Table 6

Univariate regression model for overall mortality

VariableGroupHR95% CIPGlobal P
Marrow myeloblasts*  1.02 1.01-1.02 < .0001  
Hemoglobin*  0.95 0.90-1.01 .08  
Platelet count*  0.93 0.90-0.97 .0005  
Patient age*  1.07 1.02-1.12 .005  
Disease category MDS    
 tAML 1.57 1.34-1.86 < .0001  
IPSS cytogenetic risk Good   < .0001 
 Intermediate 1.16 0.93-1.45 .19  
 Poor 1.77 1.47-2.12 < .0001  
5-group cytogenetic risk Good   < .0001 
 Very good 1.15 0.57-2.32 .71  
 Intermediate 1.13 0.90-1.43 .28  
 Poor 1.29 1.01-1.63 .04  
 Very poor 3.08 2.40-3.94 < .0001  
 Data incomplete 1.88 1.50-2.36 < .0001  
Donor type Matched sibling   .01 
 Nonsibling relative 1.40 1.06-1.85 .02  
 URD matched 0.88 0.72-1.07 .19  
 URD mismatched 1.22 0.98-1.52 .07  
 URD unknown§ 0.89 0.57-1.40 .61  
Year of HCT*  0.97 0.96-0.99 < .0001  
Monosomal karyotype No    
 Yes 2.44 2.01-2.96 < .0001  
Secondary MDS No    
 Yes 1.33 1.11-1.58 .002  
Conditioning regimen BU + CY (± ATG)   < .0001 
 FLU + LD TBI 1.49 1.14-1.96 .004  
 BU + TBI (12 Gy) 2.21 1.65-2.95 < .0001  
 FLU + BU 1.46 1.01-2.10 .04  
 BU + CY + TBI (12 Gy) 1.86 1.30-2.67 .0007  
 131I + FLU + TBI (2 Gy) 1.86 1.15-3.00 .01  
 FLU + TREO 0.43 0.18-1.04 .06  
 CY + TBI (≥ 12 Gy) (± ATG) 1.66 1.35-2.03 < .0001  
 Other 1.69 1.11-2.57 .01  
FAB/WHO classification RA/RARS/RCMD   < .0001 
 RAEB 1.63 1.36-1.96 < .0001  
 RAEB-T 2.02 1.56-2.63 < .0001  
 tAML 2.37 1.86-3.02 < .0001  
Etiology de novo  < .0001  
 MPN 2.36 1.17-4.75 .03  
 Lymphoma 1.50 1.11-2.02 .008  
 Multiple myeloma 3.12 1.29-7.55 .01  
 Autoimmune disorders 1.76 1.08-2.85 .02  
 Organ transplant 2.64 0.85-8.22 .09  
 Accidental radiation exposure 11.4 2.83-46.1 .0006  
Treatment pre-HCT No   .01 
 IC 1.27 1.08-1.50 .004  
 IC + hypomethylation 0.51 0.07-3.63 .50  
 Hypomethylation 0.84 0.53-1.34 .47  
VariableGroupHR95% CIPGlobal P
Marrow myeloblasts*  1.02 1.01-1.02 < .0001  
Hemoglobin*  0.95 0.90-1.01 .08  
Platelet count*  0.93 0.90-0.97 .0005  
Patient age*  1.07 1.02-1.12 .005  
Disease category MDS    
 tAML 1.57 1.34-1.86 < .0001  
IPSS cytogenetic risk Good   < .0001 
 Intermediate 1.16 0.93-1.45 .19  
 Poor 1.77 1.47-2.12 < .0001  
5-group cytogenetic risk Good   < .0001 
 Very good 1.15 0.57-2.32 .71  
 Intermediate 1.13 0.90-1.43 .28  
 Poor 1.29 1.01-1.63 .04  
 Very poor 3.08 2.40-3.94 < .0001  
 Data incomplete 1.88 1.50-2.36 < .0001  
Donor type Matched sibling   .01 
 Nonsibling relative 1.40 1.06-1.85 .02  
 URD matched 0.88 0.72-1.07 .19  
 URD mismatched 1.22 0.98-1.52 .07  
 URD unknown§ 0.89 0.57-1.40 .61  
Year of HCT*  0.97 0.96-0.99 < .0001  
Monosomal karyotype No    
 Yes 2.44 2.01-2.96 < .0001  
Secondary MDS No    
 Yes 1.33 1.11-1.58 .002  
Conditioning regimen BU + CY (± ATG)   < .0001 
 FLU + LD TBI 1.49 1.14-1.96 .004  
 BU + TBI (12 Gy) 2.21 1.65-2.95 < .0001  
 FLU + BU 1.46 1.01-2.10 .04  
 BU + CY + TBI (12 Gy) 1.86 1.30-2.67 .0007  
 131I + FLU + TBI (2 Gy) 1.86 1.15-3.00 .01  
 FLU + TREO 0.43 0.18-1.04 .06  
 CY + TBI (≥ 12 Gy) (± ATG) 1.66 1.35-2.03 < .0001  
 Other 1.69 1.11-2.57 .01  
FAB/WHO classification RA/RARS/RCMD   < .0001 
 RAEB 1.63 1.36-1.96 < .0001  
 RAEB-T 2.02 1.56-2.63 < .0001  
 tAML 2.37 1.86-3.02 < .0001  
Etiology de novo  < .0001  
 MPN 2.36 1.17-4.75 .03  
 Lymphoma 1.50 1.11-2.02 .008  
 Multiple myeloma 3.12 1.29-7.55 .01  
 Autoimmune disorders 1.76 1.08-2.85 .02  
 Organ transplant 2.64 0.85-8.22 .09  
 Accidental radiation exposure 11.4 2.83-46.1 .0006  
Treatment pre-HCT No   .01 
 IC 1.27 1.08-1.50 .004  
 IC + hypomethylation 0.51 0.07-3.63 .50  
 Hypomethylation 0.84 0.53-1.34 .47  

CMV status and source of stem cells had no significant impact on outcome.

URD indicates unrelated donor; ATG, antithymocyte globulin; LD, low-dose TBI (2-4.5 Gy); TREO, treosulfan; MPN, myeloproliferative neoplasm; and IC, induction chemotherapy.

*

Modeled as continuous linear variables (as specified in Table 5);

Other regimens used (CY + TMI; FLU + TBI + CY; CY + BU) did not result in a significant difference.

Other antecedent conditions (aplastic anemia; constitutional marrow failure syndromes; solid tumors; other leukemias) had no significant impact.

§

Allele level typing was not performed.

Close Modal

or Create an Account

Close Modal
Close Modal