Table 1.

Patient and transplantation characteristics of allogeneic transplant recipients after nonmyeloablative conditioning




Invasive mold infection
Factors
Total
Yes
No
Median patient age, y (range)   53 (0-72)   54 (25-67)   53 (0-72)  
Sex, M/F   107/56   15/10   92/46  
Underlying diagnosis, n (%)     
    Acute leukemia   25   4 (16)   21 (84)  
    CML   15   2 (13)   13 (87)  
    MDS/MPD   18   3 (17)   15 (83)  
    Lymphoma/CLL/myeloma   90   14 (16)   76 (84)  
    Other malignancy   8   2 (25)   6 (75)  
    Nonmalignancy   7   0 (0)   7 (100)  
Disease risk, n (%)*    
    High   82   12 (15)   70 (85)  
    Low   81   13 (16)   68 (84)  
Prior transplant, n (%)     
    Yes   52   8 (15)   44 (85)  
    No   111   17 (15)   94 (85)  
Conditioning, n (%)     
    2 Gy TBI   51   9 (18)   42 (82)  
    2 Gy TBI + fludarabine   112   16 (14)   96 (86)  
Donor, n (%)     
    HLA-matched related   108   20 (19)   88 (82)  
    HLA-matched unrelated   55   5 (9)   50 (91)  
Stem cell source, n (%)     
    PBSC   148   24 (16)   124 (84)  
    Bone marrow   15   1 (7)   14 (93)  
Season of transplant, n (%)     
    Winter   35   2 (6)   33 (94)  
    Spring   45   8 (18)   37 (82)  
    Summer   49   10 (20)   39 (80)  
    Fall   34   5 (15)   29 (85)  
CMV risk group, n (%)    
    Low   46   11 (24)   35 (76)  
    Intermediate   27   3 (11)   24 (89)  
    High
 
90
 
11 (12)
 
79 (88)
 



Invasive mold infection
Factors
Total
Yes
No
Median patient age, y (range)   53 (0-72)   54 (25-67)   53 (0-72)  
Sex, M/F   107/56   15/10   92/46  
Underlying diagnosis, n (%)     
    Acute leukemia   25   4 (16)   21 (84)  
    CML   15   2 (13)   13 (87)  
    MDS/MPD   18   3 (17)   15 (83)  
    Lymphoma/CLL/myeloma   90   14 (16)   76 (84)  
    Other malignancy   8   2 (25)   6 (75)  
    Nonmalignancy   7   0 (0)   7 (100)  
Disease risk, n (%)*    
    High   82   12 (15)   70 (85)  
    Low   81   13 (16)   68 (84)  
Prior transplant, n (%)     
    Yes   52   8 (15)   44 (85)  
    No   111   17 (15)   94 (85)  
Conditioning, n (%)     
    2 Gy TBI   51   9 (18)   42 (82)  
    2 Gy TBI + fludarabine   112   16 (14)   96 (86)  
Donor, n (%)     
    HLA-matched related   108   20 (19)   88 (82)  
    HLA-matched unrelated   55   5 (9)   50 (91)  
Stem cell source, n (%)     
    PBSC   148   24 (16)   124 (84)  
    Bone marrow   15   1 (7)   14 (93)  
Season of transplant, n (%)     
    Winter   35   2 (6)   33 (94)  
    Spring   45   8 (18)   37 (82)  
    Summer   49   10 (20)   39 (80)  
    Fall   34   5 (15)   29 (85)  
CMV risk group, n (%)    
    Low   46   11 (24)   35 (76)  
    Intermediate   27   3 (11)   24 (89)  
    High
 
90
 
11 (12)
 
79 (88)
 

N = 163; with invasive mold infection: n = 25 patients (15%); without invasive mold infection: n = 138 patients (85%)

*

Patients were stratified based on underlying disease, as described previously15 : high-risk was defined as active or de novo or relapsed acute myeloid leukemia (AML), myelodysplastic syndrome (MDS) (refractory anemia with excess of blasts or excess blasts in transformation), myeloproliferative disorder (MPD), acute lymphocytic leukemia (ALL), chronic lymphocytic leukemia (CLL), non-Hodgkin lymphoma (NHL), Hodgkin disease (HD), multiple myeloma (MM) regardless of status, accelerated phase or blastic crisis of chronic myeloid leukemia (CML), or renal cell carcinoma; low-risk was defined as nonmalignant diseases including immune deficiency syndrome, any of the above diseases with unknown disease status or in remission except for MM, CML chronic phase, and MDS (refractory anemia with or without ringed sideroblasts)

Classification of the CMV risk group was based on pretransplantation CMV serostatus14 : CMV low-risk (donor and recipient serologically negative), CMV intermediate-risk (donor serologically positive and recipient negative), and CMV high-risk (recipient positive and donor negative or positive)

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