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. 2021 May 5;9(3):771–776. doi: 10.1002/iid3.431

Table 1.

Univariate analysis for clinically significant CMV infection risk factors during letermovir prophylaxis

Odds ratio 95% CI p value
Patients characteristics and HCT variables
Cause of letermovir prophylaxis, D‐R+ versus GvHD 1.3 0.2, 7.5 0.78
Age 1.0 0.9, 1.1 0.63
Gender, female versus male 1.5 0.2, 9.6 0.69
Underlying hematologic malignancy, myeloid versus lymphoid 0.9 0.1, 5.8 0.88
Malignancy remission before HCT, Yes versus No 2.1 0.3, 17 0.47
Conditioning regimen, nonmyeloablative versus myeloablative NA NA NA
HLA‐matched related versus HLA‐matched unrelated versus haploidentical 3.2 0.7, 14.9 0.14
Stem cells origin, bone marrow versus Peripheral blood stem cells 1.4 0.1, 18.6 0.79
Time to engraftment 1.0 0.9, 1.2 0.78
Acute GvHD grade ≥2 at baseline, Yes versus No 1.3 0.2, 7.5 0.78
Acute GvHD grade ≥2 post baseline, Yes versus No 6.4 0.8, 51.8 0.08
Refractory GvHD at baseline, Yes versus No NA NA NA
GIT GvHD at baseline, Yes versus No 2.1 0.3, 12.9 0.42
GIT GvHD post baseline, Yes versus No 13.5 1.1, 166 0.04
CMV serological status, D+R+ versus D−R+ 1.4 0.2, 9.6 0.69
EBV serological status 1.4 0.3, 6.1 0.62
Toxoplasmosis serological status 1.2 0.6, 2.5 0.57
CMV PCR variables until end of prophylaxis
Positive PCR at baseline (21–149 IU/ml) 7.1 1.0, 49.5 0.05
Total number of positive PCR (21–149 IU/ml) 1.8 1.1, 3.1 0.03
2 consecutive positive PCR (21–149 IU/ml) in the first 2 weeks 3.6 0.4, 31.2 0.25
3 consecutive positive PCR (21–149 IU/ml) 15.0 1.3, 174.4 0.03
More than 3 positive PCR (21–149 IU/ml) 34.0 2.4, 474 0.009
More than 3 consecutive positive PCR (21–149 IU/ml) 12.7 1.3, 128.8 0.03
At least 1 positive PCR between 100 and 149 IU/ml 13.5 1.1, 169 0.04

Abbreviations: +, positive; −, negative; D, donor; GvHD, GIT, gastro‐intestinal tract; GvHD, graft versus host disease; HCT, hematopoietic cell transplant; R, recipient.