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The Journal of Clinical Endocrinology & Metabolism Vol. 86, No. 7 2993-2996
Copyright © 2001 by The Endocrine Society


Endocrine Care

Evaluation of the Hypothalamic-Pituitary-Adrenal Axis in Children with Leukemia before and after 6 Weeks of High-Dose Glucocorticoid Therapy

Hilton Kuperman, Durval Damiani, George P. Chrousos, Vaê Dichtchekenian, Thais Della Manna, Vicente Odone Filho and Nuvarte Setian

Departments of Pediatric Endocrinology (H.K., D.D., V.D., T.D.M., N.S.) and Oncology (V.O.F.) of the Children’s Hospital, São Paulo University School of Medicine-Brazil; and Pediatric and Reproductive Endocrinology Branch, National Institute of Child Health and Human Development (G.P.C.), National Institutes of Health, Bethesda, Maryland

Address all correspondence and requests for reprints to: Hilton Kuperman, M.D., University of São Paulo, Department of Pediatric Endocrinology, Children’s Hospital, Faculty of Medicine, Rua Conselheiro Brotero 1182, apt. 182, São Paulo, Brazil 01232-010. E-mail: hkuperman{at}terra com.br.

Abstract

Among the adverse effects arising from chronic high-dose glucocorticoid treatment, adrenal insufficiency secondary to suppression of the hypothalamic-pituitary-adrenal (HPA) axis is a cause for concern. Glucocorticoid-induced adrenal suppression is related to the duration of therapy, type of steroid used and dosage, and schedule of glucocorticoid administration. To evaluate the suppression and recovery time of the HPA axis in children with acute leukemia, we performed the ovine CRH (oCRH) stimulation test in 15 patients, who were given high doses of dexamethasone as part of their induction chemotherapy for 42 days. The oCRH tests were performed before, and 7 and 14 days after, discontinuation of the glucocorticoid. The ACTH levels were not significantly different among the 3 tests. The cortisol levels, however, were significantly (albeit mildly) lower, both basally and after oCRH, 1 and 2 weeks post treatment than before therapy. Six patients had cortisol values that remained suppressed 2 weeks after discontinuation of therapy. One of these patients had manifestations of mild adrenal insufficiency, 6–8 days after discontinuation of therapy, but required no glucocorticoid coverage. We conclude that up to 2 weeks after discontinuation of 6 weeks of high-dose dexamethasone administration, the HPA axis of patients with acute leukemia is mildly suppressed but infrequently associated with clinical manifestations of adrenal insufficiency. This may indicate that major stress, when concurrent with glucocorticoid treatment, may prevent clinically significant adrenal suppression.




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