Table 1.

Characteristics of study subjects

CharacteristicAll patientsEC (n = 13)SCs (n = 16)NCs (n = 13)P*P
Age, median (IQR), y 57 (48-63) 57 (46-61) 57 (51-62) 58 (46-65) .86 .91 
Male sex 26 (62) 7 (54) 10 (63) 9 (69) .79 >.99 
Follow-up, median (IQR), post-HCT days 511 (227-778) 373 (210-922) 602 (453-822) 529 (76-772) .48 .37 
Time to CMV reactivation, median (IQR), posttransplant days 30 (12-35) NA 34 (15-57) 18 (5-33) n/a .03 
CMV reactivation within 30 d posttransplant 12 (29) NA 6 (38) 6 (46) n/a .72 
Initial CMV DNAemia, median (IQR), IU/mL 106 (96-137) NA 102 (96-137) 106 (96-181) n/a .62 
Peak CMV DNAemia, median (IQR), IU/mL 377 (137-1800) NA 140 (137-192) 1,832 (1600-9189) n/a <.0001 
CMV DNAemia preceding therapy, median (IQR), IU/mL 873 (700-1500) NA n/a 873 (700-1500) n/a n/a 
Duration of CMV DNAemia, median (IQR), d 30 (22-40) NA 22 (5-32) 40 (30-60) n/a .0008 
CMV DNAemia lasting >7 d 24 (57) NA 11 (69) 13 (100) n/a .048 
Recurrent CMV DNAemia (ie, ≥2 episodes of viremia) 10 (26) NA 4 (25) 6 (60) n/a .11 
CMV disease 4 (9.5) 1 (6.3) 3 (23) .18 .29 
Underlying diagnosis       
 Leukemia 24 (57) 10 (77) 8 (50) 6 (46) .25 >.99 
 Lymphoma 6 (14) 1 (8) 1 (6) 4 (31) .22 .14 
 MDS/MPN 12 (29) 2 (15) 7 (44) 3 (23) .25 .43 
Conditioning regimen       
 Myeloablative§ 11 (26) 3 (23) 2 (13) 6 (46) .2 .1 
Stem cell source       
 Peripheral blood 41 (98) 13 (100) 16 (100) 12 (92) .62 .44 
 Bone marrow 1 (2) 1 (8)   
Type of donor       
 Unrelated 20 (48) 4 (31) 5 (31) 11 (85) .006 .008 
 HLA-matched related 22 (52) 9 (69) 11 (69) 2 (15)   
Malignancy status at time of transplant       
 Complete remission 26 (62) 9 (69) 9 (56) 8 (62) .92 >.99 
 Time to engraftment, median (IQR), d 10 (11-13) 11 (9-18) 11 (10-13) 12 (11-19) .49 .28 
 aGVHD (grade 2-4) 13 (31) 3 (23) 5 (31) 5 (38) .65 .71 
 Steroids (>0.5mg/kg), day 30 6 (14) 2 (15) 1 (6) 3 (23) .47 .29 
(D)onor/(R)ecipient CMV serostatus       
 D R+ 12 (29) 3 (23) 6 (38) 3 (23) .63 .45 
 D+ R+ 30 (71) 10 (77) 10 (62) 10 (77)   
CD34+ cells infused (1 × 106), median (IQR) 7.4 (5.8-9.4) 7.8 (6.7-12) 7.6 (6.5-10) 6.0 (3.5-7.3) .04 .045 
Charlson Comorbidity Score, median (IQR) 3 (2-5) 3 (2-4) 3 (2-5) 3 (2-7) .68 .49 
Lymphoid malignancy 11 (26) 5 (38) 1 (6) 5 (38) .06 .06 
Absolute lymphocyte count, day 30, cells/µL 800 (480-1380) 800 (350-1390) 950 (725-1623) 700 (250-1300) .35 .17 
Time to “day 30” sample collection, median (range), d 29 (27-31) 28 (25-31) 30 (28-32) 29 (27-31) .11 .15 
1-y bacterial or fungal invasive infections 8 (19) 2 (15) 1 (6) 5 (38) .13 .06 
100-d all-cause mortality 5 (12) 1 (8) 4 (31) .03 .03 
1-y all-cause mortality 9 (21) 2 (15) 2 (13) 5 (38) .25 .19 
3-y all-cause mortality 10 (24) 2 (15) 3 (19) 5 (38) .39 .41 
100-d NRM 3 (7) 1 (8) 2 (15) .28 .19 
1-y NRM 5 (12) 1 (8) 1 (6) 3 (23) .49 .29 
3-y NRM 5 (12) 1 (8) 1 (6) 3 (23) .49 .29 
CharacteristicAll patientsEC (n = 13)SCs (n = 16)NCs (n = 13)P*P
Age, median (IQR), y 57 (48-63) 57 (46-61) 57 (51-62) 58 (46-65) .86 .91 
Male sex 26 (62) 7 (54) 10 (63) 9 (69) .79 >.99 
Follow-up, median (IQR), post-HCT days 511 (227-778) 373 (210-922) 602 (453-822) 529 (76-772) .48 .37 
Time to CMV reactivation, median (IQR), posttransplant days 30 (12-35) NA 34 (15-57) 18 (5-33) n/a .03 
CMV reactivation within 30 d posttransplant 12 (29) NA 6 (38) 6 (46) n/a .72 
