Table 7.

Six-month landmark analysis for OS

Immune variable*nHR (95% CI)P
ALC 92 0.20 (0.07-0.54) .003 
CD3+ T cells 93 0.34 (0.19-0.61) .001 
CD4+ T cells 93 0.30 (0.16-0.56) <.001 
CD4+CD45RA+ T cells 93 0.90 (0.59-1.39) .651 
CD8+ T cells 93 0.74 (0.45-1.21) .221 
NK cells 93 0.85 (0.31-2.34) .757 
B cells 93 0.80 (0.64-0.99) .054 
PHA 89 0.34 (0.17-0.68) .004 
Immune variable*nHR (95% CI)P
ALC 92 0.20 (0.07-0.54) .003 
CD3+ T cells 93 0.34 (0.19-0.61) .001 
CD4+ T cells 93 0.30 (0.16-0.56) <.001 
CD4+CD45RA+ T cells 93 0.90 (0.59-1.39) .651 
CD8+ T cells 93 0.74 (0.45-1.21) .221 
NK cells 93 0.85 (0.31-2.34) .757 
B cells 93 0.80 (0.64-0.99) .054 
PHA 89 0.34 (0.17-0.68) .004 

P values significant at the .01 level are indicated in bold.

*

In univariable analysis of patient, graft, and posttransplant variables, only recipient age was associated with OS, although not at the 0.01 significance level (HR, 1.78 [95% CI, 1.04-3.03] per decade, P = .025). Patient sex, diagnosis, CMV seropositivity, engrafting CB unit–recipient HLA-match, engrafting CB unit infused viable CD34+ and CD3+ cell doses, addition of haploidentical CD34+ cells, and day 100 aGVHD grade were not significant.

HR adjusted for age.

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