Epidemiology and outcome of invasive fungal disease in children after hematopoietic cell transplantation or treated for malignancy: Impact of national programme of antifungal prophylaxis

被引:11
|
作者
Czyzewski, Krzysztof [1 ]
Galazka, Przemyslaw [2 ]
Fraczkiewicz, Jowita [3 ]
Salamonowicz, Malgorzata [3 ]
Szmydki-Baran, Anna [4 ]
Zajac-Spychala, Olga [5 ]
Gryniewicz-Kwiatkowska, Olga [6 ]
Zalas-Wiecek, Patrycja [7 ]
Chelmecka-Wiktorczyk, Liliana [8 ]
Irga-Jaworska, Ninela [9 ]
Bien, Ewa [9 ]
Ociepa, Tomasz [10 ]
Wawrykow, Pawel [11 ]
Tomaszewska, Renata [12 ]
Plonowski, Marcin [13 ]
Pierlejewski, Filip [14 ]
Gamrot-Pyka, Zuzanna [15 ]
Malas, Zofia [16 ]
Urbanek-Dadela, Agnieszka [17 ]
Stolpa, Weronika [18 ]
Zaucha-Prazmo, Agnieszka [19 ]
Gozdzik, Jolanta [20 ]
Chaber, Radoslaw [21 ]
Gil, Lidia [22 ]
Styczynski, Jan [1 ]
机构
[1] Nicolaus Copernicus Univ Torun, Dept Pediat Hematol & Oncol, Coll Med, Ul Sklodowskiej Curie 9, PL-85094 Bydgoszcz, Poland
[2] Nicolaus Copernicus Univ Torun, Dept Pediat Surg, Coll Med, Bydgoszcz, Poland
[3] Med Univ, Dept Pediat Stem Cell Transplantat Hematol & Onco, Wroclaw, Poland
[4] Med Univ, Dept Pediat Hematol & Oncol, Warsaw, Poland
[5] Univ Med Sci, Dept Pediat Oncol Hematol & Transplantol, Poznan, Poland
[6] Childrens Mem Hlth Inst, Dept Oncol, Warsaw, Poland
[7] Nicolaus Copernicus Univ Torun, Dept Microbiol, Coll Med, Bydgoszcz, Poland
[8] Jagiellonian Univ, Dept Pediat Oncol & Hematol, Univ Childrens Hosp, Coll Med, Krakow, Poland
[9] Med Univ, Dept Pediat Hematol & Oncol, Gdansk, Poland
[10] Pomeranian Med Univ, Dept Pediat Hematooncol & Gastroenterol, Szczecin, Poland
[11] Pomeranian Med Univ, Dept Pediat Oncol, Szczecin, Poland
[12] Silesian Med Univ, Dept Pediat Hematol & Oncol, Zabrze, Poland
[13] Med Univ, Dept Pediat Oncol & Hematol, Bialystok, Poland
[14] Med Univ, Dept Pediat Oncol Hematol & Diabetol, Lodz, Poland
[15] Chorzow Pediat & Oncol Ctr, Div Pediat Hematol & Oncol, Chorzow, Poland
[16] Children Hosp, Div Pediat Hematol & Oncol, Olsztyn, Poland
[17] Children Hosp, Div Pediat Hematol & Oncol, Kielce, Poland
[18] Silesian Med Univ, Dept Pediat, Div Pediat Oncol Hematol & Chemotherapy, Katowice, Poland
[19] Med Univ, Dept Pediat Hematol Oncol & Stem Cell Transplanta, Lublin, Poland
[20] Jagiellonian Univ, Dept Clin Immunol & Transplantol, Univ Childrens Hosp, Stem Cell Transplant Ctr,Coll Med, Krakow, Poland
[21] Univ Rzeszow, Dept Pediat Oncohematol, Rzeszow, Poland
[22] Univ Med Sci, Dept Hematol & Transplantol, Poznan, Poland
关键词
bacterial infections; children; hematopoietic stem cell transplantation; invasive fungal infections; malignant diseases; oncohematology; viral infections; 4TH EUROPEAN CONFERENCE; HEMATOLOGICAL MALIGNANCIES; PEDIATRIC-PATIENTS; LEUKEMIA ECIL-4; INFECTIONS; GUIDELINES; FLUCONAZOLE; POSACONAZOLE; PREVENTION; MANAGEMENT;
D O I
10.1111/myc.12990
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The objective of the study was the analysis of incidence and outcome of invasive fungal disease (IFD) in children treated for malignancy (PHO, paediatric hematology-oncology) or undergoing hematopoietic cell transplantation (HCT) over a period of six consecutive years in nationwide study. A total number of 5628 patients with newly diagnosed malignancies and 971 patients after HCT (741 allo-HCT and 230 auto-HCT) were screened for infectious complications in biennial reports. IFD incidence was lower among PHO patients: 8.8% vs 21.2% (P < .0001) and survival from IFD was better: 94.2% vs 84.1% (P < .0001). Auto-HCT patients had lower incidence (10.9% vs 24.4%) and lower mortality than allo-HCT patients. Introduction of national antifungal prophylaxis programme in HCT and acute leukaemia patients decreased incidence of IFD in HCT (from 23.1% to 13.4%) and AML on conventional chemotherapy (from 36% to 23%) but not in ALL patients during chemotherapy. In multivariate analysis, the incidence of IFD was higher in patients after HCT, diagnosed for ALL, AML or NHL, and in patients > 10 years old. Factors contributing to death with infection were as follows: undergoing HCT, diagnosis of acute leukaemia (ALL or AML) and duration of treatment of infection > 21 days. In conclusion, the incidence of IFD in allo-HCT and in AML patients on chemotherapy has decreased after introduction of national programme of antifungal prophylaxis, while the incidence of IFD in ALL patients on chemotherapy did not change significantly. The outcome of IFD both in PHO and HCT patients has largely improved in comparison with historical international data.
引用
收藏
页码:990 / 998
页数:9
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