Hypothalamic-pituitary-adrenal (HPA) axis suppression after treatment with glucocorticoid therapy for childhood acute lymphoblastic leukaemia.
Abstract
BACKGROUND
Glucocorticoids play a major role in the treatment of acute lymphoblastic leukaemia (ALL). However, supraphysiological doses
may cause suppression of the hypothalamic-pituitary-adrenal (HPA) axis. HPA axis suppression resulting in reduced cortisol
response may cause an impaired stress response and an inadequate host defence against infections, which remains a cause of
morbidity and death. The exact occurrence and duration of HPA axis suppression after glucocorticoid therapy for childhood
ALL are unclear.
OBJECTIVES
To examine the occurrence and duration of HPA axis suppression after (each cycle of) glucocorticoid therapy for childhood
ALL.
SEARCH METHODS
We searched the Cochrane Central Register of Controlled Trials (in The Cochrane Library, issue 3, 2010), MEDLINE/PubMed (from
1945 to July 2010) and EMBASE/Ovid (from 1980 to July 2010). In addition, we searched reference lists of relevant articles,
conference proceedings and ongoing trial databases.
SELECTION CRITERIA
All study designs, except case reports and patient series with fewer than 10 patients, examining the effect of glucocorticoid
therapy for childhood ALL on the HPA axis function.
DATA COLLECTION AND ANALYSIS
Two review authors independently performed the study selection. One review author performed the data extraction and 'Risk
of bias' assessment, which was checked by another review author.
MAIN RESULTS
We identified seven studies (total number of participants = 189), including one randomised controlled trial (RCT), which assessed
the adrenal function. None of the studies assessed the HPA axis at the level of the hypothalamus, pituitary, or both. Due
to substantial differences between studies, results could not be pooled. All studies had some methodological limitations.
The included studies demonstrated that adrenal insufficiency occurs in nearly all patients in the first days after cessation
of glucocorticoid treatment for childhood ALL. The majority of patients recovered within a few weeks, but a small amount of
patients had ongoing adrenal insufficiency lasting up to 34 weeks. In the RCT, the occurrence and duration of adrenal insufficiency
did not differ between the prednisolone and dexamethasone arms. In one study included in the review it appeared that treatment
with fluconazole prolonged the duration of adrenal insufficiency.
AUTHORS' CONCLUSIONS
Based on the available evidence, we conclude that adrenal insufficiency commonly occurs in the first days after cessation
of glucocorticoid therapy for childhood ALL, but the exact duration is unclear. Since no data on the level of the hypothalamus
and the pituitary were available we cannot make any conclusions regarding those outcomes. Clinicians should consider prescribing
glucocorticoid replacement therapy during periods of serious stress in the first weeks after cessation of glucocorticoid therapy
for childhood ALL, to reduce the risk of life-threatening complications. However, more high-quality research is needed for
evidence-based guidelines for glucocorticoid replacement therapy.Special attention should be paid to patients receiving fluconazole
therapy, and perhaps similar antifungal drugs, as this may prolong the duration of adrenal insufficiency.
Links
Authors
Gordijn MS, Gemke RJ, van Dalen EC, Rotteveel J, Kaspers GJ
Institution
Department of Pediatrics, Division of Oncology/Hematology, VU University Medical Center, Amsterdam, Netherlands.ms.gordijn@vumc.nl.
Source
Cochrane database of systematic reviews (Online) 5: 2012 pg CD008727MeSH
Adrenal InsufficiencyAntineoplastic Agents, Hormonal
Child
Cohort Studies
Dexamethasone
Glucocorticoids
Humans
Hypothalamo-Hypophyseal System
Pituitary-Adrenal System
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Prednisolone
Randomized Controlled Trials as Topic
Pub Type(s)
Journal ArticleResearch Support, Non-U.S. Gov't
Review
Language
eng
PubMed ID
22592733
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