Table 3.
Characteristic | Effect Ratio (95% CI) | P Value |
---|---|---|
Sample characteristics | ||
Upper-gut GVHD† | 1.04 (.80 to 1.33) | .78 |
Mid-gut GVHD† | 1.98 (1.20 to 3.29) | .008 |
Patient pretransplantation characteristics | ||
CMV seropositive pretransplantation | 1.32 (1.02 to 1.72) | .04 |
Donor CMV seropositive | 1.17 (.92 to 1.50) | .21 |
Unrelated donor | 1.35 (1.02 to 1.78) | .04 |
Mismatched donor | 1.09 (.76 to 1.57) | .63 |
Age (per decade) | 1.00 (.98 to 1.03) | .75 |
Female | .94 (.72 to 1.23) | .66 |
Female to male D/R | .86 (.62 to 1.20) | .37 |
PBSC | .93 (.56 to 1.56) | .79 |
TBI (>1200 cGy) | 1.14 (.88 to 1.47) | .33 |
GVHD indicates graft-versus-host disease; CMV, cytomegalovirus; PBSC, peripheral blood stem cells; TBI, total body irradiation; D/R, donor/recipient.
Multivariate analysis of soluble Tim-3 plasma levels in 303 samples collected from 127 patients before initiation of treatment for acute GVHD. Data were analyzed after log transformation of Tim-3 levels. The “effect ratio” is the antilog of the estimated difference in means on the log scale, and represents a multiplicative effect of covariates on Tim-3 levels. Models were also adjusted for time since HCT (linear, quadratic, and cubic terms).
Defined as any sample within 15 days of onset of treatment for GVHD and compared with grade 0 to 1 acute GVHD.