year = {2025},
note = {2025 Jul;31(7):2132-2146},
abstract = {Chimeric antigen receptor (CAR) T cell therapy is
associated with a unique spectrum of toxicities that drive
morbidity, mortality and patient quality of life. Previous
efforts yielded consensus grading systems for the
prototypical immunotoxicities-namely, cytokine-release
syndrome (CRS) and immune effector cell-associated
neurotoxicity syndrome (ICANS). These grading systems set
the stage for severity-based and standardized treatment
protocols that have contributed to a reduction in the acute
toxicity burden of CAR T cell therapy and have enabled
outpatient administration. However, understanding of CAR T
cell therapy has since grown to encompass new targets, new
diseases and broader patient populations-including long-term
survivors. As side effects are better defined and novel
toxicities emerge, there is a need to understand their
mechanisms and standardize reporting to improve clinical
management. Here we review the current state of knowledge
for mortality-defining and rare toxicities of CAR T cell
therapies, beyond CRS and ICANS. We discuss mechanisms,
including on-target injury, cytokine-associated inflammation
and dysregulated recovery, and how these mechanisms affect
the timing and management of toxicities. Finally, we define
key unmet needs and delineate future priorities and research
directions.},
subtyp = {Review Article},
cin = {MU01},
ddc = {610},
cid = {I:(DE-He78)MU01-20160331},
pnm = {899 - ohne Topic (POF4-899)},
pid = {G:(DE-HGF)POF4-899},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40670774},
doi = {10.1038/s41591-025-03813-5},
url = {https://inrepo02.dkfz.de/record/302989},
}