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. 2020 Jul 20;4(14):3224–3233. doi: 10.1182/bloodadvances.2020001927

Table 6.

Differences between studies

Characteristic CIBMTR Current 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.