Stereotactic Radiosurgery for Intracranial Ependymomas: An International Multicenter Study.


Journal

Neurosurgery
ISSN: 1524-4040
Titre abrégé: Neurosurgery
Pays: United States
ID NLM: 7802914

Informations de publication

Date de publication:
01 01 2019
Historique:
received: 17 11 2017
accepted: 18 02 2018
pubmed: 3 4 2018
medline: 3 1 2020
entrez: 3 4 2018
Statut: ppublish

Résumé

Stereotactic radiosurgery (SRS) is a potentially important option for intracranial ependymoma patients. To analyze the outcomes of intracranial ependymoma patients who underwent SRS as a part of multimodality management. Seven centers participating in the International Gamma Knife Research Foundation identified 89 intracranial ependymoma patients who underwent SRS (113 tumors). The median patient age was 16.3 yr (2.9-80). All patients underwent previous surgical resection and radiation therapy (RT) of their ependymomas and 40 underwent previous chemotherapy. Grade 2 ependymomas were present in 42 patients (52 tumors) and grade 3 ependymomas in 48 patients (61 tumors). The median tumor volume was 2.2 cc (0.03-36.8) and the median margin dose was 15 Gy (9-24). Forty-seven (53%) patients were alive and 42 (47%) patients died at the last follow-up. The overall survival after SRS was 86% at 1 yr, 50% at 3 yr, and 44% at 5 yr. Smaller total tumor volume was associated with longer overall survival (P = .006). Twenty-two patients (grade 2: n = 9, grade 3: n = 13) developed additional recurrent ependymomas in the craniospinal axis. The progression-free survival after SRS was 71% at 1 yr, 56% at 3 yr, and 48% at 5 yr. Adult age, female sex, and smaller tumor volume indicated significantly better progression-free survival. Symptomatic adverse radiation effects were seen in 7 patients (8%). SRS provides another management option for residual or recurrent progressive intracranial ependymoma patients who have failed initial surgery and RT.

Sections du résumé

BACKGROUND
Stereotactic radiosurgery (SRS) is a potentially important option for intracranial ependymoma patients.
OBJECTIVE
To analyze the outcomes of intracranial ependymoma patients who underwent SRS as a part of multimodality management.
METHODS
Seven centers participating in the International Gamma Knife Research Foundation identified 89 intracranial ependymoma patients who underwent SRS (113 tumors). The median patient age was 16.3 yr (2.9-80). All patients underwent previous surgical resection and radiation therapy (RT) of their ependymomas and 40 underwent previous chemotherapy. Grade 2 ependymomas were present in 42 patients (52 tumors) and grade 3 ependymomas in 48 patients (61 tumors). The median tumor volume was 2.2 cc (0.03-36.8) and the median margin dose was 15 Gy (9-24).
RESULTS
Forty-seven (53%) patients were alive and 42 (47%) patients died at the last follow-up. The overall survival after SRS was 86% at 1 yr, 50% at 3 yr, and 44% at 5 yr. Smaller total tumor volume was associated with longer overall survival (P = .006). Twenty-two patients (grade 2: n = 9, grade 3: n = 13) developed additional recurrent ependymomas in the craniospinal axis. The progression-free survival after SRS was 71% at 1 yr, 56% at 3 yr, and 48% at 5 yr. Adult age, female sex, and smaller tumor volume indicated significantly better progression-free survival. Symptomatic adverse radiation effects were seen in 7 patients (8%).
CONCLUSION
SRS provides another management option for residual or recurrent progressive intracranial ependymoma patients who have failed initial surgery and RT.

Identifiants

pubmed: 29608701
pii: 4955825
doi: 10.1093/neuros/nyy082
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

227-234

Auteurs

Hideyuki Kano (H)

Department of Neurological Surgery, Center for Image-Guided Neurosurgery, University of Pittsburgh, Pittsburgh, Pennsylvania.

Yan-Hua Su (YH)

Department of Neurosurgery, Taipei Veteran General Hospital, Taipei, Taiwan.

Hsiu-Mei Wu (HM)

Department of Neurosurgery, Taipei Veteran General Hospital, Taipei, Taiwan.

Gabriela Simonova (G)

Stereotactic and Radiation Neurosurgery, Na Homolce Hospital, Prague, Czech.

Roman Liscak (R)

Stereotactic and Radiation Neurosurgery, Na Homolce Hospital, Prague, Czech.

Or Cohen-Inbar (O)

Department of Neurosurgery, University of Virginia, Charlottesville, Virginia.

Jason P Sheehan (JP)

Department of Neurosurgery, University of Virginia, Charlottesville, Virginia.

Antonio Meola (A)

Department of Neurosurgery, Cleveland Clinic Foundation, Cleveland, Ohio.

Mayur Sharma (M)

Department of Neurosurgery, Cleveland Clinic Foundation, Cleveland, Ohio.

Gene H Barnett (GH)

Department of Neurosurgery, Cleveland Clinic Foundation, Cleveland, Ohio.

David Mathieu (D)

Division of Neurosurgery, Université de Sherbrooke, Centre de Recherche du CHUS, Sherbrooke, Canada.

Lucas T Vasas (LT)

Section of Neurosurgery, University of Manitoba, Canada.

Anthony M Kaufmann (AM)

Section of Neurosurgery, University of Manitoba, Canada.

Rachel C Jacobs (RC)

Department of Neurological Surgery, Center for Image-Guided Neurosurgery, University of Pittsburgh, Pittsburgh, Pennsylvania.

L Dade Lunsford (LD)

Department of Neurological Surgery, Center for Image-Guided Neurosurgery, University of Pittsburgh, Pittsburgh, Pennsylvania.

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