Table 1.

Characteristics and outcomes of patients with mWT1 stratified by single WT1 or mhWT1

VariablemhWT1P value
NoYes
(n = 20)(n = 13)
Age at diagnosis, y    
Median (min, max) 46.8 (18.4, 67.5) 42.7 (26.7, 71.8) .85 
Age at alloSCT, y    
Median (min, max) 48.0 (18.7, 68.0) 44.1 (27.5, 72.2) .8 
Sex    
Female 9 (45.0%) 3 (23.1%) .36 
Male 11 (55.0%) 10 (76.9%)  
Ethnicity    
Caucasian 17 (85.0%) 11 (84.6%) 
Other 3 (15.0%) 2 (15.4%)  
WT1 first detected    
Initial diagnosis 14 (70.0%) 7 (53.8%) .57 
Relapse 6 (30.0%) 6 (46.2%)  
Disease characteristics  
Disease  
AML 15 (75%) 10 (76.9%) .39 
MDS 1 (5%) 2 (15.4%)  
MPAL 1 (5%) 1 (7.7%)  
Others 3 (15%) 0 (0%)  
Hemoglobin ≥ 10 g/dL at diagnosis  
No 17 (85.0%) 11 (84.6%) 
Yes 2 (10.0%) 1 (7.7%)  
Missing 1 (5.0%) 1 (7.7%)  
Platelets ≥ 100 × 103/μL at diagnosis  
No 12 (60.0%) 10 (76.9%) .42 
Yes 7 (35.0%) 2 (15.4%)  
Missing 1 (5.0%) 1 (7.7%)  
Abnormal karyotype at diagnosis   
No 8 (40.0%) 8 (61.5%) .47 
Yes 11 (55.0%) 5 (38.5%)  
Missing 1 (5.0%) 0 (0%)  
Monosomy 7 at diagnosis    
No 18 (90.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
Missing 1 (5.0%) 0 (0%)  
Complex karyotype at diagnosis   
No 16 (80.0%) 13 (100%) .38 
Yes 3 (15.0%) 0 (0%)  
Missing 1 (5.0%) 0 (0%)  
Monosomal karyotype at diagnosis  
No 18 (90.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
Missing 1 (5.0%) 0 (0%)  
maxWT1 VAF    
Median [min, max] 34.5 [4.00, 84.0] 33.0 [12.0, 49.0] .66 
Isolated WT1 (no comutation)   
No 15 (75.0%) 13 (100%) .14 
Yes 5 (25.0%) 0 (0%)  
mWT1 in codons 301-303   
No 19 (95.0%) 7 (53.8%) .02 
Yes 1 (5.0%) 6 (46.2%)  
mWT1 in codons 312-314   
No 14 (70.0%) 5 (38.5%) .15 
Yes 6 (30.0%) 8 (61.5%)  
mWT1 in zinc-finger motif   
No 17 (85.0%) 11 (84.6%) 
Yes 3 (15.0%) 2 (15.4%)  
CR/CRi at alloSCT    
No 2 (10.0%) 3 (23.1%) .64 
Yes 17 (85.0%) 10 (76.9%)  
Missing 1 (5.0%) 0 (0%)  
DRI    
Low 3 (15%) 1 (7.7%) .83 
Intermediate 13 (65%) 9 (69.2%)  
High 3 (15%) 2 (15.4%)  
NA 1 (5%) 1 (7.7%)  
Comutations    
ASXL1    
No 17 (85.0%) 13 (100%) .40 
Yes 3 (15.0%) 0 (0%)  
BCOR    
No 19 (95.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
CEBPA    
No 17 (85.0%) 9 (69.2%) .52 
Yes 3 (15.0%) 4 (30.8%)  
CSF3R    
No 19 (95.0%) 12 (92.3%) 
Yes 1 (5.0%) 1 (7.7%)  
DNMT3A    
No 19 (95.0%) 10 (76.9%) .31 
Yes 1 (5.0%) 3 (23.1%)  
FLT3    
No 14 (70.0%) 4 (30.8%) .06 
Yes 6 (30.0%) 9 (69.2%)  
IDH1    
No 19 (95.0%) 12 (92.3%) 
Yes 1 (5.0%) 1 (7.7%)  
IDH2    
