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Effects of Growth Hormone Replacement Therapy in Childhood-onset Craniopharyngioma: an Updated Systematic Review and Meta-analysis

Overview
Journal Pituitary
Specialty Endocrinology
Date 2024 Dec 26
PMID 39724512
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Abstract

Purpose: Craniopharyngiomas (CPs) often lead to growth hormone deficiency (GHD) in children. Growth hormone replacement therapy (GHRT) is essential for managing GHD but its impact on body mass index (BMI) and metabolic outcomes is controversial. Concerns exist that GHRT might contribute to tumor recurrence, with guidelines varying on when to start therapy post-surgery. This updated systematic review and meta-analysis explores the effects and timing of GHRT in children post-craniopharyngioma surgery.

Methods: We systematically searched PubMed, Embase, and Cochrane Library databases. Included studies compared the effects of GHRT in childhood-onset craniopharyngioma patients who received GHRT versus those who did not. Random-effects meta-analyses were used to pool relative risk (RR) or mean difference (MD) for each outcome. Heterogeneity was assessed using the I² statistic. This study is registered with PROSPERO (CRD42024498082).

Results: We included 11 studies in the meta-analysis. No differences in tumor progression/recurrence were found between the GHRT and no GHRT groups (RR 0.77, 95% CI 0.56-1.05, p = 0.10). The impact of timing of GHRT is less clear because of limited data and high heterogeneity. There were no differences in BMI between the GHRT and no GHRT (MD -0.94, 95% CI -1.88,0.00, p = 0.05). Two studies reported that GHRT might improve lipid profiles.

Conclusion: Our study suggests that GHRT does not increase the risk of tumor progression/recurrence in CP patients. GHRT can improve linear growth, but its effects on the BMI and lipid profiles remain inconclusive, requiring further studies.

References
1.
Boguszewski M, Cardoso-Demartini A, Boguszewski C, Chemaitilly W, Higham C, Johannsson G . Safety of growth hormone (GH) treatment in GH deficient children and adults treated for cancer and non-malignant intracranial tumors-a review of research and clinical practice. Pituitary. 2021; 24(5):810-827. PMC: 8416866. DOI: 10.1007/s11102-021-01173-0. View

2.
Muller H, Merchant T, Warmuth-Metz M, Martinez-Barbera J, Puget S . Craniopharyngioma. Nat Rev Dis Primers. 2019; 5(1):75. DOI: 10.1038/s41572-019-0125-9. View

3.
Zhou Z, Zhang S, Hu F . Endocrine Disorder in Patients With Craniopharyngioma. Front Neurol. 2021; 12:737743. PMC: 8675636. DOI: 10.3389/fneur.2021.737743. View

4.
Wijnen M, Olsson D, van den Heuvel-Eibrink M, Hammarstrand C, Janssen J, van der Lely A . Excess morbidity and mortality in patients with craniopharyngioma: a hospital-based retrospective cohort study. Eur J Endocrinol. 2017; 178(1):93-102. DOI: 10.1530/EJE-17-0707. View

5.
Geffner M, Lundberg M, Koltowska-Haggstrom M, Abs R, Verhelst J, Erfurth E . Changes in height, weight, and body mass index in children with craniopharyngioma after three years of growth hormone therapy: analysis of KIGS (Pfizer International Growth Database). J Clin Endocrinol Metab. 2004; 89(11):5435-40. DOI: 10.1210/jc.2004-0667. View