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Review
. 2025 Apr;26(4):e203-e213.
doi: 10.1016/S1470-2045(24)00715-0.

Non-ICANS neurological complications after CAR T-cell therapies: recommendations from the EBMT Practice Harmonisation and Guidelines Committee

Affiliations
Review

Non-ICANS neurological complications after CAR T-cell therapies: recommendations from the EBMT Practice Harmonisation and Guidelines Committee

Charlotte E Graham et al. Lancet Oncol. 2025 Apr.

Abstract

Neurological complications are an important concern in patients undergoing chimeric antigen receptor (CAR) T-cell therapy. Consensus guidelines inform the management of immune effector cell-associated neurotoxicity syndrome (ICANS). However, these guidelines are based on the early clinical experience with CD19 targeting CAR T cells in B-cell malignancies. In contrast, there are so far no published best practice recommendations on the current management of other non-classical neurological complications, which frequently develop after CAR T-cell infusion and cause clinically significant neurotoxicity. These non-classical neurological complications could be more prevalent because of additional CAR T-cell targets (eg, B cell maturation antigen [BCMA]), widened access, new indications in clinical development (including solid tumours in the CNS), and long-term follow-up. In this Review, the European Society for Blood and Marrow Transplantation (EBMT) Practice Harmonisation and Guidelines Committee provides recommendations on the management of CAR T-cell associated neurological complications that occur after treatment with the licensed CD19 and BCMA CAR T cells, as well as neurological toxicities that are emerging with CAR T cells in clinical trials for solid and haematological cancers. We address movement and neurocognitive toxicity, cranial nerve palsies, tumour inflammation-associated neurotoxicity, stroke, myelopathy, peripheral neuropathy, Guillain-Barré syndrome, fludarabine-associated neurotoxicity, and provide guidance on the psychological support for patients. CNS infections were excluded. The guidelines were developed based on the currently available literature and expert opinion. Recommendations are provided when possible, and areas for further research are highlighted to provide a framework to improve patient care.

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Conflict of interest statement

Declaration of interests RV reports consultancy for Takeda, Novartis, Gilead, and Seagen; participation in speakers bureau for Takeda, Janssen, Amgen, and Gilead; and travel grants from Takeda and Gilead. AAT has received honoraria for educational sessions from Gilead and MSD and support for attending meetings from Eli Lilly, Gilead, and Novartis. OP has received honoraria or travel support from Alexion, Gilead, Jazz, MSD, Neovii, Novartis, Pfizer, and Therakos; and has received research support from Incyte and Priothera; is member of advisory boards to Apogepha, Alexion, Equillium Bio, Jazz, Gilead, Novartis, MSD, Omeros, Orca Bio, Priothera, Sanofi, Shionogi, and Sobi. J-IH has served as a consultant for Sobi. GD has received honoraria from Gilead and Bristol Myers Squibb. IY-A has received honoraria from Novartis, Kite or Gilead, Janssen, and Bristol Myers Squibb. GO has received consulting fees from Novartis and Pfizer; travel support from Incyte; institutional research grant from Incyte; and honoraria from Bristol Myers Squibb, Incyte, Jazz, Novartis, Pfizer, and Sanofi. NWCJvdD has received research support from Janssen, AMGEN, Celgene, Novartis, Cellectis, and Bristol Myers Squibb and serves in advisory boards for Janssen, AMGEN, Celgene, Bristol Myers Squibb, Sanofi, Takeda, Roche, Novartis, Bayer, Adaptive, Merck, Kite Pharma, Pfizer, AbbVie, and Servier, all paid to their institution. CR reports consultancy for Kite or Gilead, Novartis, Bristol Myers Squibb, Autolus, Cellistic, and Johnson & Johnson. MJF reports consultancy with Kite or Gilead, Johnson & Johnson, Novartis, and Bristol Myers Squibb. ZP reports consultancy with Novartis and honoraria with Sanofi and Therakos.

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