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Intraventricular CARv3-TEAM-E T Cells in Recurrent Glioblastoma
by
Curry, William T.
, Carter, Bob S.
, Nikiforow, Sarah
, Mount, Christopher W.
, Gallagher, Kathleen
, Choi, Bryan D.
, Gerstner, Elizabeth R.
, Leick, Mark B.
, Balaj, Leonora
, Frigault, Matthew J.
, Maus, Marcela V.
in
Allergy
/ Antigens
/ Biopsy
/ Brain cancer
/ Brain Tumor
/ Catheters
/ CD8-Positive T-Lymphocytes - metabolism
/ Chemotherapy
/ Chimeric antigen receptors
/ Clinical outcomes
/ Epidermal growth factor receptors
/ ErbB Receptors - antagonists & inhibitors
/ ErbB Receptors - genetics
/ ErbB Receptors - metabolism
/ Genetics
/ Genetics General
/ Glioblastoma
/ Glioblastoma - pathology
/ Glioblastoma - therapy
/ Glioma
/ Hematology
/ Humans
/ Immunology
/ Immunotherapy
/ Immunotherapy, Adoptive - adverse effects
/ Lymphocytes
/ Lymphocytes T
/ Magnetic resonance imaging
/ Neoplasm Recurrence, Local - therapy
/ Neurology
/ Neuroscience
/ Neurosurgery
/ Oncology
/ Radiation
/ Receptors, Antigen, T-Cell - genetics
/ Receptors, Antigen, T-Cell - therapeutic use
/ Receptors, Chimeric Antigen - therapeutic use
/ T-Cells
/ Teams
/ Toxicity
/ Treatments in Oncology
/ Tumors
2024
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Intraventricular CARv3-TEAM-E T Cells in Recurrent Glioblastoma
by
Curry, William T.
, Carter, Bob S.
, Nikiforow, Sarah
, Mount, Christopher W.
, Gallagher, Kathleen
, Choi, Bryan D.
, Gerstner, Elizabeth R.
, Leick, Mark B.
, Balaj, Leonora
, Frigault, Matthew J.
, Maus, Marcela V.
in
Allergy
/ Antigens
/ Biopsy
/ Brain cancer
/ Brain Tumor
/ Catheters
/ CD8-Positive T-Lymphocytes - metabolism
/ Chemotherapy
/ Chimeric antigen receptors
/ Clinical outcomes
/ Epidermal growth factor receptors
/ ErbB Receptors - antagonists & inhibitors
/ ErbB Receptors - genetics
/ ErbB Receptors - metabolism
/ Genetics
/ Genetics General
/ Glioblastoma
/ Glioblastoma - pathology
/ Glioblastoma - therapy
/ Glioma
/ Hematology
/ Humans
/ Immunology
/ Immunotherapy
/ Immunotherapy, Adoptive - adverse effects
/ Lymphocytes
/ Lymphocytes T
/ Magnetic resonance imaging
/ Neoplasm Recurrence, Local - therapy
/ Neurology
/ Neuroscience
/ Neurosurgery
/ Oncology
/ Radiation
/ Receptors, Antigen, T-Cell - genetics
/ Receptors, Antigen, T-Cell - therapeutic use
/ Receptors, Chimeric Antigen - therapeutic use
/ T-Cells
/ Teams
/ Toxicity
/ Treatments in Oncology
/ Tumors
2024
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Intraventricular CARv3-TEAM-E T Cells in Recurrent Glioblastoma
by
Curry, William T.
, Carter, Bob S.
, Nikiforow, Sarah
, Mount, Christopher W.
, Gallagher, Kathleen
, Choi, Bryan D.
, Gerstner, Elizabeth R.
, Leick, Mark B.
, Balaj, Leonora
, Frigault, Matthew J.
, Maus, Marcela V.
in
Allergy
/ Antigens
/ Biopsy
/ Brain cancer
/ Brain Tumor
/ Catheters
/ CD8-Positive T-Lymphocytes - metabolism
/ Chemotherapy
/ Chimeric antigen receptors
/ Clinical outcomes
/ Epidermal growth factor receptors
/ ErbB Receptors - antagonists & inhibitors
/ ErbB Receptors - genetics
/ ErbB Receptors - metabolism
/ Genetics
/ Genetics General
/ Glioblastoma
/ Glioblastoma - pathology
/ Glioblastoma - therapy
/ Glioma
/ Hematology
/ Humans
/ Immunology
/ Immunotherapy
/ Immunotherapy, Adoptive - adverse effects
/ Lymphocytes
/ Lymphocytes T
/ Magnetic resonance imaging
/ Neoplasm Recurrence, Local - therapy
/ Neurology
/ Neuroscience
/ Neurosurgery
/ Oncology
/ Radiation
/ Receptors, Antigen, T-Cell - genetics
/ Receptors, Antigen, T-Cell - therapeutic use
/ Receptors, Chimeric Antigen - therapeutic use
/ T-Cells
/ Teams
/ Toxicity
/ Treatments in Oncology
/ Tumors
2024
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Intraventricular CARv3-TEAM-E T Cells in Recurrent Glioblastoma
Journal Article
Intraventricular CARv3-TEAM-E T Cells in Recurrent Glioblastoma
2024
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Overview
In this first-in-human, investigator-initiated, open-label study, three participants with recurrent glioblastoma were treated with CARv3-TEAM-E T cells, which are chimeric antigen receptor (CAR) T cells engineered to target the epidermal growth factor receptor (EGFR) variant III tumor-specific antigen, as well as the wild-type EGFR protein, through secretion of a T-cell–engaging antibody molecule (TEAM). Treatment with CARv3-TEAM-E T cells did not result in adverse events greater than grade 3 or dose-limiting toxic effects. Radiographic tumor regression was dramatic and rapid, occurring within days after receipt of a single intraventricular infusion, but the responses were transient in two of the three participants. (Funded by Gateway for Cancer Research and others; INCIPIENT ClinicalTrials.gov number,
NCT05660369
.)
A novel CAR T-cell therapy directed at EGFRvIII with a secretable EGFR T-cell engager produced rapid responses in three patients with recurrent glioblastoma, but the responses were transient in two of the three.
Publisher
Massachusetts Medical Society
Subject
/ Antigens
/ Biopsy
/ CD8-Positive T-Lymphocytes - metabolism
/ Epidermal growth factor receptors
/ ErbB Receptors - antagonists & inhibitors
/ Genetics
/ Glioma
/ Humans
/ Immunotherapy, Adoptive - adverse effects
/ Neoplasm Recurrence, Local - therapy
/ Oncology
/ Receptors, Antigen, T-Cell - genetics
/ Receptors, Antigen, T-Cell - therapeutic use
/ Receptors, Chimeric Antigen - therapeutic use
/ T-Cells
/ Teams
/ Toxicity
/ Tumors
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