Fractionated Gamma Knife radiosurgery for skull base meningiomas: a single-institution experience.

CBCT = cone-beam CT CTCAE = Common Terminology Criteria for Adverse Events GKRS = Gamma Knife radiosurgery Gamma Knife radiosurgery KPS = Karnofsky Performance Scale PLE = perilesional edema SBM = skull base meningioma fGKRS = fractionated Gamma Knife radiosurgery fractionated radiosurgery meningioma skull base

Journal

Neurosurgical focus
ISSN: 1092-0684
Titre abrégé: Neurosurg Focus
Pays: United States
ID NLM: 100896471

Informations de publication

Date de publication:
01 06 2019
Historique:
received: 31 01 2019
accepted: 28 03 2019
entrez: 2 6 2019
pubmed: 4 6 2019
medline: 28 8 2020
Statut: ppublish

Résumé

OBJECTIVEGamma Knife radiosurgery (GKRS) has been successfully used for the treatment of intracranial meningiomas given its steep dose gradients and high-dose conformality. However, treatment of skull base meningiomas (SBMs) may pose significant risk to adjacent radiation-sensitive structures such as the cranial nerves. Fractionated GKRS (fGKRS) may decrease this risk, but until recently it has not been practical with traditional pin-based systems. This study reports the authors' experience in treating SBMs with fGKRS, using a relocatable, noninvasive immobilization system.METHODSThe authors performed a retrospective review of all patients who underwent fGKRS for SBMs between 2013 and 2018 delivered using the Extend relocatable frame system or the Icon system. Patient demographics, pre- and post-GKRS tumor characteristics, perilesional edema, prior treatment details, and clinical symptoms were evaluated. Volumetric analysis of pre-GKRS, post-GKRS, and subsequent follow-up visits was performed.RESULTSTwenty-five patients met inclusion criteria. Nineteen patients were treated with the Icon system, and 6 patients were treated with the Extend system. The mean pre-fGKRS tumor volume was 7.62 cm3 (range 4.57-13.07 cm3). The median margin dose was 25 Gy delivered in 4 (8%) or 5 (92%) fractions. The median follow-up time was 12.4 months (range 4.7-17.4 months). Two patients (9%) experienced new-onset cranial neuropathy at the first follow-up. The mean postoperative tumor volume reduction was 15.9% with 6 patients (27%) experiencing improvement of cranial neuropathy at the first follow-up. Median first follow-up scans were obtained at 3.4 months (range 2.8-4.3 months). Three patients (12%) developed asymptomatic, mild perilesional edema by the first follow-up, which remained stable subsequently.CONCLUSIONSfGKRS with relocatable, noninvasive immobilization systems is well tolerated in patients with SBMs and demonstrated satisfactory tumor control as well as limited radiation toxicity. Future prospective studies with long-term follow-up and comparison to single-session GKRS or fractionated stereotactic radiotherapy are necessary to validate these findings and determine the efficacy of this approach in the management of SBMs.

Identifiants

pubmed: 31153152
doi: 10.3171/2019.3.FOCUS1963
pii: 2019.3.FOCUS1963
doi:
pii:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

E8

Auteurs

Krishna C Joshi (KC)

1Department of Neurosurgery, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University.
3Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center, Neurological Institute; and.

Alankrita Raghavan (A)

2Case Western Reserve University School of Medicine.

Baha'eddin Muhsen (B)

1Department of Neurosurgery, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University.
3Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center, Neurological Institute; and.

Jason Hsieh (J)

1Department of Neurosurgery, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University.

Hamid Borghei-Razavi (H)

1Department of Neurosurgery, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University.
3Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center, Neurological Institute; and.

Samuel T Chao (ST)

3Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center, Neurological Institute; and.
4Department of Radiation Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.

Gene H Barnett (GH)

1Department of Neurosurgery, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University.
3Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center, Neurological Institute; and.

John H Suh (JH)

3Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center, Neurological Institute; and.
4Department of Radiation Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.

Gennady Neyman (G)

3Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center, Neurological Institute; and.
4Department of Radiation Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.

Varun R Kshettry (VR)

1Department of Neurosurgery, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University.
3Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center, Neurological Institute; and.

Pablo F Recinos (PF)

1Department of Neurosurgery, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University.
3Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center, Neurological Institute; and.

Alireza M Mohammadi (AM)

1Department of Neurosurgery, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University.
3Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center, Neurological Institute; and.

Lilyana Angelov (L)

1Department of Neurosurgery, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University.
3Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center, Neurological Institute; and.

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