Unknown

Dataset Information

0

Prospective natural history study of central nervous system hemangioblastomas in von Hippel-Lindau disease.


ABSTRACT: OBJECT:The tumors most frequently associated with von Hippel-Lindau (VHL) disease are hemangioblastomas. While they are associated with significant neurological impairment and mortality, their natural history and optimal management have not been fully defined. METHODS:Patients with VHL were enrolled in a prospective study designed to define the natural history of CNS hemangioblastomas. In the present analysis, serial imaging, laboratory, genetic, and clinical data were evaluated in those with at least 2 years of follow-up data. RESULTS:At study entrance 225 patients (111 males, 114 females) harbored 1921 CNS hemangioblastomas in the supratentorial compartment (21 tumors [1%]), cerebellum (865 [45%]), brainstem (129 [7%]), spinal cord (689 [36%]), cauda equina (212 [11%]), and nerve roots (5 [0.3%]; follow-up 15,819 hemangioblastoma-years). Increased tumor burden was associated with partial deletions in the VHL gene (p = 0.005) and male sex (p = 0.002). Hemangioblastoma development (median 0.3 new tumors/year) was associated with younger age (p < 0.0001) and more tumors at study entrance (p < 0.0001). While 1278 hemangioblastomas (51%) did not grow, 1227 hemangioblastomas (49%) grew in a saltatory (886 [72%]), linear (76 [6%]), or exponential (264 [22%]) pattern. Faster tumor growth was associated with male sex (p = 0.001), symptomatic tumors (p < 0.0001), and tumors associated with cysts (p < 0.0001). Location-dependent tumor size was the primary predictor of eventual symptom formation (159 symptomatic tumors [6.3%]; area under the curve > 0.9). CONCLUSIONS:Central nervous system hemangioblastoma burden in VHL is associated with partial germline deletions and male sex. Unpredictable growth of hemangioblastomas compromises assessment of nonsurgical therapies. The judicious treatment of symptom-producing hemangioblastomas, while avoiding unnecessary treatment of asymptomatic tumors that may not progress, can provide clinical stability.

SUBMITTER: Lonser RR 

PROVIDER: S-EPMC4762041 | biostudies-literature | 2014 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

Prospective natural history study of central nervous system hemangioblastomas in von Hippel-Lindau disease.

Lonser Russell R RR   Butman John A JA   Huntoon Kristin K   Asthagiri Ashok R AR   Wu Tianxia T   Bakhtian Kamran D KD   Chew Emily Y EY   Zhuang Zhengping Z   Linehan W Marston WM   Oldfield Edward H EH  

Journal of neurosurgery 20140228 5


<h4>Object</h4>The tumors most frequently associated with von Hippel-Lindau (VHL) disease are hemangioblastomas. While they are associated with significant neurological impairment and mortality, their natural history and optimal management have not been fully defined.<h4>Methods</h4>Patients with VHL were enrolled in a prospective study designed to define the natural history of CNS hemangioblastomas. In the present analysis, serial imaging, laboratory, genetic, and clinical data were evaluated i  ...[more]

Similar Datasets

| S-EPMC5570160 | biostudies-literature
| S-EPMC7528461 | biostudies-literature
| S-EPMC8223245 | biostudies-literature
| S-EPMC7446124 | biostudies-literature
| S-EPMC4928600 | biostudies-literature
| S-EPMC7051770 | biostudies-literature
| S-EPMC5468534 | biostudies-other
| S-EPMC4896541 | biostudies-literature
| S-EPMC5066214 | biostudies-literature
| S-EPMC5240113 | biostudies-literature