关于原发性非垂体脑肿瘤成人放疗诱发垂体功能减退症发生率的系统性回顾和荟萃分析。

IF 3 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Darran Mc Donald, Maria Tomkins, Liam O'Connell, David Fitzpatrick, Clare Faul, Michael W O'Reilly, Kathleen Bennett, Mark Sherlock
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Systematic Review and Meta-Analysis on the Prevalence of Radiotherapy-Induced Hypopituitarism in Adults With Primary Non-Pituitary Brain Tumours.

Context: It is well recognised there is a high prevalence of pituitary dysfunction in childhood brain tumours survivors who are treated with radiotherapy. In contrast, the potential for survivors of brain tumours arising in adulthood to develop radiotherapy-induced hypopituitarism may be underestimated. The aim of this systematic review and meta-analysis is to determine the pooled prevalence of radiotherapy-induced hypopituitarism in survivors of primary non-pituitary brain tumours arising in adulthood.

Design: A systematic literature search of five databases was performed. Two reviewers independently screened potential articles and then extracted data from accepted studies. A random effects meta-analysis was performed to assess the pooled prevalence of radiotherapy-induced hypopituitarism for each hormone axis. Forest plots were created to graphically represent these estimates with 95% confidence intervals (CI). Between study heterogeneity was quantified using the I2 statistic.

Results: Fourteen studies comprising a total of 580 participants were included in the review. The pooled prevalence of hypopituitarism was 48% (95% CI 36.7-59.4; I2 = 81%) with significant heterogeneity between study results. The pooled prevalence of growth hormone (GH) deficiency was 35.2% (95% CI 24.2-47.0; I2 = 81.4%), gonadotropin deficiency 20.9% (95% CI 14.4-28.1, I2 = 63.1%), adrenocorticotrophic hormone (ACTH) deficiency 16.0% (95% CI 11.4-21.1; I2 = 42.6%) and thyroid stimulating hormone (TSH) deficiency 18.2% (95% CI 12.3-24.8; I2 = 63.5%). Heterogeneity among study results was further evaluated through a meta-regression.

Conclusion: Radiotherapy-induced hypopituitarism is common, affecting almost half of survivors with a primary non-pituitary brain tumour arising in adulthood. Protocolised endocrine surveillance is essential in this cohort to identify and treat pituitary hormone deficits in a timely manner. These patients report decreased quality of life which may be due, in part, to undiagnosed pituitary dysfunction.

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来源期刊
Clinical Endocrinology
Clinical Endocrinology 医学-内分泌学与代谢
CiteScore
6.40
自引率
3.10%
发文量
192
审稿时长
1 months
期刊介绍: Clinical Endocrinology publishes papers and reviews which focus on the clinical aspects of endocrinology, including the clinical application of molecular endocrinology. It does not publish papers relating directly to diabetes care and clinical management. It features reviews, original papers, commentaries, correspondence and Clinical Questions. Clinical Endocrinology is essential reading not only for those engaged in endocrinological research but also for those involved primarily in clinical practice.
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