Abstract
We report an increased incidence of infectious deaths during maintenance treatment of the ninth protocol for acute lymphoblastic leukaemia of the Dutch Childhood Oncology Group (DCOG-ALL-9). The main difference in maintenance treatment between DCCG-ALL-9 and the DCOG-ALL-7 and DCOG-ALL-8 protocols is the interruption of methotrexate and 6-mercaptopurine by vincristine (2 mg/m(2) weekly) and dexamethasone (6 mg/m(2) daily) for 14 days every 7 weeks in the DCOG-ALL-9 protocol. The 1107 children treated with the DCOG-ALL-7, DCOG-ALL-8 or DCOG-ALL-9 protocol were included and screened for infectious death during maintenance treatment (July 1988-July 2002). Seven of the 510 children died of severe infections during the maintenance phase of DCOG-ALL-9, compared to none of the 597 patients during the DCOG-ALL-7 and DCOG-ALL-8 protocols (1.37% versus 0.0%; p = 0.013). Results from the current study suggest that repeated, prolonged exposure to dexamethasone results in an increase of lethal infections from 0% to 1.37%. In the dosing-schedule used, the advantage of dexamethasone may not outweigh the higher risk of infectious death. (c) 2007 Elsevier Ltd. All rights reserved.
Original language | English |
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Pages (from-to) | 2532-2536 |
Number of pages | 5 |
Journal | European Journal of Cancer |
Volume | 43 |
Issue number | 17 |
DOIs | |
Publication status | Published - Nov-2007 |
Keywords
- acute lymphoblastic leukaemia
- all child
- dexamethasone
- glucocorticoids
- corticosteroids
- infection
- CORTICOTROPIN-RELEASING HORMONE
- ENDOTHELIAL-CELLS
- GLUCOCORTICOID THERAPY
- INTENSIVE TREATMENT
- MENINGEAL LEUKEMIA
- ADRENAL-FUNCTION
- CHILDREN
- PREDNISOLONE
- INDUCTION
- RAT