TY - JOUR
T1 - Assessment of Puberty and Hypothalamic–Pituitary–Gonadal Axis Function After Childhood Brain Tumor Treatment
AU - Rosimont, Manon
AU - Kariyawasam, Dulanjalee
AU - Samara-Boustani, Dinane
AU - Giani, Elisa
AU - Beltrand, Jacques
AU - Bolle, Stephanie
AU - Fresneau, Brice
AU - Puget, Stephanie
AU - Sainte-Rose, Christian
AU - Alapetite, Claire
AU - Pinto, Graziella
AU - Touraine, Philippe
AU - Piketty, Marie Liesse
AU - Brabant, Séverine
AU - Abbou, Samuel
AU - Aerts, Isabelle
AU - Beccaria, Kevin
AU - Bourgeois, Marie
AU - Roujeau, Thomas
AU - Blauwblomme, Thomas
AU - Rocco, Federico Di
AU - Thalassinos, Caroline
AU - Rigaud, Charlotte
AU - James, Syril
AU - Busiah, Kanetee
AU - Simon, Albane
AU - Bourdeaut, Franck
AU - Lemelle, Lauriane
AU - Guerrini-Rousseau, Léa
AU - Orbach, Daniel
AU - Doz, François
AU - Dufour, Christelle
AU - Grill, Jacques
AU - Polak, Michel
AU - Briceño, Laura González
N1 - Publisher Copyright:
© The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved.
PY - 2023/9/1
Y1 - 2023/9/1
N2 - Context: Endocrine complications are common in pediatric brain tumor patients. Objective: To describe hypothalamic–pituitary–gonadal axis (HPGA) function in patients treated in childhood for a primary brain tumor more than 5 years earlier, in order to identify risk factors for HPGA impairment. Methods: We retrospectively included 204 patients diagnosed with a primary brain tumor before 18 years of age and monitored at the pediatric endocrinology unit of the Necker Enfants-Malades University Hospital (Paris, France) between January 2010 and December 2015. Patients with pituitary adenoma or untreated glioma were excluded. Results: Among patients with suprasellar glioma not treated by radiotherapy, the prevalence of advanced puberty was 65% overall and 70% when the diagnosis occurred before 5 years of age. Medulloblastoma chemotherapy caused gonadal toxicity in 70% of all patients and in 87.5% of those younger than 5 years at diagnosis. In the group with craniopharyngioma, 70% of patients had hypogonadotropic hypogonadism, which was consistently accompanied by growth hormone deficiency. Conclusion: Tumor type, location, and treatment were the risk main factors for HPGA impairment. Awareness that onset can be delayed is essential to guide information of parents and patients, patient monitoring, and timely hormone replacement therapy.
AB - Context: Endocrine complications are common in pediatric brain tumor patients. Objective: To describe hypothalamic–pituitary–gonadal axis (HPGA) function in patients treated in childhood for a primary brain tumor more than 5 years earlier, in order to identify risk factors for HPGA impairment. Methods: We retrospectively included 204 patients diagnosed with a primary brain tumor before 18 years of age and monitored at the pediatric endocrinology unit of the Necker Enfants-Malades University Hospital (Paris, France) between January 2010 and December 2015. Patients with pituitary adenoma or untreated glioma were excluded. Results: Among patients with suprasellar glioma not treated by radiotherapy, the prevalence of advanced puberty was 65% overall and 70% when the diagnosis occurred before 5 years of age. Medulloblastoma chemotherapy caused gonadal toxicity in 70% of all patients and in 87.5% of those younger than 5 years at diagnosis. In the group with craniopharyngioma, 70% of patients had hypogonadotropic hypogonadism, which was consistently accompanied by growth hormone deficiency. Conclusion: Tumor type, location, and treatment were the risk main factors for HPGA impairment. Awareness that onset can be delayed is essential to guide information of parents and patients, patient monitoring, and timely hormone replacement therapy.
KW - brain tumor
KW - childhood cancer
KW - endocrine disorders
UR - http://www.scopus.com/inward/record.url?scp=85168315855&partnerID=8YFLogxK
U2 - 10.1210/clinem/dgad097
DO - 10.1210/clinem/dgad097
M3 - Article
C2 - 36810692
AN - SCOPUS:85168315855
SN - 0021-972X
VL - 108
SP - E823-E831
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 9
ER -