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. 2014 Oct 16;124(26):3996–4003. doi: 10.1182/blood-2014-09-599969

Table 2.

Level of HLA-C expression influences acute GVHD, nonrelapse mortality, and overall mortality, but not relapse

Nonshared HLA-C allotype* Acute GVHD (N = 453/1861) Nonrelapse mortality (N = 709/1727) Overall mortality (N = 1246/1975) Relapse (N = 501/1727)
OR (95% CI) P HR (95% CI) P HR (95% CI) P HR (95% CI) P
Patient’s mismatch 1.34 (1.10-1.62) .003 1.22 (1.06-1.39) .005 1.15 (1.03-1.27) .009 1.03 (0.86-1.22) .76
Donor’s mismatch 1.07 (0.88-1.30) .49 1.15 (1.01-1.31) .04 1.14 (1.03-1.26) .01 0.97 (0.82-1.16) .74
Sum of mismatched allotypes 1.16 (1.03-1.32) .02 1.15 (1.06-1.25) .002 1.12 (1.05-1.19) .001 1.00 (0.89-1.12) .96

The level of expression of the patient’s mismatch, the donor’s mismatch, and the sum of these mismatched allotypes were each modeled as a continuous linear variable. ORs and HRs are presented as an increase in risk of failure associated with each increase in expression of 100 fluorescence intensity units.

*

For the shared (matched) allotype, the OR for acute GVHD was 0.90 (95% CI, 0.71-1.13; P = .36), the HR for nonrelapse mortality was 0.85 (95% CI, 0.72-1.00; P = .05), the HR for overall mortality was 0.94 (95% CI, 0.84-1.07; P = .34), and the HR for relapse was 1.10 (95% CI, 0.90-1.34; P = .34).

Numbers denote the number of patients with failure for each of the 4 end points of all patients with clinical data for the given end point.