Table 2

Preemptive therapy in the 2 randomization arms

ParameterWhole patient population
P
DNAemia armAntigenemia arm
No. of patients 89 89 na 
No. (%) of HCMV infected patients 30 (34) 37 (42) ns 
No. (%) of treated patients 16 (18) 28 (31) .037 
Median days (range) to start of antiviral therapy 56 (17-144) 45 (22-88) .032 
Median days (range) of first course of antiviral therapy 15 (6-35) 14 (5-39) ns 
No. (%) of relapsing HCMV infections 8/16 (50) 15/28 (54) ns 
No. (%) of treated relapses 3/16 (19) 10/28 (36) ns 
Median days (range) of relapse treatment 11 (7-52) 14 (7-49) ns 
Median days (range) of total antiviral therapy 17 (6-69) 17 (5-69) ns 
Median days (range) of total antiviral therapy:    
    in patients with grade 0-I acute GvHD 12 (6-20) 14 (7-66) ns 
    in patients with grade II-IV acute GvHD 20 (6-69) 23 (5-69) ns 
        P grade 0-I vs grade II-IV (0.08) (ns) na 
ParameterWhole patient population
P
DNAemia armAntigenemia arm
No. of patients 89 89 na 
No. (%) of HCMV infected patients 30 (34) 37 (42) ns 
No. (%) of treated patients 16 (18) 28 (31) .037 
Median days (range) to start of antiviral therapy 56 (17-144) 45 (22-88) .032 
Median days (range) of first course of antiviral therapy 15 (6-35) 14 (5-39) ns 
No. (%) of relapsing HCMV infections 8/16 (50) 15/28 (54) ns 
No. (%) of treated relapses 3/16 (19) 10/28 (36) ns 
Median days (range) of relapse treatment 11 (7-52) 14 (7-49) ns 
Median days (range) of total antiviral therapy 17 (6-69) 17 (5-69) ns 
Median days (range) of total antiviral therapy:    
    in patients with grade 0-I acute GvHD 12 (6-20) 14 (7-66) ns 
    in patients with grade II-IV acute GvHD 20 (6-69) 23 (5-69) ns 
        P grade 0-I vs grade II-IV (0.08) (ns) na 

No patients from either arm contracted HCMV disease.

na indicates not applicable; ns, not significant.

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