Long‐term efficacy and toxicity of bevacizumab‐based therapy in children with recurrent low‐grade gliomas
Male
Brain Neoplasms
Infant
Angiogenesis Inhibitors
Glioma
Antibodies, Monoclonal, Humanized
3. Good health
Bevacizumab
03 medical and health sciences
Treatment Outcome
0302 clinical medicine
Child, Preschool
Humans
Female
Neoplasm Recurrence, Local
Child
Retrospective Studies
DOI:
10.1002/pbc.24297
Publication Date:
2012-09-13T16:26:45Z
AUTHORS (8)
ABSTRACT
Because definitive resection or radiotherapy for pediatric low-grade gliomas (LGGs) may be associated with severe and permanent adverse effects, medical management has taken a significant role. Bevacizumab-based therapy demonstrated encouraging responses; however, longer-term toxicity, response durability alternative dosing regimens have not been evaluated.This was retrospective review of children multiply recurrent, progressive LGGs treated bevacizumab-based followed at least 12 months after treatment completion. Toxicity uniformly graded imaging centrally reviewed.All fourteen patients had failed two prior regimens; six dissemination. Patients received initial median age 5.3 years (range, 1-12 years). Median duration 1-24 months). an objective response; 2 stable disease. time to maximum 9 weeks 7-17 weeks). No progressed on therapy, although 13/14 stopping bevacizumab 5 months. Four were re-treated all again responded stabilized. Alternative strategies effective, including monotherapy prolonging the interval 3 weeks. High-grade bevacizumab-related toxicities consisted grade proteinuria (n = 2), primary inflammatory arthritis 1), somnolence 1). Toxicities resolved within 6 cessation except one case hypertension.Bevacizumab-based is successful inducing rapid LGG response. progressing off-therapy successfully bevacizumab. Nearly tumors progress once discontinued. are insignificant but usually reversible.
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