Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/3465
Title: Invasive fungal disease in children with acute myeloid leukaemia: An Australian multicentre 10-year review
Authors: Blyth, C. C.
Clark, J. E. 
Haeusler, G. M.
Yeoh, D. K.
Moore, Andrew 
Kotecha, R. S.
Bartlett, A. W.
Ryan, A. L.
Cann, M. P.
McMullan, B. J.
Thursky, K.
Slavin, M.
Issue Date: 2021
Source: 68, (11), 2021
Journal: Pediatric Blood and Cancer
Abstract: Background: Invasive fungal disease (IFD) is a common and important complication in children with acute myeloid leukaemia (AML). We describe the epidemiology of IFD in a large multicentre cohort of children with AML. Methods: As part of the retrospective multicentre cohort TERIFIC (The Epidemiology and Risk factors for Invasive Fungal Infections in immunocompromised Children) study, proven/probable/possible IFD episodes occurring in children with primary or relapsed/refractory AML from 2003 to 2014 were analysed. Crude IFD prevalence, clinical characteristics, microbiology and treatment were assessed. Kaplan–Meier survival analysis was used to estimate 6-month survival. Results: There were 66 IFD episodes diagnosed in 63 children with AML. The majority (75.8%) of episodes occurred in the context of primary AML therapy. During primary AML therapy, the overall prevalence was 20.7% (95% CI 15.7%–26.5%) for proven/probable/possible IFD and 10.3% (95% CI 6.7%–15.0%) for proven/probable IFD. Of primary AML patients, 8.2% had IFD diagnosed during the first cycle of chemotherapy. Amongst pathogens implicated in proven/probable IFD episodes, 74.4% were moulds, over a third (37.9%) of which were non-Aspergillus spp. Antifungal prophylaxis preceded 89.4% of IFD episodes, most commonly using fluconazole (50% of IFD episodes). All-cause mortality at 6 months from IFD diagnosis was 16.7% with IFD-related mortality of 7.6% (all in cases of proven IFD). Conclusions: IFD is a common and serious complication during paediatric AML therapy. Mould infections, including non-Aspergillus spp. predominated in this cohort. A systematic approach to the identification of patients at risk, and a targeted prevention strategy for IFD is needed.L20133726562021-08-11
DOI: 10.1002/pbc.29275
Resources: https://www.embase.com/search/results?subaction=viewrecord&id=L2013372656&from=exporthttp://dx.doi.org/10.1002/pbc.29275 |
Keywords: hematopoietic stem cell transplantation;human;invasive aspergillosis;invasive candidiasis;Lomentospora prolificans;major clinical study;male;matched sibling donor;matched unrelated donor;monotherapy;neutropenia;nonhuman;pediatrics;Pichia kudriavzevii;prevalence;prophylaxis;retrospective study;treatment outcome;systemic mycosis;amphotericin B lipid complexantifungal agent;caspofungin;fluconazole;itraconazole;posaconazole;steroid;terbinafine;voriconazole;acute myeloid leukemia;adolescent;all cause mortality;article;Aspergillus;Australia;cancer chemotherapy;Candida albicans;candidemia;child;childhood mortality;cohort analysis;combination drug therapy;controlled study;female;graft versus host reaction
Type: Article
Appears in Sites:Children's Health Queensland Publications
Queensland Health Publications

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