Table 1.

Studies on minimal residual disease (MRD) kinetics after allogeneic stem cell transplantation (alloSCT) for chronic lymphocytic leukemia (CLL) using quantitative MRD assays.

Ritgen et al21 Farina et al18 Moreno et al23*
* and C Moreno, personal communication, May 19, 2009 
a Fludarabine-cyclophosphamide; additional anti-thymocyte globulin (ATG) in unrelated donor transplants 
b Fludarabine-cyclophosphamide-thiotepa; cyclophosphamide-thiotepa-antithymocyte globulin in unrelated donor transplants 
c Cyclophosphamide, total body irradiation 12 Gy; or fludarabine, melphalan; or fludarabine, total body irradiation 2 Gy 
d MRD prior to CSA withdrawal or onset of chronic graft-versus-host disease (GVHD) 
e MRD only after CSA withdrawal, donor lymphocyte infusions (DLI), or onset of chronic GVHD 
f Mixed: not consistently negative, but without significant increase over time 
g Two patients had MRD recurrence concurrent with clinical relapse 33 and 62 months post alloSCT 
h Including all patients with a “mixed” pattern 
i Update March 31, 2009 
28 29 20 
Conditioning regimen FCy+/-ATGa FCyTT/CyTT-ATGb Cy/TBI, FMel, F/TBI2c 
MRD quantification assay RQ-PCR/MRD-Flow Nested PCR/RQ-PCR RQ-PCR/MRD-Flow 
MRD pattern 
    Permanent negativity 22 of 28 (79%) 9 of 29 (31%) 13 of 20 (65%) 
        Immediate negativityd 4 of 28 (14%) 5 of 29 (17%) 3 of 20 (15%) 
        Delayed negativitye 18 of 28 (64%) 4 of 29 (14%) 10 of 20 (50%) 
    Mixed patternf 7 of 29 (24%) 1 of 20 (5%) 
    Always positive 6 of 28 (21%) 13 of 29 (45%) 6 of 20 (30%) 
Relapse by MRD pattern 
    Permanent negativity 1 (4%) n.a. 
    Mixed pattern n.a. 1 (14%) n.a. 
    Always positive 5 (83%) 8 (62%) n.a. 
Clinical relapse in patients MRD 
    12 months post SCTg 1 of 19 (5%) 0 of 15h 1 of 9 (11%)e 
Follow-up of MRD patients (mo) 72 (41–101)i 40 (12–85) (6–204) 
Ritgen et al21 Farina et al18 Moreno et al23*
* and C Moreno, personal communication, May 19, 2009 
a Fludarabine-cyclophosphamide; additional anti-thymocyte globulin (ATG) in unrelated donor transplants 
b Fludarabine-cyclophosphamide-thiotepa; cyclophosphamide-thiotepa-antithymocyte globulin in unrelated donor transplants 
c Cyclophosphamide, total body irradiation 12 Gy; or fludarabine, melphalan; or fludarabine, total body irradiation 2 Gy 
d MRD prior to CSA withdrawal or onset of chronic graft-versus-host disease (GVHD) 
e MRD only after CSA withdrawal, donor lymphocyte infusions (DLI), or onset of chronic GVHD 
f Mixed: not consistently negative, but without significant increase over time 
g Two patients had MRD recurrence concurrent with clinical relapse 33 and 62 months post alloSCT 
h Including all patients with a “mixed” pattern 
i Update March 31, 2009 
28 29 20 
Conditioning regimen FCy+/-ATGa FCyTT/CyTT-ATGb Cy/TBI, FMel, F/TBI2c 
MRD quantification assay RQ-PCR/MRD-Flow Nested PCR/RQ-PCR RQ-PCR/MRD-Flow 
MRD pattern 
    Permanent negativity 22 of 28 (79%) 9 of 29 (31%) 13 of 20 (65%) 
        Immediate negativityd 4 of 28 (14%) 5 of 29 (17%) 3 of 20 (15%) 
        Delayed negativitye 18 of 28 (64%) 4 of 29 (14%) 10 of 20 (50%) 
    Mixed patternf 7 of 29 (24%) 1 of 20 (5%) 
    Always positive 6 of 28 (21%) 13 of 29 (45%) 6 of 20 (30%) 
Relapse by MRD pattern 
    Permanent negativity 1 (4%) n.a. 
    Mixed pattern n.a. 1 (14%) n.a. 
    Always positive 5 (83%) 8 (62%) n.a. 
Clinical relapse in patients MRD 
    12 months post SCTg 1 of 19 (5%) 0 of 15h 1 of 9 (11%)e 
Follow-up of MRD patients (mo) 72 (41–101)i 40 (12–85) (6–204) 

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