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Regression of Glioblastoma after Chimeric Antigen Receptor T-Cell Therapy

Open access
Brown, Christine E., Alizadeh, Darya, Starr, Renate, Weng, Lihong, Wagner, Jamie R., Naranjo, Araceli, Ostberg, Julie R., Blanchard, M. Suzette, Kilpatrick, Julie, Simpson, Jennifer, Kurien, Anita, Priceman, Saul J., Wang, Xiuli, Harshbarger, Todd L., D’Apuzzo, Massimo, Ressler, Julie A., Jensen, Michael C., Barish, Michael E., Chen, Mike, Portnow, Jana, Forman, Stephen J., Badie, Behnam·2016·New England Journal of Medicine

Abstract

A patient with recurrent multifocal glioblastoma received chimeric antigen receptor (CAR)-engineered T cells targeting the tumor-associated antigen interleukin-13 receptor alpha 2 (IL13Rα2). Multiple infusions of CAR T cells were administered over 220 days through two intracranial delivery routes - infusions into the resected tumor cavity followed by infusions into the ventricular system. Intracranial infusions of IL13Rα2-targeted CAR T cells were not associated with any toxic effects of grade 3 or higher. After CAR T-cell treatment, regression of all intracranial and spinal tumors was observed, along with corresponding increases in levels of cytokines and immune cells in the cerebrospinal fluid. This clinical response continued for 7.5 months after the initiation of CAR T-cell therapy. (Funded by Gateway for Cancer Research and others; ClinicalTrials.gov number, NCT02208362 .).

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Metadata

Authors
Brown, C. E., Alizadeh, D., Starr, R., Weng, L., Wagner, J. R., Naranjo, A., Ostberg, J. R., Blanchard, M. S., Kilpatrick, J., Simpson, J., Kurien, A., Priceman, S. J., Wang, X., Harshbarger, T. L., D’Apuzzo, M., Ressler, J. A., Jensen, M. C., Barish, M. E., Chen, M., Portnow, J., Forman, S. J., & Badie, B.
Venue
New England Journal of Medicine
Published
2016-12-29
Volume
375
Issue
26
Pages
2561-2569
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2567424265
Cited by
1,836
References
0
FWCI
67.99
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Regression of Glioblastoma after Chimeric Antigen Receptor T-Cell Therapy. https://app.cochat.ai/papers/10.1056/nejmoa1610497
The paper
Brown, C. E., Alizadeh, D., Starr, R., Weng, L., Wagner, J. R., Naranjo, A., Ostberg, J. R., Blanchard, M. S., Kilpatrick, J., Simpson, J., Kurien, A., Priceman, S. J., Wang, X., Harshbarger, T. L., D’Apuzzo, M., Ressler, J. A., Jensen, M. C., Barish, M. E., Chen, M., . . . Badie, B. (2016). Regression of Glioblastoma after Chimeric Antigen Receptor T-Cell Therapy. New England Journal of Medicine. https://doi.org/10.1056/nejmoa1610497

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.