A Comparison of Clinical Outcomes for Subependymal Giant Cell Astrocytomas Treated with Laser Interstitial Thermal Therapy, Open Surgical Resection, and mTOR Inhibitors.

Astrocytoma Laser interstitial thermal therapy Pediatric neurosurgery Subependymal giant cell astrocytoma Tuberous sclerosis mTOR inhibitor

Journal

Pediatric neurosurgery
ISSN: 1423-0305
Titre abrégé: Pediatr Neurosurg
Pays: Switzerland
ID NLM: 9114967

Informations de publication

Date de publication:
2023
Historique:
received: 01 03 2022
accepted: 15 05 2023
medline: 31 8 2023
pubmed: 26 5 2023
entrez: 26 5 2023
Statut: ppublish

Résumé

Subependymal giant cell astrocytoma (SEGA) is the most common CNS tumor in patients with tuberous sclerosis complex (TSC). Although these are benign, their proximity to the foramen of Monroe frequently causes obstructive hydrocephalus, a potentially fatal complication. Open surgical resection has been the mainstay of treatment; however, this can cause significant morbidity. The development of mTOR inhibitors has changed the treatment landscape, but there are limitations to their use. Laser interstitial thermal therapy (LITT) is an emerging treatment modality that has shown promise in treatment of a variety of intracranial lesions, including SEGAs. We present a single institution, retrospective study of patients treated for SEGAs with LITT, open resection, mTOR inhibitors, or a combination of these modalities. The primary study outcome was tumor volume at most recent follow-up compared with volume at treatment initiation. The secondary outcome was clinical complications associated with treatment modality. Retrospective chart review was performed to identify patients with SEGAs treated at our institution from 2010 to 2021. Demographics, treatment information, and complications were collected from the medical record. Tumor volumes were calculated from imaging obtained at initiation of treatment and at most recent follow-up. Kruskal-Wallis nonparametric testing was used to assess differences in tumor volume and follow-up duration between groups. Four patients underwent LITT (3 with LITT only), three underwent open surgical resection, and four were treated with mTOR inhibitors only. Mean percent tumor volume reduction for each group was 48.6 ± 13.8, 90.7 ± 39.8, and 67.1 ± 17.2%, respectively. No statistically significant difference was identified comparing percent tumor volume reduction between the three groups (p = 0.0513). Additionally, there was no statistically significant difference in follow-up duration between groups (p = 0.223). Only 1 patient in our series required permanent CSF diversion and 4 discontinued or decreased the dose of mTOR inhibitor due to either cost or side effects. Our study suggests that LITT could be considered as a treatment option for SEGAs as it was effective in reducing tumor volume with very few complications. This modality is less invasive than open resection and may be an alternative for patients who are not candidates for mTOR inhibitors. We recommend an updated paradigm for SEGA treatment which includes LITT in select cases after consideration of patient-specific factors.

Identifiants

pubmed: 37232001
pii: 000531210
doi: 10.1159/000531210
doi:

Substances chimiques

MTOR Inhibitors 0

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

150-159

Informations de copyright

The Author(s). Published by S. Karger AG, Basel.

Auteurs

Scott Boop (S)

Department of Neurological Surgery, University of Washington, Seattle, Washington, USA.

David Bonda (D)

Department of Neurological Surgery, University of Washington, Seattle, Washington, USA.
Division of Neurosurgery, Seattle Children's Hospital, Seattle, Washington, USA.

Stephanie Randle (S)

Division of Pediatric Neurology, Department of Neurology, University of Washington, Seattle, Washington, USA.

Sarah Leary (S)

Division of Pediatric Neurology, Department of Neurology, University of Washington, Seattle, Washington, USA.

Nicholas Vitanza (N)

Division of Pediatric Neurology, Department of Neurology, University of Washington, Seattle, Washington, USA.
Division of Pediatric Hematology/Oncology, Department of Pediatrics, Seattle Children's, University of Washington, Fred Hutch Cancer Research Center, Seattle, Washington, USA.

Erin Crotty (E)

Division of Pediatric Neurology, Department of Neurology, University of Washington, Seattle, Washington, USA.

Edward Novotny (E)

Division of Pediatric Neurology, Department of Neurology, University of Washington, Seattle, Washington, USA.

Seth Friedman (S)

Department of Radiology, Seattle Children's Hospital, Seattle, Washington, USA.

Richard G Ellenbogen (RG)

Department of Neurological Surgery, University of Washington, Seattle, Washington, USA.
Division of Neurosurgery, Seattle Children's Hospital, Seattle, Washington, USA.

Sharon Durfy (S)

Department of Neurological Surgery, University of Washington, Seattle, Washington, USA.

Hannah Goldstein (H)

Department of Neurological Surgery, University of Washington, Seattle, Washington, USA.
Division of Neurosurgery, Seattle Children's Hospital, Seattle, Washington, USA.

Jeffrey G Ojemann (JG)

Department of Neurological Surgery, University of Washington, Seattle, Washington, USA.
Division of Neurosurgery, Seattle Children's Hospital, Seattle, Washington, USA.

Jason S Hauptman (JS)

Department of Neurological Surgery, University of Washington, Seattle, Washington, USA.
Division of Neurosurgery, Seattle Children's Hospital, Seattle, Washington, USA.

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