Diagnosis of GH deficiency as a late effect of radiotherapy in survivors of childhood cancers
Journal of Clinical Endocrinology & Metabolism Aug 11, 2018
Sfeir JG, et al. - Researchers investigated how to choose a laboratory method for diagnosing GH deficiency (GHD) when it happens as a late effect of radiotherapy in childhood cancer survivors (CCSs). The diagnostic accuracy of various dynamic tests for GHD in CCSs vs non-CCSs seemed to follow the same patterns. Given the primarily hypothalamic dysfunction in CCSs, interpreting GHRH stimulation is a challenge. In this population, IGF-1 and IGF-binding protein 3 (IGFBP-3) performed poorly.
Methods
- Medline, Embase, Cochrane Central Register of Controlled Trials and Database of Systematic Reviews, and Scopus were searched for studies evaluating GHD.
- Studies using IGF-1 or IGFBP-3 measurements compared with GH dynamic testing were identified.
Results
- Fifteen studies (IGF-1 [8 studies] and IGFBP-3 [7 studies]) enrolling 477 patients were included.
- Wide variation in comparator tests was noted.
- Although strongly correlated, both IGF-1 and IGFBP-3 had suboptimal diagnostic accuracy, and simultaneous use of both tests in the same cohort did not improve the diagnostic accuracy.
- For appropriately identifying patients with GHD, dynamic tests remained the most accurate despite high variability in the testing protocols.
- Outcomes suggest the insulin tolerance test (ITT) to be the most accepted reference test when used alone or in combination with arginine; however, among practice groups, there were no standardized testing strategies.
- GHRH and arginine stimulation were almost similar to ITT regarding their performance; however, one study displayed 66% sensitivity and 88% specificity for GHRH with arginine stimulation compared with the ITT.
- They identified no sufficient data assessing the accuracy of serial GH testing (nocturnal or over 24 hours).
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