Bevacizumab as a surgery-sparing agent for spinal ependymoma in patients with neurofibromatosis type II: Systematic review and case
Document Type
Article
Abstract
Neurofibromatosis type 2 (NF2) is a rare, hereditary tumor syndrome, often requiring repeated surgeries for multiple lesions with significant cumulative morbidity. As such, non-operative management should be considered when possible for this patient population. The aim of this study is to provide a systematic review of the literature regarding this treatment strategy. A descriptive case of a patient in whom bevacizumab treatments enabled over 15 years of surgical postponement for a symptomatic spinal cord ependymoma is also provided. Evidence suggests that bevacizumab is a reasonable surgery-deferring option for cystic lesions, and it may be especially useful in NF2 patients to reduce cumulative morbidity.
Medical Subject Headings
Adult; Antineoplastic Agents, Immunological (therapeutic use); Bevacizumab (therapeutic use); Conservative Treatment (methods, trends); Ependymoma (complications, diagnostic imaging, drug therapy); Female; Humans; Neurofibromatosis 2 (complications, diagnostic imaging, drug therapy); Spinal Cord Neoplasms (complications, diagnostic imaging, drug therapy)
Publication Date
4-1-2021
Publication Title
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
E-ISSN
1532-2653
Volume
86
First Page
79
Last Page
84
PubMed ID
33775351
Digital Object Identifier (DOI)
10.1016/j.jocn.2021.01.010
Recommended Citation
Snyder, M Harrison; Ampie, Leonel; DiDomenico, Joseph D.; and Asthagiri, Ashok R., "Bevacizumab as a surgery-sparing agent for spinal ependymoma in patients with neurofibromatosis type II: Systematic review and case" (2021). Neurosurgery. 2165.
https://scholar.barrowneuro.org/neurosurgery/2165