Surgical management of lower-grade glioma in the spotlight of the 2016 WHO classification system.


Journal

Journal of neuro-oncology
ISSN: 1573-7373
Titre abrégé: J Neurooncol
Pays: United States
ID NLM: 8309335

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 29 07 2018
accepted: 07 10 2018
pubmed: 24 11 2018
medline: 16 4 2019
entrez: 24 11 2018
Statut: ppublish

Résumé

According to the 2016 WHO classification lower-grade gliomas consist of three groups: IDH-mutated and 1p/19q co-deleted, IDH-mutated and IDH-wildtype tumors. The aim of this study was to evaluate the impact of surgical therapy for lower-grade gliomas with a particular focus on the molecular subgroups. This is a bi-centric retrospective analysis including 299 patients, who underwent treatment for lower-grade glioma between 1990 and 2016. All tumors were re-classified according to the 2016 WHO classification. Data concerning baseline and tumor characteristics, overall survival, different treatment modalities and functional outcome were analyzed. A total of 112 (37.5%) patients with IDH-mutation and 1p/19q co-deletetion, 86 (28.8%) patients with IDH-mutation and 101 (33.8%) patients with IDH-wildtype tumors were identified. The median overall survival (mOS) differed significantly between the groups (p < 0.001). Surgical resection was performed in 226 patients and showed significantly improved mOS compared to the biopsy group (p = 0.001). Gross total resection (GTR) was associated with better survival (p = 0.007) in the whole cohort as well as in the IDH-mutated and IDH-wildtype groups compared to partial resection or biopsy. IDH-wildtype patients presented a significant survival benefit after combined radio-chemotherapy compared to radio- or chemotherapy alone (p = 0.02). Good clinical status (NANO) was associated with longer OS (p = 0.001). The impact of surgical treatment on the outcome of lower-grade gliomas depends to a great extent on the molecular subtype of the tumors. Patients with more aggressive tumors (IDH-wildtype) seem to profit from more intensive treatment like GTR, multiple resections and combined radio-/chemotherapy.

Identifiants

pubmed: 30467813
doi: 10.1007/s11060-018-03030-w
pii: 10.1007/s11060-018-03030-w
doi:

Substances chimiques

IDH2 protein, human EC 1.1.1.41
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

223-233

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Auteurs

Daniel Delev (D)

Department of Neurosurgery, Medical Center, Freiburg, Germany. delev.daniel@gmail.com.
Medical Faculty, Freiburg University, Freiburg, Germany. delev.daniel@gmail.com.

Dieter Henrik Heiland (DH)

Department of Neurosurgery, Medical Center, Freiburg, Germany.
Medical Faculty, Freiburg University, Freiburg, Germany.

Pamela Franco (P)

Department of Neurosurgery, Medical Center, Freiburg, Germany.
Medical Faculty, Freiburg University, Freiburg, Germany.

Peter Reinacher (P)

Department of Stereotactic and Functional Neurosurgery, Medical Center, Freiburg, Germany.
Medical Faculty, Freiburg University, Freiburg, Germany.

Irina Mader (I)

Department of Neuroradiology, Medical Center, Freiburg, Germany.
Medical Faculty, Freiburg University, Freiburg, Germany.

Ori Staszewski (O)

Institute of Neuropathology, Freiburg University Medical Center, Freiburg, Germany.
Medical Faculty, Freiburg University, Freiburg, Germany.

Silke Lassmann (S)

Institute of Pathology, University of Freiburg, Freiburg, Germany.
Medical Faculty, Freiburg University, Freiburg, Germany.

Stefan Grau (S)

Department of Neurosurgery, University Hospital Cologne, Cologne, Germany.

Oliver Schnell (O)

Department of Neurosurgery, Medical Center, Freiburg, Germany.
Medical Faculty, Freiburg University, Freiburg, Germany.

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