Bevacizumab for symptomatic radiation‐induced tumor enlargement in pediatric low grade gliomas. Issue 2 (8th November 2014)
- Record Type:
- Journal Article
- Title:
- Bevacizumab for symptomatic radiation‐induced tumor enlargement in pediatric low grade gliomas. Issue 2 (8th November 2014)
- Main Title:
- Bevacizumab for symptomatic radiation‐induced tumor enlargement in pediatric low grade gliomas
- Authors:
- Foster, Kimberly A.
Ares, William J.
Pollack, Ian F.
Jakacki, Regina I. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pbc25277-sec-0001" sec-type="section"> <title>Background</title> <p>Radiation therapy (RT)‐induced effects in children treated for low grade glioma (LGG) can result in worsening of neurologic symptoms and clinical and radiographic deterioration. Treatment for radiation‐induced tumor enlargement is based on symptom control and usually involves steroids.</p> </sec> <sec id="pbc25277-sec-0002" sec-type="section"> <title>Procedure</title> <p>We conducted a retrospective review of children with LGG treated with RT who developed symptomatic radiation‐induced tumor enlargement and were managed with bevacizumab. Charts were abstracted for onset and duration of RT changes, toxicity and doses of dexamethasone and bevacizumab. Tumor volumes prior to RT, at maximal size following RT, after bevacizumab administration, and at follow‐up were evaluated.</p> </sec> <sec id="pbc25277-sec-0003" sec-type="section"> <title>Results</title> <p>Five children were treated with bevacizumab for symptomatic radiation‐induced tumor enlargement following RT for LGG at a median of 4.2 months (range, 1–11 months) after completion of RT. The median increase in volume of tumor was 195.4% (range, 115.5–309%) compared to the pre‐RT volume. Bevacizumab 5–10 mg/kg was administered IV q 2–4 weeks as primary treatment (n = 1) or to assist in weaning patients off steroids (n = 4). All children on high dose steroids<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pbc25277-sec-0001" sec-type="section"> <title>Background</title> <p>Radiation therapy (RT)‐induced effects in children treated for low grade glioma (LGG) can result in worsening of neurologic symptoms and clinical and radiographic deterioration. Treatment for radiation‐induced tumor enlargement is based on symptom control and usually involves steroids.</p> </sec> <sec id="pbc25277-sec-0002" sec-type="section"> <title>Procedure</title> <p>We conducted a retrospective review of children with LGG treated with RT who developed symptomatic radiation‐induced tumor enlargement and were managed with bevacizumab. Charts were abstracted for onset and duration of RT changes, toxicity and doses of dexamethasone and bevacizumab. Tumor volumes prior to RT, at maximal size following RT, after bevacizumab administration, and at follow‐up were evaluated.</p> </sec> <sec id="pbc25277-sec-0003" sec-type="section"> <title>Results</title> <p>Five children were treated with bevacizumab for symptomatic radiation‐induced tumor enlargement following RT for LGG at a median of 4.2 months (range, 1–11 months) after completion of RT. The median increase in volume of tumor was 195.4% (range, 115.5–309%) compared to the pre‐RT volume. Bevacizumab 5–10 mg/kg was administered IV q 2–4 weeks as primary treatment (n = 1) or to assist in weaning patients off steroids (n = 4). All children on high dose steroids (n = 4) were weaned off or to physiologic doses of hydrocortisone. Two children developed avascular necrosis after prolonged steroid use and while on bevacizumab. Radiographically, all children showed significant improvement and are now a median of 31 months (range, 18–50 months) from the completion of radiation without requiring additional tumor‐related therapy.</p> </sec> <sec id="pbc25277-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Bevacizumab can play an important role in children with symptomatic radiation changes following LGG treatment, allowing patients to avoid or minimize the toxicity of long‐term steroid use. Pediatr Blood Cancer 2015;62:240–245. © 2014 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Pediatric blood & cancer. Volume 62:Issue 2(2015:Feb.)
- Journal:
- Pediatric blood & cancer
- Issue:
- Volume 62:Issue 2(2015:Feb.)
- Issue Display:
- Volume 62, Issue 2 (2015)
- Year:
- 2015
- Volume:
- 62
- Issue:
- 2
- Issue Sort Value:
- 2015-0062-0002-0000
- Page Start:
- 240
- Page End:
- 245
- Publication Date:
- 2014-11-08
- Subjects:
- Tumors in children -- Periodicals
Blood -- Diseases -- Periodicals
Cancer in children -- Periodicals
618.92 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1545-5017 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pbc.25277 ↗
- Languages:
- English
- ISSNs:
- 1545-5009
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6417.533500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3690.xml