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Clinical impact of hypothalamic-pituitary disorders after conformal radiation therapy for pediatric low-grade glioma or ependymoma.
van Iersel, Laura; van Santen, Hanneke M; Potter, Brian; Li, Zhenghong; Conklin, Heather M; Zhang, Hui; Chemaitilly, Wassim; Merchant, Thomas E.
Afiliación
  • van Iersel L; Division of Endocrinology, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • van Santen HM; Department of Pediatric Endocrinology, Wilhelmina Children's Hospital, Utrecht, the Netherlands.
  • Potter B; Department of Pediatric Endocrinology, Wilhelmina Children's Hospital, Utrecht, the Netherlands.
  • Li Z; Department of Psychology, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Conklin HM; Department of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Zhang H; Department of Psychology, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Chemaitilly W; Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Merchant TE; Division of Endocrinology, St. Jude Children's Research Hospital, Memphis, Tennessee.
Pediatr Blood Cancer ; 67(12): e28723, 2020 12.
Article en En | MEDLINE | ID: mdl-33037871
ABSTRACT

BACKGROUND:

To determine the impact of hypothalamic-pituitary (HP) disorders on health outcomes in children and adolescents who received conformal radiation therapy (RT) for central nervous system tumors. PROCEDURE Cohort study including 355 patients (age ≤25 years at diagnosis) treated with high-dose (50.4-59.4 Gy) RT using photons for low-grade glioma or ependymoma. Patients (median age, 6.4 years at RT) received systematic endocrine follow-up (median duration, 10.1 years; range, 0.1-19.6). Associations between HP disorders and adverse health outcomes were determined by multivariable analysis.

RESULTS:

Prevalence was 37.2% for growth hormone deficiency (GHD), 17.7% for gonadotropin deficiency (LH/FSHD), 14.9% for thyroid-stimulating hormone deficiency (TSHD), 10.3% for adrenocorticotropic hormone deficiency (ACTHD), and 12.6% for central precocious puberty (CPP). Hypothalamus mean dose ≥ 36 Gy was associated with higher odds of any deficiency. GHD was associated with short stature (OR 2.77; 95% CI 1.34-5.70), low bone mineral density (OR 3.47; 95% CI 1.16-10.40), and TSHD with dyslipidemia (OR 5.54; 95% CI 1.66-18.52). Patients with ACTHD and CPP had lower intelligence quotient scores, and memory scores were impaired in patients with GHD (P = 0.02). Treatment of GHD was not associated with increased risk for tumor recurrence, secondary tumors, or mortality.

CONCLUSIONS:

HP disorders occur frequently in patients receiving high-dose RT and are related to physical and neurocognitive well-being. Future studies are needed to assess whether further optimization of endocrine management yields better health outcomes.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades de la Hipófisis / Hormona de Crecimiento Humana / Radioterapia Conformacional / Ependimoma / Glioma / Trastornos del Crecimiento / Enfermedades Hipotalámicas Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades de la Hipófisis / Hormona de Crecimiento Humana / Radioterapia Conformacional / Ependimoma / Glioma / Trastornos del Crecimiento / Enfermedades Hipotalámicas Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Año: 2020 Tipo del documento: Article