No 19 (95.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
GATA2    
No 19 (95.0%) 12 (92.3%) 
Yes 1 (5.0%) 1 (7.7%)  
JAK2    
No 19 (95.0%) 12 (92.3%) 
Yes 1 (5.0%) 1 (7.7%)  
KRAS    
No 19 (95.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
NPM1    
No 18 (90.0%) 11 (84.6%) 
Yes 2 (10.0%) 2 (15.4%)  
NRAS    
No 17 (85.0%) 12 (92.3%) .93 
Yes 3 (15.0%) 1 (7.7%)  
PHF6    
No 19 (95.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
PTPN11    
No 19 (95.0%) 11 (84.6%) .69 
Yes 1 (5.0%) 2 (15.4%)  
RUNX1    
No 18 (90.0%) 9 (69.2%) .29 
Yes 2 (10.0%) 4 (30.8%)  
SF3B1    
No 20 (100%) 11 (84.6%) .29 
Yes 0 (0%) 2 (15.4%)  
SRSF2    
No 19 (95.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
TET2    
No 18 (90.0%) 12 (92.3%) 
Yes 2 (10.0%) 1 (7.7%)  
TP53    
No 19 (95.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
ZRSR2    
No 19 (95.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
Transplantation characteristics and outcomes    
HCT-CI ≥ 3    
No 11 (55.0%) 9 (69.2%) .65 
Yes 9 (45.0%) 4 (30.8%)  
Conditioning intensity   
Myeloablative 12 (60.0%) 8 (61.5%) 
Reduced intensity 7 (35.0%) 5 (38.5%)  
Missing 1 (5.0%) 0 (0%)  
Conditioning    
Bu/Cy 4 (20.0%) 1 (7.7%) NA 
Bu/Flu 4 (20.0%) 3 (23.1%)  
Bu/Flu/ATG 1 (5.0%) 0 (0%)  
Cy/Flu/thiotepa/TLI 2 (10.0%) 0 (0%)  
Cy/TBI 2 (10.0%) 2 (15.4%)  
Flu/Mel 4 (20.0%) 4 (30.8%)  
Flu/TBI 2 (10.0%) 1 (7.7%)  
Bu/Cy/ATG 0 (0%) 1 (7.7%)  
Flu/BCNU/Mel 1 (5%) 1 (7.7%)  
Graft source    
Peripheral blood 18 (90.0%) 13 (100%) 
Bone marrow 1 (5.0%) 0 (0%)  
Missing 1 (5.0%) 0 (0%)  
Donor type    
MRD 5 (25.0%) 1 (7.7%) .36 
MUD 11 (55.0%) 9 (69.2%)  
MMUD 0 (0%) 1 (7.7%)  
Haploidentical 4 (20.0%) 2 (15.4%)  
Major/bidirectional ABO mismatch  
No 15 (75.0%) 10 (76.9%) 
Yes 4 (20.0%) 3 (23.1%)  
Missing 1 (5.0%) 0 (0%)  
GVHD prophylaxis   
CD34 selection 1 (5.0%) 0 (0%) .16 
Tacrolimus + methotrexate (± ATG) 13 (65%) 9 (69.3%)  
Cyclosporine + methotrexate 2 (10.0%) 1 (7.7%)  
Tacrolimus + mycophenolate 3 (15.0%) 0 (0%)  
PT-Cy based 0 (0%) 3 (23.1%)  
None 1 (5.0%) 0 (0%)  
Grade 2-4 acute GVHD   
No 17 (85.0%) 10 (76.9%) .9 
Yes 3 (15.0%) 3 (23.1%)  
Grade 3-4 acute GVHD   
No 13 (65.0%) 12 (92.3%) .17 
Yes 7 (35.0%) 1 (7.7%)  
Moderate/severe chronic GVHD   
No 18 (90.0%) 11 (84.6%) 
Yes 2 (10.0%) 2 (15.4%)  
VariablemhWT1P value
NoYes
(n = 20)(n = 13)
Age at diagnosis, y    
Median (min, max) 46.8 (18.4, 67.5) 42.7 (26.7, 71.8) .85 
Age at alloSCT, y    
Median (min, max) 48.0 (18.7, 68.0) 44.1 (27.5, 72.2) .8 
Sex    
