Table 6.

Multivariate analysis for specific toxicities (grades 3-5) and NRM



Infection

Hepatic

1-year NRM
Risk factor
OR (95% CI)
P
OR (95% CI)
P
HR (95% CI)
P
Type of regimen       
   Nonablative vs ablative   0.2 (0.1-0.4)   < 10-4  0.3 (0.1-0.6)   .002   0.4 (0.2-1.0)   .06  
Comorbidity score   NS    NS    .002  
   0       Reference   
   1,2       3.3 (1.6-7.1)   
   3 or more       7.9 (2.0-31)   
CMV risk*       
   High vs low/intermediate   3.4 (1.4-8.1)   .004    NS    NS  
Diagnosis group   .04    NS    NS  
   AML, MDS   Reference       
   MM   0.3 (0.1-0.9)       
   NHL, HD, Waldenstrom   0.5 (0.2-1.6)       
   CLL, CML, ALL   1.5 (0.4-5.5)       
Hematopoietic cell source       
   Marrow vs G-PBMC
 

 
NS
 
3.1 (1.1-8.8)
 
.03
 
2.9 (1.3-6.9)
 
.02
 


Infection

Hepatic

1-year NRM
Risk factor
OR (95% CI)
P
OR (95% CI)
P
HR (95% CI)
P
Type of regimen       
   Nonablative vs ablative   0.2 (0.1-0.4)   < 10-4  0.3 (0.1-0.6)   .002   0.4 (0.2-1.0)   .06  
Comorbidity score   NS    NS    .002  
   0       Reference   
   1,2       3.3 (1.6-7.1)   
   3 or more       7.9 (2.0-31)   
CMV risk*       
   High vs low/intermediate   3.4 (1.4-8.1)   .004    NS    NS  
Diagnosis group   .04    NS    NS  
   AML, MDS   Reference       
   MM   0.3 (0.1-0.9)       
   NHL, HD, Waldenstrom   0.5 (0.2-1.6)       
   CLL, CML, ALL   1.5 (0.4-5.5)       
Hematopoietic cell source       
   Marrow vs G-PBMC
 

 
NS
 
3.1 (1.1-8.8)
 
.03
 
2.9 (1.3-6.9)
 
.02
 

Other factors considered, but not found to be significant, were age, previous HCT, time from diagnosis to transplantation, disease risk, and donor sex. NRM indicates nonrelapse mortality; OR, odds ratio; HR, hazard ratio; CI, confidence interval; NS, not significant; CMV, cytomegalovirus; AML, acute myeloid leukemia; MDS, myelodysplastic syndrome; MM, multiple myeloma; NHL, non-Hodgkin lymphoma; HD, Hodgkin disease; CLL, chronic lymphocytic leukemia; CML, chronic myelogenous leukemia; ALL, acute lymphocytic leukemia; G-PBMC, granulocyte colony-stimulating factor-mobilized peripheral blood mononuclear cells.

*

High-risk CMV indicates patient CMV+

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