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

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