Female 9 (45.0%) 3 (23.1%) .36 
Male 11 (55.0%) 10 (76.9%)  
Ethnicity    
Caucasian 17 (85.0%) 11 (84.6%) 
Other 3 (15.0%) 2 (15.4%)  
WT1 first detected    
Initial diagnosis 14 (70.0%) 7 (53.8%) .57 
Relapse 6 (30.0%) 6 (46.2%)  
Disease characteristics  
Disease  
AML 15 (75%) 10 (76.9%) .39 
MDS 1 (5%) 2 (15.4%)  
MPAL 1 (5%) 1 (7.7%)  
Others 3 (15%) 0 (0%)  
Hemoglobin ≥ 10 g/dL at diagnosis  
No 17 (85.0%) 11 (84.6%) 
Yes 2 (10.0%) 1 (7.7%)  
Missing 1 (5.0%) 1 (7.7%)  
Platelets ≥ 100 × 103/μL at diagnosis  
No 12 (60.0%) 10 (76.9%) .42 
Yes 7 (35.0%) 2 (15.4%)  
Missing 1 (5.0%) 1 (7.7%)  
Abnormal karyotype at diagnosis   
No 8 (40.0%) 8 (61.5%) .47 
Yes 11 (55.0%) 5 (38.5%)  
Missing 1 (5.0%) 0 (0%)  
Monosomy 7 at diagnosis    
No 18 (90.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
Missing 1 (5.0%) 0 (0%)  
Complex karyotype at diagnosis   
No 16 (80.0%) 13 (100%) .38 
Yes 3 (15.0%) 0 (0%)  
Missing 1 (5.0%) 0 (0%)  
Monosomal karyotype at diagnosis  
No 18 (90.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
Missing 1 (5.0%) 0 (0%)  
maxWT1 VAF    
Median [min, max] 34.5 [4.00, 84.0] 33.0 [12.0, 49.0] .66 
Isolated WT1 (no comutation)   
No 15 (75.0%) 13 (100%) .14 
Yes 5 (25.0%) 0 (0%)  
mWT1 in codons 301-303   
No 19 (95.0%) 7 (53.8%) .02 
Yes 1 (5.0%) 6 (46.2%)  
mWT1 in codons 312-314   
No 14 (70.0%) 5 (38.5%) .15 
Yes 6 (30.0%) 8 (61.5%)  
mWT1 in zinc-finger motif   
No 17 (85.0%) 11 (84.6%) 
Yes 3 (15.0%) 2 (15.4%)  
CR/CRi at alloSCT    
No 2 (10.0%) 3 (23.1%) .64 
Yes 17 (85.0%) 10 (76.9%)  
Missing 1 (5.0%) 0 (0%)  
DRI    
Low 3 (15%) 1 (7.7%) .83 
Intermediate 13 (65%) 9 (69.2%)  
High 3 (15%) 2 (15.4%)  
NA 1 (5%) 1 (7.7%)  
Comutations    
ASXL1    
No 17 (85.0%) 13 (100%) .40 
Yes 3 (15.0%) 0 (0%)  
BCOR    
No 19 (95.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
CEBPA    
No 17 (85.0%) 9 (69.2%) .52 
Yes 3 (15.0%) 4 (30.8%)  
CSF3R    
No 19 (95.0%) 12 (92.3%) 
Yes 1 (5.0%) 1 (7.7%)  
DNMT3A    
No 19 (95.0%) 10 (76.9%) .31 
Yes 1 (5.0%) 3 (23.1%)  
FLT3    
No 14 (70.0%) 4 (30.8%) .06 
Yes 6 (30.0%) 9 (69.2%)  
IDH1    
No 19 (95.0%) 12 (92.3%) 
Yes 1 (5.0%) 1 (7.7%)  
IDH2    
No 19 (95.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
GATA2    
No 19 (95.0%) 12 (92.3%) 
Yes 1 (5.0%) 1 (7.7%)  
JAK2    
No 19 (95.0%) 12 (92.3%) 
Yes 1 (5.0%) 1 (7.7%)  
KRAS    
No 19 (95.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
NPM1    
No 18 (90.0%) 11 (84.6%) 
Yes 2 (10.0%) 2 (15.4%)  
NRAS    
No 17 (85.0%) 12 (92.3%) .93 
