Dissemination Patterns and Short-Term Management of Multifocal Rosette-Forming Glioneuronal Tumors.


Journal

World neurosurgery
ISSN: 1878-8769
Titre abrégé: World Neurosurg
Pays: United States
ID NLM: 101528275

Informations de publication

Date de publication:
05 2021
Historique:
received: 16 12 2020
revised: 09 02 2021
accepted: 10 02 2021
pubmed: 22 2 2021
medline: 4 8 2021
entrez: 21 2 2021
Statut: ppublish

Résumé

Multifocal rosette-forming glioneuronal tumors (RGNTs) are challenging to manage. Gross total resection is often impossible, and data on adjunctive therapies are limited. We reviewed cases of multifocal RGNTs in the literature with special focus on dissemination patterns and management. A literature review was conducted using PubMed and the key words "(multifocal OR multicentric OR satellite OR dissemination) AND glioneuronal." There were 21 cases of multifocal RGNTs identified. Follow-up was available in 18 cases at a median of 17 months. Progression-free survival and overall survival at 1 year were 84% and 94%, respectively. Of all cases, 43% had cerebrospinal fluid (CSF) dissemination, 48% had intraparenchymal spread, and 10% had both. The presence of CSF dissemination led to palliative care and/or death in 20% of cases (n = 2). None of the cases with intraparenchymal spread progressed. Radiotherapy was used in 50% of cases with CSF dissemination, chemotherapy was used in 20%, and CSF shunting was used in 36%. No tumors with intraparenchymal spread required adjunctive therapy or shunting. RGNTs with CSF dissemination are more likely to behave aggressively, and early adjunctive therapies should be discussed with patients. Tumors with intraparenchymal spread grow slowly, and maximal safe resection followed by observation is likely sufficient in the short term. Long-term behavior of multifocal RGNTs is still unclear.

Sections du résumé

BACKGROUND
Multifocal rosette-forming glioneuronal tumors (RGNTs) are challenging to manage. Gross total resection is often impossible, and data on adjunctive therapies are limited. We reviewed cases of multifocal RGNTs in the literature with special focus on dissemination patterns and management.
METHODS
A literature review was conducted using PubMed and the key words "(multifocal OR multicentric OR satellite OR dissemination) AND glioneuronal."
RESULTS
There were 21 cases of multifocal RGNTs identified. Follow-up was available in 18 cases at a median of 17 months. Progression-free survival and overall survival at 1 year were 84% and 94%, respectively. Of all cases, 43% had cerebrospinal fluid (CSF) dissemination, 48% had intraparenchymal spread, and 10% had both. The presence of CSF dissemination led to palliative care and/or death in 20% of cases (n = 2). None of the cases with intraparenchymal spread progressed. Radiotherapy was used in 50% of cases with CSF dissemination, chemotherapy was used in 20%, and CSF shunting was used in 36%. No tumors with intraparenchymal spread required adjunctive therapy or shunting.
CONCLUSIONS
RGNTs with CSF dissemination are more likely to behave aggressively, and early adjunctive therapies should be discussed with patients. Tumors with intraparenchymal spread grow slowly, and maximal safe resection followed by observation is likely sufficient in the short term. Long-term behavior of multifocal RGNTs is still unclear.

Identifiants

pubmed: 33610864
pii: S1878-8750(21)00235-7
doi: 10.1016/j.wneu.2021.02.043
pii:
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

86-93

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Jakob T Hockman (JT)

Department of Neurosurgery, Saint Louis University School of Medicine, St. Louis, Missouri, USA; Department of Pathology, Saint Louis University School of Medicine, St. Louis, Missouri, USA.

Najib E El Tecle (NE)

Department of Neurosurgery, Saint Louis University School of Medicine, St. Louis, Missouri, USA. Electronic address: najib.eltecle@health.slu.edu.

Jorge F Urquiaga (JF)

Department of Neurosurgery, Saint Louis University School of Medicine, St. Louis, Missouri, USA.

Georgios Alexopoulos (G)

Department of Neurosurgery, Saint Louis University School of Medicine, St. Louis, Missouri, USA.

Miguel A Guzman (MA)

Department of Pathology, Saint Louis University School of Medicine, St. Louis, Missouri, USA.

Jeroen Coppens (J)

Department of Neurosurgery, Saint Louis University School of Medicine, St. Louis, Missouri, USA.

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