Table 4

Factors associated with poor T-cell reconstitution (CD4+ T cells <600 cells/mm3) at 2 years post-HCT

VariableOR (95% CI)P*aOR (95% CI)P*
Native American 6.0 (3.6-9.9) <.0001   
Omenn syndrome 0.5 (0.3-1.0) .05   
Ulcers 4.5 (2.4-8.5) <.0001 8.4 (3.0-23.4) <.0001 
No myeloablative conditioning 3.5 (2.3-5.4) <.0001 3.0 (2.0-4.5) <.0001 
Any alkylator therapy 0.4 (0.3-0.7) .001   
No myeloid chimerism (recipient) 7.4 (1.8-30.6) .005 6.3 (1.9-20.7) .002 
IVIG requirement 4.7 (1.5-15.0) .01   
CD4+ T cells at 1 y post-HCT 12.4 (2.4-65.0) .003   
VariableOR (95% CI)P*aOR (95% CI)P*
Native American 6.0 (3.6-9.9) <.0001   
Omenn syndrome 0.5 (0.3-1.0) .05   
Ulcers 4.5 (2.4-8.5) <.0001 8.4 (3.0-23.4) <.0001 
No myeloablative conditioning 3.5 (2.3-5.4) <.0001 3.0 (2.0-4.5) <.0001 
Any alkylator therapy 0.4 (0.3-0.7) .001   
No myeloid chimerism (recipient) 7.4 (1.8-30.6) .005 6.3 (1.9-20.7) .002 
IVIG requirement 4.7 (1.5-15.0) .01   
CD4+ T cells at 1 y post-HCT 12.4 (2.4-65.0) .003   

n = 76 patients (still alive after 2 y post-HCT). Only significant results in univariate analysis are shown. Patients were clustered using a group variable to take into account the practice variations between centers.

aOR, adjusted odds ratio.

*

P values are referring to univariate analysis (left column) and multivariate analysis (right column), respectively.

Variable not kept in the multivariate model because of colinearity with ulcers.

Category analyzing all conditioning regimens containing the following alkylating agents including both immunosuppressive and stem cell–toxic regimens: busulfan, treosulfan, thiothepa, melphalan, cyclophosphamide.

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