Treatment Outcomes and Dose Rate Effects Following Gamma Knife Stereotactic Radiosurgery for Vestibular Schwannomas.


Journal

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

Informations de publication

Date de publication:
01 12 2019
Historique:
received: 12 09 2018
accepted: 08 03 2019
pubmed: 5 7 2019
medline: 14 4 2020
entrez: 5 7 2019
Statut: ppublish

Résumé

Gamma Knife radiosurgery (GKRS; Elekta AB) remains a well-established treatment modality for vestibular schwannomas. Despite highly effective tumor control, further research is needed toward optimizing long-term functional outcomes. Whereas dose-rate effects may impact post-treatment toxicities given tissue dose-response relationships, potential effects remain largely unexplored. To evaluate treatment outcomes and potential dose-rate effects following definitive GKRS for vestibular schwannomas. We retrospectively reviewed 419 patients treated at our institution between 1998 and 2015, characterizing baseline demographics, pretreatment symptoms, and GKRS parameters. The cohort was divided into 2 dose-rate groups based on the median value (2.675 Gy/min). Outcomes included clinical tumor control, radiographic progression-free survival, serviceable hearing preservation, hearing loss, and facial nerve dysfunction (FND). Prognostic factors were assessed using Cox regression. The study cohort included 227 patients with available follow-up. Following GKRS 2-yr and 4-yr clinical tumor control rates were 98% (95% CI: 95.6%-100%) and 96% (95% CI: 91.4%-99.6%), respectively. Among 177 patients with available radiographic follow-up, 2-yr and 4-yr radiographic progression-free survival rates were 97% (95% CI: 94.0%-100.0%) and 88% (95% CI: 81.2%-95.0%). The serviceable hearing preservation rate was 72.2% among patients with baseline Gardner-Robertson class I/II hearing and post-treatment audiological evaluations. Most patients experienced effective relief from prior headaches (94.7%), tinnitus (83.7%), balance issues (62.7%), FND (90.0%), and trigeminal nerve dysfunction (79.2%), but not hearing loss (1.0%). Whereas GKRS provided effective tumor control independently of dose rate, GKRS patients exposed to lower dose rates experienced significantly better freedom from post-treatment hearing loss and FND (P = .044). Whereas GKRS provides excellent tumor control and effective symptomatic relief for vestibular schwannomas, dose-rate effects may impact post-treatment functional outcomes. Further research remains warranted.

Sections du résumé

BACKGROUND
Gamma Knife radiosurgery (GKRS; Elekta AB) remains a well-established treatment modality for vestibular schwannomas. Despite highly effective tumor control, further research is needed toward optimizing long-term functional outcomes. Whereas dose-rate effects may impact post-treatment toxicities given tissue dose-response relationships, potential effects remain largely unexplored.
OBJECTIVE
To evaluate treatment outcomes and potential dose-rate effects following definitive GKRS for vestibular schwannomas.
METHODS
We retrospectively reviewed 419 patients treated at our institution between 1998 and 2015, characterizing baseline demographics, pretreatment symptoms, and GKRS parameters. The cohort was divided into 2 dose-rate groups based on the median value (2.675 Gy/min). Outcomes included clinical tumor control, radiographic progression-free survival, serviceable hearing preservation, hearing loss, and facial nerve dysfunction (FND). Prognostic factors were assessed using Cox regression.
RESULTS
The study cohort included 227 patients with available follow-up. Following GKRS 2-yr and 4-yr clinical tumor control rates were 98% (95% CI: 95.6%-100%) and 96% (95% CI: 91.4%-99.6%), respectively. Among 177 patients with available radiographic follow-up, 2-yr and 4-yr radiographic progression-free survival rates were 97% (95% CI: 94.0%-100.0%) and 88% (95% CI: 81.2%-95.0%). The serviceable hearing preservation rate was 72.2% among patients with baseline Gardner-Robertson class I/II hearing and post-treatment audiological evaluations. Most patients experienced effective relief from prior headaches (94.7%), tinnitus (83.7%), balance issues (62.7%), FND (90.0%), and trigeminal nerve dysfunction (79.2%), but not hearing loss (1.0%). Whereas GKRS provided effective tumor control independently of dose rate, GKRS patients exposed to lower dose rates experienced significantly better freedom from post-treatment hearing loss and FND (P = .044).
CONCLUSION
Whereas GKRS provides excellent tumor control and effective symptomatic relief for vestibular schwannomas, dose-rate effects may impact post-treatment functional outcomes. Further research remains warranted.

Identifiants

pubmed: 31270543
pii: 5528101
doi: 10.1093/neuros/nyz229
pmc: PMC6855984
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

E1084-E1094

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© Congress of Neurological Surgeons 2019.

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Auteurs

Deborah Ruth Smith (DR)

Department of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.

Heva Jasmine Saadatmand (HJ)

Department of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.

Cheng-Chia Wu (CC)

Department of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.

Paul J Black (PJ)

Department of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.

Yen-Ruh Wuu (YR)

Department of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.

Jeraldine Lesser (J)

Department of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.

Maryellen Horan (M)

Department of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.

Steven R Isaacson (SR)

Department of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.

Tony J C Wang (TJC)

Department of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.
Department of Neurological Surgery, Columbia University Irving Medical Center, New York, New York.
Herbert Irving Comprehensive Cancer Center, NewYork-Presbyterian/Columbia University Irving Medical Center, New York, New York.

Michael B Sisti (MB)

Department of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.
Department of Neurological Surgery, Columbia University Irving Medical Center, New York, New York.
Herbert Irving Comprehensive Cancer Center, NewYork-Presbyterian/Columbia University Irving Medical Center, New York, New York.
Department of Otolaryngology: Head and Neck Surgery, Columbia University Irving Medical Center, New York, New York.

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