Incidence and risk factors of post-engraftment invasive fungal disease in adult allogeneic hematopoietic stem cell transplant recipients receiving oral azoles prophylaxis

被引:37
|
作者
Montesinos, P. [1 ]
Rodriguez-Veiga, R. [1 ]
Boluda, B. [1 ]
Martinez-Cuadron, D. [1 ]
Cano, I. [1 ]
Lancharro, A. [1 ]
Sanz, J. [1 ]
Arilla, M. J. [1 ]
Lopez-Chulia, F. [1 ]
Navarro, I. [1 ]
Lorenzo, I. [1 ]
Salavert, M. [2 ]
Peman, J. [3 ]
Calvillo, P. [4 ]
Martinez, J. [1 ]
Carpio, N. [1 ]
Jarque, I. [1 ]
Sanz, G. F. [1 ]
Sanz, M. A. [1 ,5 ]
机构
[1] Hosp Univ & Politecn La Fe, Dept Hematol, Valencia 46026, Spain
[2] Hosp Univ & Politecn La Fe, Dept Infect Dis, Valencia 46026, Spain
[3] Hosp Univ & Politecn La Fe, Dept Microbiol, Valencia 46026, Spain
[4] Hosp Univ & Politecn La Fe, Dept Radiol, Valencia 46026, Spain
[5] Univ Valencia, Dept Med, Valencia, Spain
关键词
ANTIFUNGAL PROPHYLAXIS; COMPETING RISK; INFECTION; ASPERGILLOSIS; VORICONAZOLE; EPIDEMIOLOGY; ITRACONAZOLE; FLUCONAZOLE; SCT; MULTICENTER;
D O I
10.1038/bmt.2015.181
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Studies that analyze the epidemiology and risk factors for invasive fungal disease (IFD) after engraftment in alloSCT are few in number. This single-center retrospective study included 404 alloSCT adult recipients surviving > 40 days who engrafted and were discharged without prior IFD. All patients who received >= 20 mg/day of prednisone were assigned to primary oral prophylaxis (itraconazole or low-dose voriconazole). The primary end point was the cumulative incidence (CI) of probable/proven IFD using the European Organization for Research and Treatment of Cancer and Mycoses Study Group (EORTC/MSG) criteria. The independent prognostic factors after multivariate analyses were used to construct a post-engraftment IFD risk score. The 1-year CI of IFD was 11%. The non-relapse mortality was 40% in those developing IFD and 16% in those who did not. The intent-to-treat analysis showed that 17% of patients abandoned the assigned prophylaxis. Age > 40 years, >= 1 previous SCT, pre-engraftment neutropenia > 15 days, extensive chronic GVHD and CMV reactivation were independent risk factors. The post-engraftment IFD score stratified patients into low risk (0-1 factor, CI 0.7%), intermediate risk (2 factors, CI 9.9%) and high risk (3-5 factors, CI 24.7%) (P < 0001). The antifungal prophylaxis strategy failed to prevent post-engraftment IFD in 11% of alloSCT. Our risk score could be useful to implement risk-adapted strategies using antifungal prophylaxis after engraftment.
引用
收藏
页码:1465 / 1472
页数:8
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