异基因造血干细胞移植术后侵袭性真菌感染的流行病学：单中心12年研究结果

Invasive fungal infection in allogeneic hematopoietic stem cell transplant recipients: single center experiences of 12 years 异基因造血干细胞移植术后侵袭性真菌感染的流行病学：单中心12年研究结果 first-author corresp ‡Corresponding Author ‡Corresponding Author †E-mail:huanghe@zju.edu.cn †E-mail:huanghe@zju.edu.cn huanghe@zju.edu.cn Bone Marrow Transplantation Center, the First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, China Bone Marrow Transplantation Center, the First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, China Invasive fungal infection (IFI) is a growing cause of morbidity and mortality among patients after allogeneic hematopoietic stem cell transplantation (allo-HSCT). We retrospectively reviewed the records of 408 patients undergoing allo-HSCTs during the period November 1998 to December 2009, analyzed the incidence and risk factors of IFI, and examined the impact of IFI on overall survival. A total of 92 (22.5%) episodes suffered proven or probable IFI (4 patients were proven, 88 patients were probable). Candida was the most common pathogen for early IFI, and mold was the most frequent causative organism for late IFI. A prior history of IFI, human leukocyte antigen (HLA) mismatch, long-time neutropenia, and acute graft-versus-host-disease (GVHD) were risk factors for early IFI. A prior history of IFI, corticosteroid therapy, cytomegalovirus (CMV) disease, and chronic GVHD were risk factors for late IFI. IFI-related mortality was 53.26%. The 12-year overall survival (OS) rate for IFI was significantly lower than that of patients without IFI (41.9% vs. 63.6%, P < 0.01). 目的 2 回顾性分析了浙江大学医学院附属第一医院骨髓移植中心1998年至2009年接受造血干细胞移植（HSCT）发生侵袭性真菌感染（IFI）的患者资料，评估HSCT后IFI发病情况、流行病学特征及危险因素，以期寻找病原菌特点及相关的危险因素，为制定更有针对性的预防治疗策略提供依据。 创新点 2 首次对本中心异基因HSCT后的IFI感染情况进行统计分析，研究年限长，样本量较大；另作为国内较成熟的移植中心之一，本中心的研究结果对国内异基因HSCT后IFI感染情况有较大的参考意义。 方法 2 对1998年11月至2009年12月在本移植中心接受异基因HSCT的408例患者进行观察分析，总结HSCT后IFI发病情况和病原菌分布，并采用多因素分析判断危险因素。 结论 2 本研究显示IFI与HSCT预后明显相关，HSCT后不同时期IFI病原菌分布及危险因素存在差异。临床应根据IFI病原学特点及HSCT后时间分布特点，采取不同的策略，更有针对性地用药及开始治疗，从而改善预后。 Invasive fungal infection Allogeneic hematopoietic stem cell transplantation Incidence Risk factors 侵袭性真菌感染 异基因造血干细胞移植 危险因素 Introduction 1 Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is an effective and sometimes the only curative therapy for patients with high-risk hematologic malignancies. Due to the therapies preventing and treating graft-versus-host-disease (GVHD) and cytopenia, HSCT recipients have a high risk of acquiring invasive fungal infection (IFI) (Jantunen et al., 1997 1997 ; Bjorklund et al., 2007 2007 ). Over the past decades, multiple changes in transplant procedures and antifungal prophylaxis have affected the epidemiology of IFI (Neofytos et al., 2009 2009 ; Kontoyiannis et al., 2010 2010 ). Although fluconazole prophylaxis has reduced the incidence of IFI caused by Candida albicans , it resulted in a subsequent increase in resistant candidiasis, such as Candida glabrata and Candida krusei . Aspergillus has become the most frequent organism and other infections caused by molds, such as Zygomycetes and Fusariums , also have increased since the 1990s (Neofytos et al., 2009 2009 ). Previously identified risk factors of IFI include donor type, GVHD, high-dose corticosteroids, increased ferritin levels, and so on (Fukuda et al., 2003 2003 ; Thursky et al., 2004 2004 ; Ozyilmaz et al., 2010 2010 ; Omer et al., 2013 2013 ). Epidemiology and risk factors of IFI differ due to the changes in antifungal prophylaxis and treatment in different regions. Exploring these differences may improve management strategies and study design for allo-HSCT recipients. Here in our study, we retrospectively reviewed 408 consecutive patients who underwent allo-HSCT between 1998 and 2009 in our center, identified the incidence and risk factors of IFI, and calculated the outcomes. Subjects and methods 1 Patients and donors 2 We