Dosimetry and growth hormone deficiency following cranial irradiation of childhood brain tumors

Citation
M. Schmiegelow et al., Dosimetry and growth hormone deficiency following cranial irradiation of childhood brain tumors, MED PED ONC, 33(6), 1999, pp. 564-571
Citations number
46
Categorie Soggetti
Pediatrics
Journal title
MEDICAL AND PEDIATRIC ONCOLOGY
ISSN journal
00981532 → ACNP
Volume
33
Issue
6
Year of publication
1999
Pages
564 - 571
Database
ISI
SICI code
0098-1532(199912)33:6<564:DAGHDF>2.0.ZU;2-P
Abstract
Background, Dosimetry of the hypothalamus-pituitary (HP) region could allow prediction of the risk of growth hormone deficiency (CHD) following crania l irradiation. Procedure. Nineteen children (15 boys) with a median age of 6.3 years (range 1.7-16.5) at the time of irradiation of a brain tumor not involving the HP axis were followed for 1.2-6.3 years (median 3.4) from rad iotherapy (RT). The dose to a standardized anatomical model including the H P region was calculated from dose-volume histograms of 10% to 100% in steps of 10% of the HP model based on data from a computer-based treatment plann ing system, If GHD was suspected from insulin-like growth factor-I, serum i nsulin-like growth factor binding protein-3, and/or height velocity measure ments, an arginine stimulation test was performed. GHD was defined by a pea k GH <15mU/liter. Results. Ten patients developed GHD 10-26 months from irr adiation. Cox regression analysis identified the 90% dose-volume of the HP box as the strongest predictor of development of GHD (P = 0.03). The median dose to the 90% dose-volume of the HP region was 37.5 Gy (range 2.3-55.3). The cumulated risk of GHD 2.5 years after radiotherapy for children receiv ing more than and less than 37.5 Gy to the HP region was 87% and 33%, respe ctively (P = 0.036). Conclusions. Dosimetry of a defined HP volume provides the opportunity to 1) calculate the exact dose delivered to this region; 2 ) predict the risk of GHD and, 3) in the future revise the treatment planni ng and thus reduce the risk of endocrine adverse effects. Med. Pediatr. Onc ol. 33:564-571, 1999. (C) 1999 Wiley-Liss, Inc.