Table 6.

Differences between studies

CharacteristicCIBMTRCurrent study
Centers Multiple Single 
Donor types Unrelated Related and unrelated 
HLA-A, -B, -C, -DRBI, and -DQB1 mismatching included No Yes 
No. of recipients, candidate SNP study Up to 2887 Up to 2560 for discovery 
No. of recipients, genome-wide study 1970 for discovery Up to 2560 for discovery 
Recipient diseases AML, ALL, MDS Any hematologic malignancy 
End points OS, PFS, NRM, RM NRM, RM 
End point adjudication Yes No 
No. of individual candidate variants 47 122 
Candidate SNP genetic models Allelic Allelic, dominant, recessive 
Adjustment for clinical covariates Yes No 
Truncation of follow-up 1 y None 
Tested recipient SNP allele mismatching Yes No 
GWAS scope Exomes Whole genome 
Statistical replication or validation Metaanalysis 3:2 discovery/replication split 
Gene-level analysis Yes No 
CharacteristicCIBMTRCurrent study
Centers Multiple Single 
Donor types Unrelated Related and unrelated 
HLA-A, -B, -C, -DRBI, and -DQB1 mismatching included No Yes 
No. of recipients, candidate SNP study Up to 2887 Up to 2560 for discovery 
No. of recipients, genome-wide study 1970 for discovery Up to 2560 for discovery 
Recipient diseases AML, ALL, MDS Any hematologic malignancy 
End points OS, PFS, NRM, RM NRM, RM 
End point adjudication Yes No 
No. of individual candidate variants 47 122 
Candidate SNP genetic models Allelic Allelic, dominant, recessive 
Adjustment for clinical covariates Yes No 
Truncation of follow-up 1 y None 
Tested recipient SNP allele mismatching Yes No 
GWAS scope Exomes Whole genome 
Statistical replication or validation Metaanalysis 3:2 discovery/replication split 
Gene-level analysis Yes No 

ALL indicates acute lymphoid leukemia; AML, acute myeloid leukemia; MDS, myelodysplastic syndrome.

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