TY - JOUR
T1 - Infections in pediatric acute promyelocytic leukemia
T2 - From the canadian infections in acute myeloid leukemia research group
AU - Cellot, Sonia
AU - Johnston, Donna
AU - Dix, David
AU - Ethier, Marie Chantal
AU - Gillmeister, Biljana
AU - Mitchell, David
AU - Yanofsky, Rochelle
AU - Lewis, Victor
AU - Portwine, Carol
AU - Price, Victoria
AU - Zelcer, Shayna
AU - Silva, Mariana
AU - Bowes, Lynette
AU - Michon, Bruno
AU - Stobart, Kent
AU - Brossard, Josee
AU - Beyene, Joseph
AU - Sung, Lillian
N1 - Funding Information:
This work was supported by the Canadian Cancer Society (Grant #019468) and the C17 Research Network. LS is supported by a New Investigator Award from the Canadian Institutes of Health Research.
PY - 2013/6/4
Y1 - 2013/6/4
N2 - Background: It is not known whether children with acute promyelocytic leukemia (APL) have an infection risk similar to non- APL acute myeloid leukemia. The objective was to describe infectious risk in children with newly diagnosed APL and to describe factors associated with these infections.Methods: We conducted a retrospective, population-based cohort study that included children ≤ 18 years of age with de novo APL treated at 15 Canadian centers. Thirty-three children with APL were included; 78.8% were treated with APL -specific protocols.Results: Bacterial sterile site infection occurred in 12 (36.4%) and fungal sterile site infection occurred in 2 (6.1%) children. Of the 127 chemotherapy courses, 101 (79.5%) were classified as intensive and among these, the proportion in which a sterile site microbiologically documented infection occurred was 14/101 (13.9%). There was one infection-related death.Conclusions: One third of children with APL experienced at least one sterile site bacterial infection throughout treatment and 14% of intensive chemotherapy courses were associated with a microbiologically documented sterile site infection. Infection rates in pediatric APL may be lower compared to non- APL acute myeloid leukemia although these children may still benefit from aggressive supportive care during intensive chemotherapy.
AB - Background: It is not known whether children with acute promyelocytic leukemia (APL) have an infection risk similar to non- APL acute myeloid leukemia. The objective was to describe infectious risk in children with newly diagnosed APL and to describe factors associated with these infections.Methods: We conducted a retrospective, population-based cohort study that included children ≤ 18 years of age with de novo APL treated at 15 Canadian centers. Thirty-three children with APL were included; 78.8% were treated with APL -specific protocols.Results: Bacterial sterile site infection occurred in 12 (36.4%) and fungal sterile site infection occurred in 2 (6.1%) children. Of the 127 chemotherapy courses, 101 (79.5%) were classified as intensive and among these, the proportion in which a sterile site microbiologically documented infection occurred was 14/101 (13.9%). There was one infection-related death.Conclusions: One third of children with APL experienced at least one sterile site bacterial infection throughout treatment and 14% of intensive chemotherapy courses were associated with a microbiologically documented sterile site infection. Infection rates in pediatric APL may be lower compared to non- APL acute myeloid leukemia although these children may still benefit from aggressive supportive care during intensive chemotherapy.
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U2 - 10.1186/1471-2407-13-276
DO - 10.1186/1471-2407-13-276
M3 - Article
C2 - 23735034
AN - SCOPUS:84878391882
SN - 1471-2407
VL - 13
JO - BMC Cancer
JF - BMC Cancer
M1 - 276
ER -