Resection extent and BRAF V600E mutation status determine postoperative tumor growth velocity in pediatric low-grade glioma: results from a single-center cohort analysis.


Journal

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

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 18 07 2022
accepted: 18 10 2022
pubmed: 3 11 2022
medline: 21 12 2022
entrez: 2 11 2022
Statut: ppublish

Résumé

Despite excellent long-term overall survival rates, pediatric low-grade gliomas (pLGG) show high variety of clinical behavior regarding progress or senescence post incomplete resection (IR). This study retrospectively analyzes tumor growth velocity (TGV) of pLGG before surgery and after IR to investigate the impact of surgical extent, tumor location and molecular BRAF status on postoperative residual tumor growth behavior. Of a total of 172 patients with pLGG receiving surgical treatment, 107 underwent IR (66%). Fifty-three vs 94 patients could be included in the pre- and post-operative cohort, respectively, and were observed over a mean follow-up time of 40.2 vs 60.1 months. Sequential three-dimensional MRI-based tumor volumetry of a total of 407 MRI scans was performed to calculate pre- and postoperative TGV. Mean preoperative TGV of 0.264 cm This data suggests that extensive surgical resection may impact pediatric LGG growth kinetics post incomplete resection by inducing a significant deceleration of tumor growth. BRAF-V600E mutation may be a risk factor for higher postoperative TGV.

Identifiants

pubmed: 36319795
doi: 10.1007/s11060-022-04176-4
pii: 10.1007/s11060-022-04176-4
pmc: PMC9758245
doi:

Substances chimiques

Proto-Oncogene Proteins B-raf EC 2.7.11.1
BRAF protein, human EC 2.7.11.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

567-576

Informations de copyright

© 2022. The Author(s).

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Auteurs

David Gorodezki (D)

Department of Hematology and Oncology, University Children's Hospital Tübingen, Tübingen, Germany. david.gorodezki@med.uni-tuebingen.de.

Julian Zipfel (J)

Section of Pediatric Neurosurgery, Department of Neurosurgery, University Hospital Tübingen, Tübingen, Germany.

Manon Queudeville (M)

Department of Hematology and Oncology, University Children's Hospital Tübingen, Tübingen, Germany.
Clinic for Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Jordana Sosa (J)

Section of Pediatric Neurosurgery, Department of Neurosurgery, University Hospital Tübingen, Tübingen, Germany.

Ursula Holzer (U)

Department of Hematology and Oncology, University Children's Hospital Tübingen, Tübingen, Germany.

Jan Kern (J)

Department of Neuropediatrics and Developmental Neurology, University Hospital Tübingen, Tübingen, Germany.

Andrea Bevot (A)

Department of Neuropediatrics and Developmental Neurology, University Hospital Tübingen, Tübingen, Germany.

Jens Schittenhelm (J)

Department of Neuropathology, Institute of Pathology, University Hospital Tübingen, Tübingen, Germany.

Thomas Nägele (T)

Department of Neuroradiology, University Hospital Tübingen, Tübingen, Germany.

Martin Ebinger (M)

Department of Hematology and Oncology, University Children's Hospital Tübingen, Tübingen, Germany.

Martin U Schuhmann (MU)

Section of Pediatric Neurosurgery, Department of Neurosurgery, University Hospital Tübingen, Tübingen, Germany.

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