Table 2

Summary of disease and stage risk groups from original DRI

DiseaseDisease risk
 AML favorable cytogenetics Low 
 CLL 
 CML 
 Indolent B-cell NHL 
 ALL Intermediate 
 AML intermediate cytogenetics 
 MDS intermediate cytogenetics 
 Myeloproliferative neoplasms 
 Multiple myeloma 
 HL 
 DLBCL/transformed indolent B-cell NHL 
 Mantle cell lymphoma 
 Low-risk T-cell lymphoma 
 AML adverse cytogenetics High 
 MDS adverse cytogenetics 
 High-risk T-cell lymphoma 
Stage Stage risk 
 Any CR Low 
 PR (including improved but <CR MDS/MPN) 
 Untreated 
 Chronic phase CML 
 Induction failure High 
 Active relapse 
 Accelerated or blast phase CML 
Overall assignment   
Disease risk Stage risk DRI assignment 
Low Low Low 
Low High Intermediate 
Intermediate Low 
Intermediate High High 
High Low 
High High Very high 
DiseaseDisease risk
 AML favorable cytogenetics Low 
 CLL 
 CML 
 Indolent B-cell NHL 
 ALL Intermediate 
 AML intermediate cytogenetics 
 MDS intermediate cytogenetics 
 Myeloproliferative neoplasms 
 Multiple myeloma 
 HL 
 DLBCL/transformed indolent B-cell NHL 
 Mantle cell lymphoma 
 Low-risk T-cell lymphoma 
 AML adverse cytogenetics High 
 MDS adverse cytogenetics 
 High-risk T-cell lymphoma 
Stage Stage risk 
 Any CR Low 
 PR (including improved but <CR MDS/MPN) 
 Untreated 
 Chronic phase CML 
 Induction failure High 
 Active relapse 
 Accelerated or blast phase CML 
Overall assignment   
Disease risk Stage risk DRI assignment 
Low Low Low 
Low High Intermediate 
Intermediate Low 
Intermediate High High 
High Low 
High High Very high 

For this study, patients in first and subsequent PR were grouped and assigned to low risk regardless of conditioning intensity. BL was excluded from the cohort for this validation because it was not included in the original DRI.

DLBCL, diffuse large B-cell lymphoma; MPN, myeloproliferative neoplasms.

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