Use of Chimeric Antigen Receptor T Cells as a Potential Therapeutic for Glioblastoma

Use of Chimeric Antigen Receptor T Cells as a Potential Therapeutic for Glioblastoma SCIENCE TIMES 6. Gilard V, Djoubairou BO, Lepetit A, et al. progressed. In this study, the patient was reported. This response continued Small versus large catheters for ventriculostomy in the underwent surgical resection of 3 out of for 7.5 mo after initiation of CAR T-cell management of intraventricular hemorrhage. World 5 progressive tumors. A Rickham catheter therapy. However, the tumor eventually Neurosurg. 2017;97:117-122. was placed into the resection cavity of one recurred at 4 intracranial sites that were 7. Honeybul S, Ho KM, Gillett G. Outcome following decompressive hemicraniectomy for malignant of the tumors through which the patient different and non-adjacent to initial cerebral infarction: ethical considerations. Stroke. received 6 cycles of autologous CAR T- tumors. 2015;46(9):2695-2698. 6 3 cells (2–10 × 10 cells/infusion) that had The paper by Brown et al provides been modified to target the IL13Rα2. proof of concept for utilizing CAR T- The patient received 10 further doses cells in GBM. The route of delivery was Use of Chimeric Antigen through an intraventricular catheter after 2 shown to be important as intracavitary nonresected lesions continued to progress infusion appeared to act locally while Receptor T Cells as a and 2 new lesions appeared. Cerebrospinal intraventricular http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Neurosurgery Oxford University Press

Use of Chimeric Antigen Receptor T Cells as a Potential Therapeutic for Glioblastoma

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Publisher
Congress of Neurological Surgeons
Copyright
Copyright © 2017 by the Congress of Neurological Surgeons
ISSN
0148-396X
eISSN
1524-4040
D.O.I.
10.1093/neuros/nyx105
Publisher site
See Article on Publisher Site

Abstract

SCIENCE TIMES 6. Gilard V, Djoubairou BO, Lepetit A, et al. progressed. In this study, the patient was reported. This response continued Small versus large catheters for ventriculostomy in the underwent surgical resection of 3 out of for 7.5 mo after initiation of CAR T-cell management of intraventricular hemorrhage. World 5 progressive tumors. A Rickham catheter therapy. However, the tumor eventually Neurosurg. 2017;97:117-122. was placed into the resection cavity of one recurred at 4 intracranial sites that were 7. Honeybul S, Ho KM, Gillett G. Outcome following decompressive hemicraniectomy for malignant of the tumors through which the patient different and non-adjacent to initial cerebral infarction: ethical considerations. Stroke. received 6 cycles of autologous CAR T- tumors. 2015;46(9):2695-2698. 6 3 cells (2–10 × 10 cells/infusion) that had The paper by Brown et al provides been modified to target the IL13Rα2. proof of concept for utilizing CAR T- The patient received 10 further doses cells in GBM. The route of delivery was Use of Chimeric Antigen through an intraventricular catheter after 2 shown to be important as intracavitary nonresected lesions continued to progress infusion appeared to act locally while Receptor T Cells as a and 2 new lesions appeared. Cerebrospinal intraventricular

Journal

NeurosurgeryOxford University Press

Published: May 1, 2017

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