Table 5.

Definitions for MRD response categories and MRD relapse

Response categoryAbbreviationDefining criteria
CR with negative MRD CRMRD− 1. Complete morphologic remission and
2. MRD in all MRD technologies that were used:
  • a. FC-MRD in BM (if MFC-MRD was used).

  • b. qPCR-MRD in BM (or in PB after cycle 2 for NPM1- and CBF-MRD) (if qPCR-MRD was used).

  • c. NGS-MRD in BM (if NGS-MRD was used).

 
CR with positive MRD CRMRD1. Complete morphologic remission, and
2. MFC-MRD+in PB and/or BM, or
3. NGS-MRD+ in PB and/or BM, or
4. qPCR-MRD+ in PB and/or BM. 
CR with molecular MRD detection at low level CR-MRD-LL 1. Morphologic CR, and
2. Molecular MRD detectable at low level in PB and/or BM (ie, qPCR for NPM1
<2% or NGS-MRD <0.1%, but above the detection limit of the assay). 
MRD relapse  1. Conversion of MRD negativity to MRD positivity independent of the MRD
technique, or
2. increase in MRD copy numbers ≥1 log10 between any 2 positive samples in
patients with CR-MRD-LL who are monitored by qPCR.
3. The result of (1) or (2) should be rapidly confirmed in a second consecutive
sample, preferably from the BM. 
Response categoryAbbreviationDefining criteria
CR with negative MRD CRMRD− 1. Complete morphologic remission and
2. MRD in all MRD technologies that were used:
  • a. FC-MRD in BM (if MFC-MRD was used).

  • b. qPCR-MRD in BM (or in PB after cycle 2 for NPM1- and CBF-MRD) (if qPCR-MRD was used).

  • c. NGS-MRD in BM (if NGS-MRD was used).

 
CR with positive MRD CRMRD1. Complete morphologic remission, and
2. MFC-MRD+in PB and/or BM, or
3. NGS-MRD+ in PB and/or BM, or
4. qPCR-MRD+ in PB and/or BM. 
CR with molecular MRD detection at low level CR-MRD-LL 1. Morphologic CR, and
2. Molecular MRD detectable at low level in PB and/or BM (ie, qPCR for NPM1
<2% or NGS-MRD <0.1%, but above the detection limit of the assay). 
MRD relapse  1. Conversion of MRD negativity to MRD positivity independent of the MRD
technique, or
2. increase in MRD copy numbers ≥1 log10 between any 2 positive samples in
patients with CR-MRD-LL who are monitored by qPCR.
3. The result of (1) or (2) should be rapidly confirmed in a second consecutive
sample, preferably from the BM. 

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