TY - JOUR
T1 - Prevalence and risk factors of radiation-induced growth hormone deficiency in childhood cancer survivors
T2 - A systematic review
AU - Mulder, Renée L.
AU - Kremer, Leontien C.M.
AU - Santen, Hanneke M.van
AU - Ket, Jan Lucas
AU - Trotsenburg, A. S.Paul van
AU - Koning, Caro C.E.
AU - Meeteren, Antoinette Y.N.Schouten van
AU - Caron, Huib N.
AU - Neggers, Sebastian J.C.M.M.
AU - Dalen, Elvira C.van
N1 - Funding Information:
The authors like to thank Edith Leclercq, for composing the search strategy and running it in the different databases, Jos Noorman, for helping to obtain the full text articles and Cécile Ronckers, for critically appraising the manuscript. This study was supported by the Foundation of Paediatric Cancer Research (SKK), Amsterdam, the Netherlands, and Stichting Kinderen Kankervrij (KiKa), the Netherlands. The study sponsors had no involvement in the design and execution of the study, in writing the manuscript and in the decision to submit it for publication.
PY - 2009/11
Y1 - 2009/11
N2 - Background: Growth hormone deficiency (GHD) is usually the first and most frequent endocrine problem occurring after cranial radiotherapy (CRT). The aim of this systematic review was to evaluate the existing evidence of the prevalence and risk factors of radiation-induced GHD in childhood cancer survivors. Methods: MEDLINE, EMBASE and CENTRAL were searched for studies reporting on radiation-induced GHD in childhood cancer survivors. Information about study characteristics, prevalence and risk factors was abstracted and the quality of each study was assessed. A meta-regression analysis was performed. Results: The prevalence of radiation-induced GHD was estimated in 33 studies. Most studies had methodological limitations. The prevalence varied considerably between 0% and 90.9%. Selecting only the studies with adequate peak GH cut-off limits (<5 μg/L) resulted in 3 studies. In these studies the prevalence ranged from 29.0% to 39.1%, with a pooled prevalence of 35.6%. Higher CRT dose and longer follow-up time have been suggested to be the main risk factors of GHD by studies included in this review. The meta-regression analysis showed that the wide variation in the prevalence of GHD could be explained by differences in maximal CRT dose. Conclusions: GHD is a frequent consequence after CRT in childhood cancer survivors. The prevalence of radiation-induced GHD ranged from 29.0% to 39.1% when selecting only studies with adequate peak GH cut-off limits. Higher CRT dose and longer follow-up time are the main risk factors. More well-designed studies are needed to accurately estimate the prevalence of GHD and to define the exact CRT threshold dose.
AB - Background: Growth hormone deficiency (GHD) is usually the first and most frequent endocrine problem occurring after cranial radiotherapy (CRT). The aim of this systematic review was to evaluate the existing evidence of the prevalence and risk factors of radiation-induced GHD in childhood cancer survivors. Methods: MEDLINE, EMBASE and CENTRAL were searched for studies reporting on radiation-induced GHD in childhood cancer survivors. Information about study characteristics, prevalence and risk factors was abstracted and the quality of each study was assessed. A meta-regression analysis was performed. Results: The prevalence of radiation-induced GHD was estimated in 33 studies. Most studies had methodological limitations. The prevalence varied considerably between 0% and 90.9%. Selecting only the studies with adequate peak GH cut-off limits (<5 μg/L) resulted in 3 studies. In these studies the prevalence ranged from 29.0% to 39.1%, with a pooled prevalence of 35.6%. Higher CRT dose and longer follow-up time have been suggested to be the main risk factors of GHD by studies included in this review. The meta-regression analysis showed that the wide variation in the prevalence of GHD could be explained by differences in maximal CRT dose. Conclusions: GHD is a frequent consequence after CRT in childhood cancer survivors. The prevalence of radiation-induced GHD ranged from 29.0% to 39.1% when selecting only studies with adequate peak GH cut-off limits. Higher CRT dose and longer follow-up time are the main risk factors. More well-designed studies are needed to accurately estimate the prevalence of GHD and to define the exact CRT threshold dose.
KW - Childhood cancer survivors
KW - Cranial radiotherapy
KW - Growth hormone deficiency
KW - Systematic review
UR - http://www.scopus.com/inward/record.url?scp=70350405324&partnerID=8YFLogxK
U2 - 10.1016/j.ctrv.2009.06.004
DO - 10.1016/j.ctrv.2009.06.004
M3 - Review article
C2 - 19640651
AN - SCOPUS:70350405324
SN - 0305-7372
VL - 35
SP - 616
EP - 632
JO - Cancer Treatment Reviews
JF - Cancer Treatment Reviews
IS - 7
ER -