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Publication Date:
December 2010
ISSN:
2191-0251
DOI:
10.1515/jpem.2010.150

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Editor-in-Chief: Zadik, Zvi

Editorial Board Member: Cassorla, Fernando / Cutfield, Wayne / de Muinck Keizer-Schrama, Sabine M.P.F. / Fideleff, Hugo L. / LaFranch, Stephen H. / Lanes M. D., Roberto / Levitsky, Lynne / Lippe, Barbara / Pfäffle, Roland / Root, Allen W. / Rosenfeld, Ron G. / Werther, George / Kiess, Wieland

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Growth Hormone Therapy and the Risk of Tumor Recurrence after Brain Tumor Treatment in Children

Tilman R. Rohrer1 / Thorsten Langer2 / Gerhard G. Grabenbauer3 / Michael Buchfelder4 / Matthias Glowatzki5 / Helmuth G. Dörr2

1Department of Pediatrics and Adolescent Medicine; Saarland University Hospital, Homburg/Saar, Germany

2Hospital for Children and Adolescents, University of Erlangen-Nuremberg, Erlangen, Germany

3Department of Radiotherapy, University of Erlangen-Nuremberg, Erlangen, Germany

4Department of Neurosurgery, University of Erlangen-Nuremberg, Erlangen, Germany

5SPSS GmbH Software, Munich, Germany

c1Corresponding author: Professor Dr. Helmuth Dörr,

Citation Information: Journal of Pediatric Endocrinology and Metabolism. Volume 23, Issue 9, Pages 935–942, ISSN (Online) 2191-0251, ISSN (Print) 0334-018X, DOI: 10.1515/jpem.2010.150, December 2010

Publication History:
Published Online:
2010-12-22

ABSTRACT

To assess the effect of human growth hormone (hGH) therapy and other factors on tumor recurrence after treatment of pediatric brain tumors (BTs), we retrospectively analyzed data from 108 craniopharyngioma, medulloblastoma, and ependymoma patients. Risk factors were identified using multifactorial univariate regression analysis. Recurrences occurred in 41 and second malignant neoplasms in 4 patients. There were significant correlations for completeness of tumor removal and recurrence-free survival (RFS). 13/44 hGH-treated and 28/59 non-hGH-treated children relapsed. This difference was found only for medulloblastomas and accounted for by higher rates of incomplete tumor removal in non-hGH patients. Craniopharyngioma recurrence correlated only with RFS. Malignant BT recurrence correlated with completeness of tumor removal, chemotherapy, and RFS. 4 children developed SMNs, 3/4 after hGH therapy. Our regression model yielded accurate within-sample prediction of recurrence for 90% of the study population. We conclude that hGH therapy after treatment of pediatric BTs does not increase tumor recurrence risk.

KEY WORDS: GH replacement therapy; pediatric brain tumor recurrence; craniopharyngioma; medulloblastoma; ependymoma; relapse risk; childhood brain tumor

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