Context: 50% of pediatric low-grade gliomas affect the optic pathway, hypothalamus and suprasellar
areas (OP/HSGs) resulting in significant long-term neuroendocrinopathy.
Objective: To dissect tumor- from treatment-related risk factors for OP/HSG-associated
neuroendocrinopathy.
Design: Retrospective case notes analysis of 166 children with newly-diagnosed OP/HSGs at our
quaternary center between 1980 –2010 by multivariate Cox, linear and logistic regression.
Results: Patients were of median (range) age 4.9 (0.2–15.4) years at diagnosis and followed up for
8.3 (0.04 –26.8) years. Despite high 20-year overall survival (81.0%), progression-free and endocrine
event-free (EEFS) survival were 47.2% and 20.8% respectively. EEFS declined up to 15 years postdiagnosis,
with hypothalamic involvement (p0.001) being implicated more than radiotherapy
(p0.008) in earlier endocrinopathy; the reverse being true of its density (radiotherapy p0.001;
hypothalamic involvement p0.006). GH deficiency (GHD) was commonest (40.3%), followed by
central precocious puberty (CPP, 26.0%), gonadotropin (GnD, 20.4%), TSH (13.3%), and ACTH
(13.3%) deficiencies. GHD increased with later treatment eras (p0.01), but replacement did not
increase progression. CPP was associated with future GnD (p0.05). Posterior pituitary dysfunction
(PPD, 7.2%) occurred in 57.9% after only biopsies or shunt procedures, and was associated with 6/13
deaths. 50.2% became obese. Tumor extent, surgery and increased endocrinopathy, rather than
radiotherapy, predicted visuo-cognitive morbidity.
Conclusions: This first longitudinal OP/HSG-specific study demonstrates that hypothalamo-pituitary
dysfunction evolves hierarchically over decades. Tumor location predicts its speed of onset and
radiotherapy its density. GnD can evolve from previous CPP, whilst life-threatening PPD can occur
after any surgery. Our data suggest that recent radiation-avoiding chemotherapeutic strategies
have increased GHD without improving survival
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