collected a total of 408 patients, 251 males and 157 females aged 8–52 years (a median age of 28 years), who underwent allo-HSCT in our center between November 1998 and December 2009. According to the French-American-British (FAB) criteria, 127 (31.13%) cases were acute myeloid leukemia (AML), 120 (29.41%) were acute lymphocytic leukemia (ALL), 127 (31.13%) were chronic myeloid leukemia (CML), and 34 (8.33%) were other hematologic diseases. Among the allogenic HSCT recipients, 195 (47.79%) received bone marrow transplantation (BMT), whereas 213 (52.21%) received peripheral blood stem cells (PBSCs) with a granulocyte colony-stimulating factor (G-CSF) mobilized. Donors were human leukocyte antigen (HLA)-matched ( n =298), HLA-mismatched ( n =82), or HLA haploidentical-matched ( n =28). Clinical characteristics of the entire cohort are presented in Table 1 1 . Data are expressed as n (%), except for recipient age (median (range)) and gender (male/female) IFI: invasive fungal infection; ALL: acute lymphocytic leukemia; AML: acute myeloid leukemia; CML: chronic myeloid leukemia; MDS: myelodysplastic syndrome; NHL: non-Hodgkin’s lymphoma; MM: multiple myeloma; PNH: paroxysmal nocturnal hemoglobinuria; MAL: mixed acute leukemia; HLA: human leukocyte antigen; ATG: anti-thymocyte immunoglobuline 2 Parameter 2 Total 3 IFI Yes No P Recipient age (year), median (range) 28.96 (8–52) 28.91 (9–50) 28.97 (8–52) 0.45 Gender, male/female 251/157 62/30 189/127 0.14 Underlying disease 0.47  ALL 120 (29.41) 37 (30.83) 83 (69.17)  AML 127 (31.13) 26 (20.47) 101 (79.53)  CML 127 (31.13) 21 (16.54) 106 (83.46)  MDS/AML 21 (5.15) 5 (23.81) 16 (76.19)  NHL 3 (0.74) 0 (0.00) 3 (100.00)  MM 3 (0.74) 1 (33.33) 2 (66.67)  PNH 1 (0.25) 0 (0.00) 1 (100.00)  MAL 6 (1.47) 2 (33.33) 4 (66.67) Donor type 0.24  Related 164 (40.20) 30 (18.29) 134 (81.71)  Unrelated 244 (59.80) 62 (25.41) 182 (74.59) Stem cell source 0.25  Bone marrow 195 (47.79) 39 (20.00) 156 (80.00)  Peripheral blood 213 (52.21) 53 (24.88) 160 (75.12) HLA 0.03  Matched 298 (73.04) 58 (19.46) 240 (80.54)  Mismatched 110 (26.96) 34 (30.91) 76 (69.09) 2 Conditioning regimen 0.68  Without ATG 342 (83.82) 77 (22.51) 265 (77.49)  With ATG 66 (16.18) 15 (22.73) 51 (77.27) Transplant procedure 2 A total of 349 (85.54%) patients received myeloablative conditioning regimens composed of busulfan (BU) plus cyclophosphamide (CY). The 27 (6.62%) patients who received HLA haploidentical transplants received BU/CY/cytosine arabinoside (Ara-C)/1-(2-chloroethyl)-3-(4-methylcyclohexyl)-1-nitrosourea (methyl-CCNU)/anti-thymoglobin (ATG). Reduced-intensity conditioning regimens which were predominantly fludarabine-based combinations were used in 32 cases. In addition, 66 (16.18%) individuals with HLA-mismatched donors received ATG as part of their conditioning regimen. GVHD prophylaxis and therapy 2 In both unrelated and sibling transplantation cohorts, patients received the same GVHD prophylaxis regimen consisting of cyclosporine, mycophenolate mofetil, and short-term methotrexate (MTX). Acute GVHD was graded from 0 to IV according to established criteria. Patients who survived for >100 d were determined as chronic GVHD, which was graded as limited or extensive. Acute GVHD was treated with high-dose methyl-prednisolone (MP), and ATG was used for patients refractory to MP. Supportive care 2 All patients were cared for in rooms with high-efficiency particulate air filters. Empiric antibacterial agents for fever and cotrimoxazole as pneumocystis prophylaxis were administered. For the prophylaxis of cytomegalovirus (CMV), ganciclovir or foscarnet sodium was used before transplantation and acyclovir combined with immunoglobulin after transplantation. Definition, prophylaxis, and therapy of IFI 2 IFI was defined as proven or probable according to the European Organization for Research and Treatment of Cancer/Mycoses Study Group (EORTC/MSG) criteria (Ascioglu et al., 2002 2002 ). Proven fungal infection required histopathologic findings from biopsied tissues or culture of sterile tissue. Probable infection was considered when patients had both clinical criteria and at least one microbiologic criterion (fungus was identified from sputum or bronchoalveolar lavage fluid). Infections were classified according to occurrence timing after transplantation: early IFI (≤100 d after transplantation) and late IFI (Group I: 100‒180 d; Group II: > 180 d after transplantation). From November 1998 to December 2007, fluconazole (400 mg/d, oral (p.o.)) was given to all HSCT recipients from Day–7 to Day+90 post-HSCT, with dosages adjusted on the basis of their renal function. After January 2008, patients with a history of IFI pre-HSCT received itraconazole (200 mg/d, intravenous (i.v.)) during neutropenia ( < 1.0×10 9 L −1 ), and were changed to oral fluconazole or itraconazole after neutrophil recovery ( > 1.0×10 9 L −1 ). Patients with persistent fever refractory to broad-spectrum antibiotic treatment were also provided with antifungal therapy, usually itraconazole, caspofungin, voriconazole, or amphotericin B. Statistical methods 2 Continuous variables were compared between groups using Student’s t test or Wilcoxon rank sum test. The Chi-square test or Fisher’s test was used for categorical variables. Univariate analysis and multivariate analysis were performed, and Cox proportional hazard models were estimated to assess risk factors for IFI and survival rate. Kaplan-Meier estimates were computed for survival, and a stratified log-rank test was used to compare these groups. P < 0.05 was considered significant. All analyses were conducted using SAS 9.2 and ATATA 11.0. Results 1 Clinical outcomes after allo-HSCT 2 Clinical outcomes after allo-HSCT among 408 patients were analyzed and summarized in Table 2 2 . The median follow-up period was 28 (range 1–145) months. All patients achieved hematopoietic reconstitution, with neutrophil engraftment ( > 0.5×10 9 L −1 ) on Day+14 (range+7–+31 d) and platelet engraftment ( > 20×10 9 L −1 ) on Day+18 (range+8–+144 d). The cumulative incidence rates of acute GVHD Grades I to II and Grades III to IV were 35.5% and 8.1%, respectively. The cumulative incidence of chronic GVHD was 39.2% (29.9% limited and 9.3% extensive). Positive CMV antigenemia was observed in 35.5% of the recipients. Thirty-nine patients developed CMV disease, including pneumonia, enteritis, and cystitis. Data are expressed as n (%), except for day for engraftment (median (range)) IFI: invasive fungal infection; ANC: absolute neutrophil count; PLT: platelet; GVHD: graft-versus-host-disease; aGVHD: acute GVHD; cGVHD: chronic GVHD; CMV: cytomegalovirus 2 Parameter 2 Total 3 IFI Yes No P Day for engraftment  ANC > 0.5×10 9 L −1 14 (7–31)  PLT > 20×10 9 L −1 18 (8–144) aGVHD <0.001  Grades I–II 145 (35.54) 49 (33.79) 96 (66.21)  Grades III–IV 33 (8.09) 12 (36.36) 21 (63.64) cGVHD <0.001  Limited 122 (29.90) 32 (26.23) 90 (73.77)  Extensive 38 (9.31) 22 (57.89) 16 (42.11) CMV <0.001  CMV viremia 144 (35.29) 42 (29.17) 102 (70.83)  CMV disease 39 (9.56) 17 (43.59) 22 (56.41) Incidence and clinical features of IFI 2 We detected 92 (22.5%) episodes of IFI in patients after allo-HSCT, with 4 proven cases and 88 probable IFI cases. The median age of these patients was 29 (range 9–50) years. Among the 92 cases, 69% were males. The cumulative incidence rates of IFI for 100 d, 6 months, and 1 year were 7.87%, 5.77%, and 12.60%, respectively (Fig. 1 1 ). Candidiasis was responsible for 50 proven and probable episodes (54.35%), and mold infection for 42 episodes (45.65%). Non-albicans caused 52% (26/50) of candidiasis. Among mold infection, Aspergillus was associated with 76.19% (32/42) cases (Fig. 2 2 ). The median time after allo-HSCT to onset of IFI was 140 (range 30–598) d for invasive candidiasis infection (ICI) and 