Initial CMV DNAemia, median (IQR), IU/mL 106 (96-137) NA 102 (96-137) 106 (96-181) n/a .62 
Peak CMV DNAemia, median (IQR), IU/mL 377 (137-1800) NA 140 (137-192) 1,832 (1600-9189) n/a <.0001 
CMV DNAemia preceding therapy, median (IQR), IU/mL 873 (700-1500) NA n/a 873 (700-1500) n/a n/a 
Duration of CMV DNAemia, median (IQR), d 30 (22-40) NA 22 (5-32) 40 (30-60) n/a .0008 
CMV DNAemia lasting >7 d 24 (57) NA 11 (69) 13 (100) n/a .048 
Recurrent CMV DNAemia (ie, ≥2 episodes of viremia) 10 (26) NA 4 (25) 6 (60) n/a .11 
CMV disease 4 (9.5) 1 (6.3) 3 (23) .18 .29 
Underlying diagnosis       
 Leukemia 24 (57) 10 (77) 8 (50) 6 (46) .25 >.99 
 Lymphoma 6 (14) 1 (8) 1 (6) 4 (31) .22 .14 
 MDS/MPN 12 (29) 2 (15) 7 (44) 3 (23) .25 .43 
Conditioning regimen       
 Myeloablative§ 11 (26) 3 (23) 2 (13) 6 (46) .2 .1 
Stem cell source       
 Peripheral blood 41 (98) 13 (100) 16 (100) 12 (92) .62 .44 
 Bone marrow 1 (2) 1 (8)   
Type of donor       
 Unrelated 20 (48) 4 (31) 5 (31) 11 (85) .006 .008 
 HLA-matched related 22 (52) 9 (69) 11 (69) 2 (15)   
Malignancy status at time of transplant       
 Complete remission 26 (62) 9 (69) 9 (56) 8 (62) .92 >.99 
 Time to engraftment, median (IQR), d 10 (11-13) 11 (9-18) 11 (10-13) 12 (11-19) .49 .28 
 aGVHD (grade 2-4) 13 (31) 3 (23) 5 (31) 5 (38) .65 .71 
 Steroids (>0.5mg/kg), day 30 6 (14) 2 (15) 1 (6) 3 (23) .47 .29 
(D)onor/(R)ecipient CMV serostatus       
 D R+ 12 (29) 3 (23) 6 (38) 3 (23) .63 .45 
 D+ R+ 30 (71) 10 (77) 10 (62) 10 (77)   
CD34+ cells infused (1 × 106), median (IQR) 7.4 (5.8-9.4) 7.8 (6.7-12) 7.6 (6.5-10) 6.0 (3.5-7.3) .04 .045 
Charlson Comorbidity Score, median (IQR) 3 (2-5) 3 (2-4) 3 (2-5) 3 (2-7) .68 .49 
Lymphoid malignancy 11 (26) 5 (38) 1 (6) 5 (38) .06 .06 
Absolute lymphocyte count, day 30, cells/µL 800 (480-1380) 800 (350-1390) 950 (725-1623) 700 (250-1300) .35 .17 
Time to “day 30” sample collection, median (range), d 29 (27-31) 28 (25-31) 30 (28-32) 29 (27-31) .11 .15 
1-y bacterial or fungal invasive infections 8 (19) 2 (15) 1 (6) 5 (38) .13 .06 
100-d all-cause mortality 5 (12) 1 (8) 4 (31) .03 .03 
1-y all-cause mortality 9 (21) 2 (15) 2 (13) 5 (38) .25 .19 
3-y all-cause mortality 10 (24) 2 (15) 3 (19) 5 (38) .39 .41 
100-d NRM 3 (7) 1 (8) 2 (15) .28 .19 
1-y NRM 5 (12) 1 (8) 1 (6) 3 (23) .49 .29 
3-y NRM 5 (12) 1 (8) 1 (6) 3 (23) .49 .29 

Data are presented as absolute number (percentage), unless specified otherwise. Statistically significant P values (P < .05) are indicated in bold.

aGVHD, acute graft-versus-host disease; ATG, antithymocyte globulin; IQR, interquartile range; MDS/MPN, myelodysplastic syndrome/ myeloproliferative neoplasm.

*

P value for comparison between the 3 groups by using Kruskal-Wallis or Fisher’s exact test.

P value for comparison between SCs and NCs groups by using Mann-Whitney U or Fisher’s exact test.

Excluding 3 patients from the NCs group who never achieved viral clearance.

§

Other patients received reduced intensity conditioning. Missing data on 1 patient from SCs group.

Includes 4 mismatched unrelated donors and 16 matched unrelated donors. All unrelated donor recipients at our center undergo T-cell depletion with ATG during conditioning regimen. Typical dose of ATG at our center is 4 mg/kg total.

Median time from transplant to aGVHD was 108 d (IQR, 43-123).

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