TY - JOUR
T1 - Mucormycosis in children with haematological malignancies is a salvageable disease
T2 - a report from the Israeli Study Group of Childhood Leukemia
AU - Elitzur, Sarah
AU - Arad-Cohen, Nira
AU - Barg, Assaf
AU - Litichever, Naomi
AU - Bielorai, Bella
AU - Elhasid, Ronit
AU - Fischer, Salvador
AU - Fruchtman, Yariv
AU - Gilad, Gil
AU - Kapelushnik, Joseph
AU - Kharit, Mira
AU - Konen, Osnat
AU - Laor, Ruth
AU - Levy, Itzhak
AU - Raviv, Dror
AU - Shachor-Meyouhas, Yael
AU - Shvartser-Beryozkin, Yulia
AU - Toren, Amos
AU - Yaniv, Isaac
AU - Nirel, Ronit
AU - Izraeli, Shai
AU - Barzilai-Birenboim, Shlomit
N1 - Publisher Copyright:
© 2019 British Society for Haematology and John Wiley & Sons Ltd
PY - 2020/4/1
Y1 - 2020/4/1
N2 - Mucormycosis has emerged as an increasingly important cause of morbidity and mortality in immunocompromised patients, but contemporary data in children are lacking. We conducted a nationwide multicentre study to investigate the characteristics of mucormycosis in children with haematological malignancies. The cohort included 39 children with mucormycosis: 25 of 1136 children (incidence 2·2%) with acute leukaemias prospectively enrolled in a centralized clinical registry in 2004–2017, and an additional 14 children with haematological malignancies identified by retrospective search of the databases of seven paediatric haematology centres. Ninety-two percent of mucormycosis cases occurred in patients with acute leukaemias. Mucormycosis was significantly associated with high-risk acute lymphoblastic leukaemia (OR 3·75; 95% CI 1·51–9·37; P = 0·004) and with increasing age (OR 3·58; 95% CI 1·24–9·77; P = 0·01). Fifteen patients (38%) died of mucormycosis. Rhinocerebral pattern was independently associated with improved 12-week survival (OR 9·43; 95% CI 1·47–60·66; P = 0·02) and relapsed underlying malignancy was associated with increased 12-week mortality (OR 6·42; 95% CI, 1·01–40·94; P = 0·05). In patients receiving frontline therapy for their malignancy (n = 24), one-year cumulative mucormycosis-related mortality was 21 ± 8% and five-year overall survival was 70 ± 8%. This largest paediatric population-based study of mucormycosis demonstrates that children receiving frontline therapy for their haematological malignancy are often salvageable.
AB - Mucormycosis has emerged as an increasingly important cause of morbidity and mortality in immunocompromised patients, but contemporary data in children are lacking. We conducted a nationwide multicentre study to investigate the characteristics of mucormycosis in children with haematological malignancies. The cohort included 39 children with mucormycosis: 25 of 1136 children (incidence 2·2%) with acute leukaemias prospectively enrolled in a centralized clinical registry in 2004–2017, and an additional 14 children with haematological malignancies identified by retrospective search of the databases of seven paediatric haematology centres. Ninety-two percent of mucormycosis cases occurred in patients with acute leukaemias. Mucormycosis was significantly associated with high-risk acute lymphoblastic leukaemia (OR 3·75; 95% CI 1·51–9·37; P = 0·004) and with increasing age (OR 3·58; 95% CI 1·24–9·77; P = 0·01). Fifteen patients (38%) died of mucormycosis. Rhinocerebral pattern was independently associated with improved 12-week survival (OR 9·43; 95% CI 1·47–60·66; P = 0·02) and relapsed underlying malignancy was associated with increased 12-week mortality (OR 6·42; 95% CI, 1·01–40·94; P = 0·05). In patients receiving frontline therapy for their malignancy (n = 24), one-year cumulative mucormycosis-related mortality was 21 ± 8% and five-year overall survival was 70 ± 8%. This largest paediatric population-based study of mucormycosis demonstrates that children receiving frontline therapy for their haematological malignancy are often salvageable.
KW - children
KW - fungal infections
KW - hematological malignancies
KW - leukemia
KW - mucormycosis
UR - http://www.scopus.com/inward/record.url?scp=85077859716&partnerID=8YFLogxK
U2 - 10.1111/bjh.16329
DO - 10.1111/bjh.16329
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C2 - 31885080
AN - SCOPUS:85077859716
SN - 0007-1048
VL - 189
SP - 339
EP - 350
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 2
ER -