243 (range 12–2461) d for invasive mold infection (IMI). There was a trend for ICI to occur earlier post-HSCT than IMI. The lung was the most frequently affected site (69.6%, 64/92), followed by oropharynx (14.1%, 13/92), gastrointestinal tract (9.8%, 9/92) and urinary tract (10.9%, 10/92), blood (3.3%, 3/92), and skin (1%, 1/92), and eight cases had more than one site affected. The cumulative incidence rates of IFI for 100 d, 6 months, and 1 year were 7.87%, 5.77%, and 12.60%, respectively According to the timing after allo-HSCT, 27 (29.35%) cases were diagnosed as early IFI (≤100 d) and 65 (70.65%) cases were diagnosed as late IFI ( > 100 d), of which 43 (66.15%) developed later than 180 d after transplantation. Candida accounted for 66.67% (18/27) and 49.23% (32/65) of early and late IFIs, respectively. However, this difference did not reach statistical significance. We further grouped late IFI to Group I ( < +180 d) and Group II ( > +180 d), revealing that the probability of Candida among Group I was significantly higher than that among Group II (72.72% vs. 37.21%; Fig. 2 2 ). Risk factors for IFI 2 Risk factors by univariate analysis for the development of IFI during each time period are presented in Table 3 3 . HLA mismatch, sustained neutropenia ( < 0.5×10 9 L −1 ) lasting > 2 weeks, CMV infection, and severe acute GVHD were significant risk factors for early IFI. Chronic GVHD and CMV disease increased risk for late IFI. A prior history of IFI and corticosteroid therapy associated with increased risk for both early and late IFIs. Age, gender, underlying disease, and conditioning regimen were not significant. Data are expressed as n (%), expect for age (mean±standard deviation) IFI: invasive fungal infection; ALL: acute lymphocytic leukemia; AML: acute myeloid leukemia; CML: chronic myeloid leukemia; MDS: myelodysplastic syndrome; NHL: non-Hodgkin’s lymphoma; MM: multiple myeloma; PNH: paroxysmal nocturnal hemoglobinuria; MAL: mixed acute leukemia; BMT: bone marrow transplantation; PBSCT: peripheral blood stem cell transplantation; HLA: human leukocyte antigen; ATG: anti-thymocyte immunoglobuline; GVHD: graft-versus-host-disease; aGVHD: acute GVHD; cGVHD: chronic GVHD; CMV: cytomegalovirus; Ref: reference 2 Risk factor 3 Early IFI ( n =27) 3 Late IFI ( n =65) n (percentage) * * HR 95% CI n (percentage) * * HR 95% CI Age (year) 30.19±9.63 1.06 0.88–1.29 27.62±10.05 0.94 0.83–1.06 Gender  Male 15 (24.19) Ref Ref 47 (75.81) Ref Ref  Female 12 (40.00) 1.18 0.55–2.52 18 (60.00) 0.60 0.35–1.03 Underlying disease  ALL 11 (29.73) Ref Ref 26 (70.27) Ref Ref  AML 8 (30.77) 0.62 0.25–1.55 18 (69.23) 0.58 0.32–1.05  CML 6 (28.57) 0.45 0.16–1.20 15 (71.43) 0.48 0.25–0.90  MDS/AML 1 (20.00) 0.48 0.06–3.70 4 (80.00) 0.75 0.26–2.16  NHL 0 (0.00) 0 (0.00)  MM 0 (0.00) 1 (100) 1.28 0.17–9.43  PNH 0 (0.00) 0 (0.00)  MAL 1 (50.00) 1.99 0.26–15.43 1 (50.00) 0.77 0.11–5.71 Previous IFI 15 (39.47) 8.94 4.18–19.13 23 (60.53) 3.69 2.22–6.14 Donor type  Related 9 (30.00) Ref Ref 21 (70.00) Ref Ref  Unrelated 18 (29.03) 1.46 0.66–3.25 44 (70.97) 1.49 0.89–2.50 Stem cell source  BMT 14 (35.90) Ref Ref 25 (64.10) Ref Ref  PBSCT 13 (24.53) 0.91 0.43–1.94 40 (75.47) 1.48 0.90–2.44 HLA  Matched 15 (25.86) Ref Ref 43 (74.14) Ref Ref  Mismatched 12 (35.29) 2.47 1.16–5.28 22 (64.71) 1.58 0.95–2.65 Conditioning regimen  Without ATG 24 (31.17) Ref Ref 53 (68.83) Ref Ref  With ATG 3 (20.00) 0.66 0.20–2.20 12 (80.00) 1.18 0.63–2.21 Neutropenia  <2 weeks 12 (20.00) Ref Ref 48 (80.00) Ref Ref  >2 weeks 15 (46.88) 2.44 1.14–5.23 17 (53.12) 0.75 0.43–1.30 aGVHD  Grades I–II 11 (22.45) 2.40 0.99–5.79 38 (77.55)  Grades III–IV 7 (58.33) 6.74 2.51–18.12 5 (41.67) cGVHD  Limited 9 (8.13) 23 (91.87) 2.49 1.37–4.53  Extensive 0 (0.00) 22 (100) 8.19 4.46–15.04 CMV  CMV viremia 12 (28.57) 2.40 1.01–5.69 30 (71.43) 2.18 1.27–3.72  CMV disease 6 (35.29) 5.33 1.90–14.98 11 (64.71) 3.68 1.80–7.51 