Gamma Knife Stereotactic Radiosurgery favorably changes the clinical course of hemangioblastoma growth in von Hippel-Lindau and sporadic patients.
Gamma Knife
Hemangioblastoma
Oncology
Sporadic
Stereotactic radiosurgery
Von Hippel-Lindau
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
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
471-478Subventions
Organisme : NCI NIH HHS
ID : P30 CA012197
Pays : United States
Organisme : Comprehensive Cancer Center at Wake Forest Baptist Medical Center
ID : P30 CA012197-40
Références
World Neurosurg. 2011 Jan;75(1):99-105; discussion 45-8
pubmed: 21492672
J Neurosurg. 2015 Mar;122(3):536-42
pubmed: 25555193
JAMA Neurol. 2018 May 1;75(5):620-627
pubmed: 29379961
J Neurosurg. 2005 Jan;102 Suppl:97-101
pubmed: 15662788
N Engl J Med. 1998 Nov 12;339(20):1426-33
pubmed: 9811917
Neurosurgery. 2001 Jan;48(1):55-62; discussion 62-3
pubmed: 11152361
J Neurooncol. 2012 May;108(1):179-85
pubmed: 22359231
J Clin Neurosci. 2016 Sep;31:147-51
pubmed: 27422585
J Clin Neurosci. 2011 Feb;18(2):171-80
pubmed: 21215639
J Neurosurg. 1991 Apr;74(4):552-9
pubmed: 2002367
Br J Neurosurg. 2004 Aug;18(4):338-42
pubmed: 15702831
Crit Rev Oncol Hematol. 2013 Apr;86(1):69-84
pubmed: 23148943
J Neurosurg. 2014 May;120(5):1055-62
pubmed: 24579662
Clin Transl Oncol. 2010 Mar;12(3):160-5
pubmed: 20231120
PLoS One. 2010 Aug 19;5(8):e12310
pubmed: 20808818
Neuro Oncol. 2014 Mar;16(3):429-33
pubmed: 24335701
J Neurosurg. 2015 Jun;122(6):1469-78
pubmed: 25816088
Front Mol Biosci. 2014 Nov 17;1:24
pubmed: 25988165