4.5 Review

DCVax®-L-Developed by Northwest Biotherapeutics

Journal

HUMAN VACCINES & IMMUNOTHERAPEUTICS
Volume 10, Issue 11, Pages 3139-3145

Publisher

TAYLOR & FRANCIS INC
DOI: 10.4161/hv.29276

Keywords

DCVax (R)-L; glioblastoma multiforme; immunotherapy; vaccine; dendritic cells; overall survival; side effects; BBB; blood brain barrier; CNS; central nervous system; CTL; cytotoxic T-lymphocyte; DC; dendritic cell; DTH; delayed tissue hypersensitivity; EORTC; European Organization for Research and Treatment of Cancer; FDA; Food and Drug Administration; GBM; glioblastoma multiforme; GM-CSF; granulocyte-macrophage colony-stimulating factor; HGG; high-grade glioma; IL-4; interleukin-4; IMP; investigational medicinal product; MHRA; Medicines and Healthcare products Regulatory Agency; MRI; magnetic resonance imaging; ND; newly diagnosed; NIHR; National Institute for Health Research; NWBT; Northwest Biotherapeutics Inc; OS; overall survival; PEI; Paul-Ehrlich-Institute; PFS; progression-free survival; TAAs; tumor-associated antigens; UCLA; University of California; Los Angeles; U; S; A; United States of America

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Dendritic cell (DC) immunotherapy is emerging as a potential addition to the standard of care in the treatment of glioblastoma multiforme (GBM). In the last decade or so various research groups have conducted phase I and II trials of DC-immunotherapy on patients with newly diagnosed (ND) and recurrent GBM and other high-grade gliomas in an attempt to improve the poor prognosis. Results show an increase in overall survival (OS), while vaccination-related side effects are invariably mild. Northwest Biotherapeutics, Inc., Bethesda, Maryland, U.S.A. (NWBT) developed the DCVax (R)-L vaccine as an adjunct to the treatment of GBM. It is currently under evaluation in a phase III trial in patients with ND-GBM, which is the only ongoing trial of its kind. In this review current data and perspectives of this product are examined.

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