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Autor(en) / Beteiligte
Titel
Bioactivity and Safety of IL13R alpha 2-Redirected Chimeric Antigen Receptor CD8+ T Cells in Patients with Recurrent Glioblastoma
Ist Teil von
  • Clinical cancer research, 2015-09, Vol.21 (18), p.4062-4072
Erscheinungsjahr
2015
Quelle
EZB Electronic Journals Library
Beschreibungen/Notizen
  • Purpose: A first-in-human pilot safety and feasibility trial evaluating chimeric antigen receptor (CAR)-engineered, autologous primary human CD8+ cytotoxic T lymphocytes (CTL) targeting IL13R alpha 2 for the treatment of recurrent glioblastoma (GBM).Experimental Design: Three patients with recurrent GBM were treated with IL13(E13Y)-zetakine CD8+ CTL targeting IL13R alpha 2. Patients received up to 12 local infusions at a maximum dose of 108 CAR-engineered T cells via a catheter/reservoir system.Results: We demonstrate the feasibility of manufacturing sufficient numbers of autologous CTL clones expressing an IL13(E13Y)-zetakine CAR for redirected HLA-independent IL13R alpha 2-specific effector function for a cohort of patients diagnosed with GBM. Intracranial delivery of the IL13-zetakine+ CTL clones into the resection cavity of 3 patients with recurrent disease was well-tolerated, with manageable temporary brain inflammation. Following infusion of IL13-zetakine+ CTLs, evidence for transient anti-glioma responses was observed in 2 of the patients. Analysis of tumor tissue from 1 patient before and after T-cell therapy suggested reduced overall IL13R alpha 2 expression within the tumor following treatment. MRI analysis of another patient indicated an increase in tumor necrotic volume at the site of IL13-zetakine+ T-cell administration.Conclusions: These findings provide promising first-in-human clinical experience for intracranial administration of IL13R alpha 2-specific CAR T cells for the treatment of GBM, establishing a foundation on which future refinements of adoptive CAR T-cell therapies can be applied. Clin Cancer Res; 21(18); 4062-72. copyright 2015 AACR.
Sprache
Englisch
Identifikatoren
ISSN: 1078-0432
DOI: 10.1158/1078-0432.CCR-15-0428
Titel-ID: cdi_proquest_miscellaneous_1808653765
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