Gamma Knife Stereotactic Radiosurgery favorably changes the clinical course of hemangioblastoma growth in von Hippel-Lindau and sporadic patients.


Journal

Journal of neuro-oncology
ISSN: 1573-7373
Titre abrégé: J Neurooncol
Pays: United States
ID NLM: 8309335

Informations de publication

Date de publication:
May 2019
Historique:
received: 06 11 2018
accepted: 01 02 2019
pubmed: 8 2 2019
medline: 30 8 2019
entrez: 8 2 2019
Statut: ppublish

Résumé

This is the first single-institution study of its size to characterize the treatment impact and to address the question of whether hemangioblastoma treatment with Gamma Knife Stereotactic Radiosurgery (GKRS) in both sporadic and VHL patients changes the characteristic saltatory hemangioblastoma growth pattern. The authors reviewed a single-institution tumor registry to identify patients who had received GKRS for hemangioblastomas between January 1st, 1999, and December 31st, 2017. 15 patients with 101 lesions met search criteria with a median age of first GKRS of 39.2 years (interquartile range [IQR] of 25.7-57.4 years), including 96 VHL and 5 sporadic lesions. The median time from GKRS to last follow-up was 5.4 years (IQR 2.3-11.5 years). 4 lesions (4%) and 3 patients (20%) experienced a local failure. The 1-year, 3-year, and 5-year freedom from new hemangioblastoma formation rates were 97%, 80%, and 46% respectively. Multivariate analysis revealed a reduction in tumor volume after GKRS. Several variables associated with a greater percent reduction in volume from GKRS to last follow-up: non-cystic status (p = .01), no prior craniotomy (p = .04), and follow-up time from GKRS (p < .0001). GKRS is a successful long-term treatment option for hemangioblastomas changing the clinical course from saltatory growth to reduction in tumor volume. Non-cystic tumors and those without prior craniotomy were associated with a greater percent reduction in volume from GKRS at last follow-up.

Identifiants

pubmed: 30729402
doi: 10.1007/s11060-019-03118-x
pii: 10.1007/s11060-019-03118-x
pmc: PMC6805133
mid: NIHMS1051014
doi:

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

471-478

Subventions

Organisme : NCI NIH HHS
ID : P30 CA012197
Pays : United States
Organisme : Comprehensive Cancer Center at Wake Forest Baptist Medical Center
ID : P30 CA012197-40

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Auteurs

Brittany Liebenow (B)

Departments of Neurosurgery, Wake Forest School of Medicine, Medical Center Blvd, Winston-Salem, NC, 27157, USA. bliebeno@wakehealth.edu.

Abigail Tatter (A)

Departments of Neurosurgery, Wake Forest School of Medicine, Medical Center Blvd, Winston-Salem, NC, 27157, USA.

William A Dezarn (WA)

Radiation Oncology, Wake Forest School of Medicine, Winston-Salem, NC, USA.

Scott Isom (S)

Biostatistical Sciences, Wake Forest School of Medicine, Winston-Salem, NC, USA.

Michael D Chan (MD)

Radiation Oncology, Wake Forest School of Medicine, Winston-Salem, NC, USA.

Stephen B Tatter (SB)

Departments of Neurosurgery, Wake Forest School of Medicine, Medical Center Blvd, Winston-Salem, NC, 27157, USA.

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Classifications MeSH