Stereotactic Radiosurgery for Intracranial Ependymomas: An International Multicenter Study.
Adolescent
Adult
Aged
Aged, 80 and over
Brain Neoplasms
/ mortality
Child
Child, Preschool
Combined Modality Therapy
/ methods
Disease Progression
Ependymoma
/ mortality
Female
Humans
Male
Middle Aged
Neoplasm Recurrence, Local
/ mortality
Progression-Free Survival
Radiosurgery
/ adverse effects
Retrospective Studies
Treatment Outcome
Young Adult
Journal
Neurosurgery
ISSN: 1524-4040
Titre abrégé: Neurosurgery
Pays: United States
ID NLM: 7802914
Informations de publication
Date de publication:
01 01 2019
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