Long-term efficacy and toxicity of bevacizumab-based therapy in children with recurrent low-grade gliomas

被引:95
作者
Hwang, Eugene I. [1 ,2 ,3 ]
Jakacki, Regina I. [4 ]
Fisher, Michael J. [5 ]
Kilburn, Lindsay B. [1 ,2 ,3 ]
Horn, Marianna [6 ]
Vezina, Gilbert [7 ]
Rood, Brian R. [1 ,2 ,3 ]
Packer, Roger J. [2 ,8 ,9 ]
机构
[1] Childrens Natl Med Ctr, Div Oncol, Ctr Canc & Blood Disorders, Washington, DC 20010 USA
[2] Childrens Natl Med Ctr, Brain Tumor Inst, Washington, DC 20010 USA
[3] George Washington Univ, Sch Med, Washington, DC USA
[4] Childrens Hosp Pittsburgh, Div Hematol Oncol, Pittsburgh, PA 15213 USA
[5] Childrens Hosp Pittsburgh, Div Oncol, Philadelphia, PA USA
[6] Childrens Ctr Canc & Blood Disorders Northern Vir, Falls Church, VA USA
[7] Childrens Natl Med Ctr, Dept Radiol, Washington, DC 20010 USA
[8] Childrens Natl Med Ctr, Ctr Neurosci & Behav Med, Washington, DC 20010 USA
[9] Childrens Natl Med Ctr, Gilbert Family NF Inst, Washington, DC 20010 USA
关键词
bevacizumab; gliomas; low-grade; pediatric; treatment; PEDIATRIC-PATIENTS; ONCOLOGY GROUP; TUMORS; ASTROCYTOMAS; TEMOZOLOMIDE; IRINOTECAN;
D O I
10.1002/pbc.24297
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background 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 has demonstrated encouraging responses; however, longer-term toxicity, response durability and alternative dosing regimens have not been evaluated. Procedure This was a retrospective review of children with multiply recurrent, progressive LGGs treated with bevacizumab-based therapy and followed for at least 12 months after treatment completion. Toxicity was uniformly graded and imaging was centrally reviewed. Results All fourteen patients had failed at least two prior treatment regimens; six had dissemination. Patients received initial bevacizumab-based therapy at a median age of 5.3 years (range, 112 years). Median treatment duration was 12 months (range, 124 months). 12 patients had an objective response; 2 had stable disease. Median time to maximum response was 9 weeks (range, 717 weeks). No patients progressed on therapy, although 13/14 progressed after stopping bevacizumab at a median of 5 months. Four patients were re-treated with bevacizumab and all again responded or stabilized. Alternative dosing strategies were effective, including bevacizumab monotherapy and prolonging the dosing interval to 3 weeks. High-grade bevacizumab-related toxicities consisted of grade 3 proteinuria (n=2), primary inflammatory arthritis (n=1), and somnolence (n=1). Toxicities resolved within 6 months of treatment cessation except one case of hypertension. Conclusions Bevacizumab-based therapy is successful at inducing rapid LGG response. Patients progressing off-therapy may be successfully re-treated with bevacizumab. Nearly all tumors progress once treatment is discontinued. Toxicities are not insignificant but usually reversible. Pediatr Blood Cancer 2013; 60: 776782. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:776 / 782
页数:7
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