Corticosteroids  0 12 (42.86) Ref Ref 16 (57.14) Ref Ref  <1.0 mg/(kg∙d) 3 (16.67) 0.76 0.21–2.70 15 (83.33) 2.67 1.32–5.41  1.0–1.9 mg/(kg∙d) 5 (17.86) 4.76 1.68–13.52 23 (82.14) 12.36 6.51–23.44  ≥2.0 mg/(kg∙d) 7 (38.89) 4.73 1.86–12.03 11 (61.11) 5.13 2.38–11.05 Multivariate analyses showed previous history of IFI (hazard ratio (HR)=9.53; 95% confidence interval (CI), 4.05–22.44), HLA mismatch (HR=2.55; 95% CI, 1.07–6.06), sustained neutrophil > 2 weeks (HR=1.94; 95% CI, 1.03–4.56), and Grades III to IV acute GVHD (HR=2.46; 95% CI, 1.01–12.46) were significant for early IFI. A prior history of IFI (HR=2.62; 95% CI, 1.46–4.72), CMV disease (HR=3.80; 95% CI, 1.71–8.42), limited and extensive chronic GVHD (HR=2.84; 95% CI, 1.52–5.30 and HR=3.21; 95% CI, 1.54–6.68, respectively) demonstrated a higher mortality risk for late IFI. The impact of corticosteroids for late IFI depended on the dosage. Corticosteroids of < 1.0 mg/(kg∙d) did not increase risk of developing IFI. Conversely, corticosteroids with a dosage of ≥1.0 mg/(kg∙d) affected IFI in the late period (Table 4 4 ). IFI: invasive fungal infection; HLA: human leukocyte antigen; GVHD: graft-versus-host-disease; aGVHD: acute GVHD; cGVHD: chronic GVHD; CMV: cytomegalovirus; Ref: reference 2 Risk factor 2 Early IFI ( n =27) 2 Late IFI ( n =65) HR 95% CI HR 95% CI Previous IFI 9.53 4.05–22.44 2.62 1.46–4.72 HLA  Matched Ref Ref  Mismatched 2.55 1.07–6.06 Neutropenia  <2 weeks Ref Ref  >2 weeks 1.94 1.03–4.56 aGVHD  Grades I‒II 1.82 0.69–4.81  Grades III‒IV 2.46 1.01–12.46 cGVHD  Limited 2.84 1.52–5.30  Extensive 3.21 1.54–6.68 CMV  CMV viremia 1.20 0.45–3.21 1.13 0.63–2.03  CMV disease 2.88 0.92–8.95 3.80 1.71–8.42 Corticosteroids  0 Ref Ref Ref Ref  <1.0 mg/(kg∙d) 0.77 0.22–2.73 1.80 0.87–3.73  1.0–1.9 mg/(kg∙d) 2.06 0.58–7.27 5.50 2.45–12.34  ≥2.0 mg/(kg∙d) 1.05 0.23–4.85 2.74 1.14–6.64 Outcomes 2 IFI-related mortality was 49 out of 92 cases (53.26%) of IFI. The 12-year overall survival (OS) rate for IFI was 41.9%, with significant differences when compared with patients without IFI (63.6%, P < 0.001; Fig. 3a 3a ). Late IFI was associated with a significantly higher 12-year OS compared with early IFI (Fig. 3b 3b ). For patients with only one IFI, the 12-year OS was better for patients with Candida when compared with molds (Fig. 3c 3c ). (a) The overall survival for all 408 patients with or without IFI; (b) Overall survival for 27 patients with development of early IFI and 65 patients with late IFI; (c) Overall survival for patients with Candida infection and mold infection Discussion 1 Despite considerable progress in the management of the complications of HSCT, infection remains an important cause of post-transplant morbidity and mortality, primarily after allogeneic HSCT. European Group for Blood and Marrow Transplantation (EBMT) analyzed a large homogeneous group of 14 403 patients transplanted for early leukemia from an HLA-identical sibling and cause of infection death after allogeneic HSCT (Gratwohl et al., 2005 2005 ). Survival increased from 52% at 5 years in the first to 62% in the third cohort ( P < 0.05), and treatment-related mortality decreased from 36% to 26% ( P < 0.05) due to a reduction in death from infection ( P < 0.01). IFI is an important cause of post-transplant mortality. The incidence rate of IFI has been reported to be 10%‒26% in HSCT recipients (Koldehoff and Zakrzewski, 2005 2005 ; Post et al., 2007 2007 ), with mortality ranging from 40% to 90% (Lin et al., 2001 2001 ; Dagenais and Keller, 2009 2009 ). We performed this 12-year retrospective study to evaluate the epidemiologic characteristics, clinical manifestation and outcomes of IFI in 408 allogenic HSCT recipients. We report that patients with IFI have a lower 12-year OS than those without IFI (41.9% vs. 63.6%, P < 0.01), reflecting the fact that IFI has a significant impact on long-term survival of transplant patients. Over