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Is the blood–brain barrier really disrupted in all glioblastomas? A critical assessment of existing clinical data

Authors :
Debra H. Brinkmann
Jann N. Sarkaria
Leland S. Hu
Nathalie Y. R. Agar
Terence C. Burns
Paul D. Brown
Ian F. Parney
Janice K. Laramy
Timothy J. Kaufmann
Nadia N. Laack
Deanna H. Pafundi
Caterina Giannini
Kristin R. Swanson
Evanthia Galanis
Sani H. Kizilbash
William F. Elmquist
Jan C. Buckner
Sarkaria J.N.
Hu L.S.
Parney I.F.
Pafundi D.H.
Brinkmann D.H.
Laack N.N.
Giannini C.
Burns T.C.
Kizilbash S.H.
Laramy J.K.
Swanson K.R.
Kaufmann T.J.
Brown P.D.
Agar N.Y.R.
Galanis E.
Buckner J.C.
Elmquist W.F.
Source :
Neuro-Oncology. 20:184-191
Publication Year :
2017
Publisher :
Oxford University Press (OUP), 2017.

Abstract

The blood–brain barrier (BBB) excludes the vast majority of cancer therapeutics from normal brain. However, the importance of the BBB in limiting drug delivery and efficacy is controversial in high-grade brain tumors, such as glioblastoma (GBM). The accumulation of normally brain impenetrant radiographic contrast material in essentially all GBM has popularized a belief that the BBB is uniformly disrupted in all GBM patients so that consideration of drug distribution across the BBB is not relevant in designing therapies for GBM. However, contrary to this view, overwhelming clinical evidence demonstrates that there is also a clinically significant tumor burden with an intact BBB in all GBM, and there is little doubt that drugs with poor BBB permeability do not provide therapeutically effective drug exposures to this fraction of tumor cells. This review provides an overview of the clinical literature to support a central hypothesis: that all GBM patients have tumor regions with an intact BBB, and cure for GBM will only be possible if these regions of tumor are adequately treated.

Details

ISSN :
15235866 and 15228517
Volume :
20
Database :
OpenAIRE
Journal :
Neuro-Oncology
Accession number :
edsair.doi.dedup.....9dc6422db6a3041a44d6b87c2bf7d016
Full Text :
https://doi.org/10.1093/neuonc/nox175