Association of Isocitrate Dehydrogenase (IDH) Status With Edema to Tumor Ratio and Its Correlation With Immune Infiltration in Glioblastoma.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2021
Historique:
received: 09 11 2020
accepted: 09 03 2021
entrez: 19 4 2021
pubmed: 20 4 2021
medline: 16 9 2021
Statut: epublish

Résumé

The extent of preoperative peritumoral edema in glioblastoma (GBM) has been negatively correlated with patient outcome. As several ongoing studies are investigating T-cell based immunotherapy in GBM, we conducted this study to assess whether peritumoral edema with potentially increased intracranial pressure, disrupted tissue homeostasis and reduced local blood flow has influence on immune infiltration and affects survival. A volumetric analysis of preoperative imaging (gadolinium enhanced T1 weighted MRI sequences for tumor size and T2 weighted sequences for extent of edema (including the infiltrative zone, gliosis etc.) was conducted in 144 patients using the Brainlab® software. Immunohistochemical staining was analyzed for lymphocytic- (CD 3+) and myelocytic (CD15+) tumor infiltration. A retrospective analysis of patient-, surgical-, and molecular characteristics was performed using medical records. The edema to tumor ratio was neither associated with progression-free nor overall survival (p=0.90, p=0.74). However, GBM patients displaying IDH-1 wildtype had significantly higher edema to tumor ratio than patients displaying an IDH-1 mutation (p=0.01). Immunohistopathological analysis did not show significant differences in lymphocytic or myelocytic tumor infiltration (p=0.78, p=0.74) between these groups. In our cohort, edema to tumor ratio had no significant correlation with immune infiltration and outcome. However, patients with an IDH-1wildtype GBM had a significantly higher edema to tumor ratio compared to their IDH-1 mutated peer group. Further studies are necessary to elucidate the underlying mechanisms.

Identifiants

pubmed: 33868245
doi: 10.3389/fimmu.2021.627650
pmc: PMC8044904
doi:

Substances chimiques

Biomarkers, Tumor 0
Isocitrate Dehydrogenase EC 1.1.1.41
IDH1 protein, human EC 1.1.1.42.

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

627650

Informations de copyright

Copyright © 2021 Dubinski, Won, Rauch, Behmanesh, Ngassam, Baumgarten, Senft, Harter, Bernstock, Freiman, Seifert and Gessler.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Daniel Dubinski (D)

Department of Neurosurgery, Goethe University Hospital, Frankfurt, Germany.

Sae-Yeon Won (SY)

Department of Neurosurgery, Goethe University Hospital, Frankfurt, Germany.

Maximilian Rauch (M)

Institute of Neuroradiology, Goethe University, Frankfurt, Germany.

Bedjan Behmanesh (B)

Department of Neurosurgery, Goethe University Hospital, Frankfurt, Germany.

Lionel D C Ngassam (LDC)

Department of Neurosurgery, Goethe University Hospital, Frankfurt, Germany.

Peter Baumgarten (P)

Department of Neurosurgery, Goethe University Hospital, Frankfurt, Germany.

Christian Senft (C)

Department of Neurosurgery, Goethe University Hospital, Frankfurt, Germany.

Patrick N Harter (PN)

Neurological Institute (Edinger Institute), Goethe University, Frankfurt, Germany.

Joshua D Bernstock (JD)

Department of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.

Thomas M Freiman (TM)

Department of Neurosurgery, Goethe University Hospital, Frankfurt, Germany.

Volker Seifert (V)

Department of Neurosurgery, Goethe University Hospital, Frankfurt, Germany.

Florian Gessler (F)

Department of Neurosurgery, Goethe University Hospital, Frankfurt, Germany.

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