the past two decades, changes in transplantation practices and strategies to diagnose and treat IFI have likely impacted the epidemiology of IFI. According to the data from the Transplant Associated Infections Surveillance Network, a network of 23 US transplant centers, invasive aspergillosis (43%), invasive candidiasis (28%), and zygomycosis (8%) are the most common IFIs. Aspergillus fumigatus causes 44% of aspergillosis, and Candida glabrata is the most common organism (33%) causing invasive candidiasis (Kontoyiannis et al., 2010 2010 ). In our previous study, we performed CT-guided percutaneous lung biopsy in 16 patients who were initially suspected of developing fungal infection. Ten out of the 16 patients (62.5%) were diagnosed with a fungal infection (8 with Aspergillus , 2 with mold fungus). All of the 10 cases had mold infection, and the incidence of Aspergillus infection was 80% (Shi et al., 2009 2009 ). The observed results in our study are not entirely consistent with the prior studies. According to our data, candidiasis was more prevalent than mold infections (54.35% vs. 45.65%). Among the candidiasis cases, Candida albicans was the most common pathogen (28%), followed by Candida glabrata (18%) and Candida tropicalis (14%). The rate of mold infections was lower than that reported in our previous study (Shi et al., 2009 2009 ), which may be explained by the following reasons. All patients underwent CT-guided lung biopsies in our previous prospective study, providing higher diagnostic accuracy than blood and sputum culture, while only 4 patients underwent biopsies in this retrospective study. Also, patients who received lung biopsies were highly suspected of Aspergillus infection based on imaging findings, probably leading to an increased rate of Aspergillus infection. Additionally, the small number of patients (16 cases) may also amplify the positive rate of mold infection. Although Candida was presented as the most common pathogen in our center, there seemed to be a trend toward higher numbers of non-albicans and molds due to routine prophylaxis with fluconazole. This serves as a reminder to choose broad-spectrum antibiotics covering non-albicans and molds in the treatment of post-HSCT fungal infections. Since only a small number of patients were treated with voriconazole in our study, we observed no voriconazole-resistant species (e.g. Zygomycetes ). Previous studies have noted that IFI primarily occurs in the phase of hematopoietic reconstitution, generally two to three months after transplantation. Candida is the most common pathogen of early IFI, while mold is the most common pathogen of late IFI. In patients who also developed GVHD, IFI may occur at three to six months and even later (Koldehoff and Zakrzewski, 2005 2005 ; Garcia-Vidal et al., 2008 2008 ). Our data demonstrate that the median time for the development of ICI is earlier than that for IMI (140 d vs. 243 d, P < 0.05), reflecting the fact that mold infections are more common in the late period after HSCT. The incidences of mold and Candida infections in early and late IFIs differed, but did not reach statistical significance. We further evaluated the incidence rate of very late IFI and found that mold infections significantly increased ( P < 0.05). These findings highlight the importance of strengthening the detection and treatment of mold in the late period after transplantation. Multiple factors reported to be associated with the risk of IFI include donor type, conditioning regimens, prolonged neutropenia, GVHD, and high-dose corticosteroids (Fukuda et al., 2003 2003 ; Thursky et al., 2004 2004 ; Ozyilmaz et al., 2010 2010 ; Omer et al., 2013 2013 ). According to our data, we found similar risk factors infecting IFI. However, when we further analyzed the risk factors for each phase of IFI, we were able to demonstrate that there is a difference between the early and late