Yes 3 (15.0%) 1 (7.7%)  
PHF6    
No 19 (95.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
PTPN11    
No 19 (95.0%) 11 (84.6%) .69 
Yes 1 (5.0%) 2 (15.4%)  
RUNX1    
No 18 (90.0%) 9 (69.2%) .29 
Yes 2 (10.0%) 4 (30.8%)  
SF3B1    
No 20 (100%) 11 (84.6%) .29 
Yes 0 (0%) 2 (15.4%)  
SRSF2    
No 19 (95.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
TET2    
No 18 (90.0%) 12 (92.3%) 
Yes 2 (10.0%) 1 (7.7%)  
TP53    
No 19 (95.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
ZRSR2    
No 19 (95.0%) 13 (100%) 
Yes 1 (5.0%) 0 (0%)  
Transplantation characteristics and outcomes    
HCT-CI ≥ 3    
No 11 (55.0%) 9 (69.2%) .65 
Yes 9 (45.0%) 4 (30.8%)  
Conditioning intensity   
Myeloablative 12 (60.0%) 8 (61.5%) 
Reduced intensity 7 (35.0%) 5 (38.5%)  
Missing 1 (5.0%) 0 (0%)  
Conditioning    
Bu/Cy 4 (20.0%) 1 (7.7%) NA 
Bu/Flu 4 (20.0%) 3 (23.1%)  
Bu/Flu/ATG 1 (5.0%) 0 (0%)  
Cy/Flu/thiotepa/TLI 2 (10.0%) 0 (0%)  
Cy/TBI 2 (10.0%) 2 (15.4%)  
Flu/Mel 4 (20.0%) 4 (30.8%)  
Flu/TBI 2 (10.0%) 1 (7.7%)  
Bu/Cy/ATG 0 (0%) 1 (7.7%)  
Flu/BCNU/Mel 1 (5%) 1 (7.7%)  
Graft source    
Peripheral blood 18 (90.0%) 13 (100%) 
Bone marrow 1 (5.0%) 0 (0%)  
Missing 1 (5.0%) 0 (0%)  
Donor type    
MRD 5 (25.0%) 1 (7.7%) .36 
MUD 11 (55.0%) 9 (69.2%)  
MMUD 0 (0%) 1 (7.7%)  
Haploidentical 4 (20.0%) 2 (15.4%)  
Major/bidirectional ABO mismatch  
No 15 (75.0%) 10 (76.9%) 
Yes 4 (20.0%) 3 (23.1%)  
Missing 1 (5.0%) 0 (0%)  
GVHD prophylaxis   
CD34 selection 1 (5.0%) 0 (0%) .16 
Tacrolimus + methotrexate (± ATG) 13 (65%) 9 (69.3%)  
Cyclosporine + methotrexate 2 (10.0%) 1 (7.7%)  
Tacrolimus + mycophenolate 3 (15.0%) 0 (0%)  
PT-Cy based 0 (0%) 3 (23.1%)  
None 1 (5.0%) 0 (0%)  
Grade 2-4 acute GVHD   
No 17 (85.0%) 10 (76.9%) .9 
Yes 3 (15.0%) 3 (23.1%)  
Grade 3-4 acute GVHD   
No 13 (65.0%) 12 (92.3%) .17 
Yes 7 (35.0%) 1 (7.7%)  
Moderate/severe chronic GVHD   
No 18 (90.0%) 11 (84.6%) 
Yes 2 (10.0%) 2 (15.4%)  

ATG, anti-thymocyte globulin; BCNU, carmustine; Bu, busulfan; CRi, complete remission with incomplete count recovery; Cy, cyclophosphamide; Flu, fludarabine; GVHD, graft-versus-host disease; HCT-CI, hematopoietic stem cell transplant comorbidity index; max, maximum; Mel, melphalan; min, minimum; MRD, matched related donor; MMUD, mismatched unrelated donor; MUD, matched unrelated donor; PT, posttransplant; TBI, total body irradiation; TLI, total lymphoid irradiation; VAF, variant allele frequency.

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