IFIs. Despite the widespread use of cyclosporine, tacrolimus, mycophenolate mofetil, and other drugs for prophylaxis of GVHD in HSCT recipients, 25% to 45% of patients still developed Grades II to IV acute GVHD. HLA-mismatched recipients are at a particularly high risk for acute GVHD, which is the most likely cause of the high risk for IFI, especially for early IFI. Enhancing the immune inhibitors or increasing the dosage of corticosteroids may effectively control GVHD, while increasing the risk of IFI. In our study, univariate analysis showed that corticosteroid therapy is a risk factor during all periods. When further introduced into multivariate analyses, corticosteroid therapy only accounted for late IFI. This result suggests that long-term use of corticosteroids has a more advanced effect on late IFI. CMV is associated with development of IFI in both the early and the late post-transplant phases (Marr et al., 2002 2002 ). The mechanism remains unclear. The immune-modulating effect of CMV may be one of the explanations. In our study, CMV infection was the risk factor for early IFI in univariate analysis but not in multivariate analyses. CMV disease rather than CMV infection was associated with the risk of late IFI. This may be because CMV mostly occurs in the late period after transplantation. Strengthening serum monitoring of CMV and timely prevention of CMV may reduce the incidence of IFI, particularly late IFI. Prolonged neutropenia is a risk factor for IFI (Hovi et al., 2000 2000 ). Neutrophils play an important role in the defense against IFI. Our results showed that prolonged neutropenia, which generally occurs in the early period after transplantation, is a risk factor for early IFI but not for late IFI. It is important to recognize that the risks for IFI also depend on changes in the conditioning regimens, supportive care strategies, and therapy strategies. This study attempts to analyze the impact of conditioning regimens of IFI, such as myeloablative and non-myeloablative regimens, as well as conditioning regimens with or without ATG. Unfortunately we cannot draw convincing conclusions due to the small number of cases. Further work will be needed to assess the association between conditioning regimen and IFI. It should be noted that our study has some limitations. Firstly, incidence of IFI can be lower than the actual incidence because of the strict definition of IFI (our study did not include possible IFI cases). Secondly, some patients with IFI may be misplaced into the control group, thus the significance of the difference between the two groups may be diluted. What is more, 125 of the total 408 patients participated in clinical trials of secondary prophylaxis during the study period, and patients with a history of IFI pre-HSCT received itraconazole (200 mg/d, i.v.) during neutropenia ( < 1.0×10 9 L −1 ), and changed to oral fluconazole or itraconazole after neutrophil recovery ( > 1.0×10 9 L −1 ), which in part may reduce the incidence of IFI after HSCT. References S Ascioglu , JH Rex , B de Pauw , 等 . Defining opportunistic invasive fungal infections in immunocompromised patients with cancer and hematopoietic stem cell transplants: an international consensus . Clin Infect Dis , 2002 . 34 ( 1 ): 7 - 14 . 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All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2008 (5). Informed consent was obtained from all patients for being included in the study. Additional informed consent was obtained from all patients for which identifying information is included in this article. 10.1631/jzus.B1500005 Project supported by the National Natural Science Foundation of China (Nos. 81170526 and 81270640) 2015-01-04 2015-08-17 2015-06-09 2022-01-05 Copyright © Zhejiang University and Springer-Verlag Berlin Heidelberg 2015 2015 Journal of Zhejiang University-SCIENCE B (Biomedicine and Biotechnology) 09 16