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Table 1 Flow-MRD response assessment after treatment of multiple myeloma

From: Longitudinal minimal residual disease assessment in multiple myeloma patients in complete remission – results from the NMSG flow-MRD substudy within the EMN02/HO95 MM trial

 

Comment

Patients

Pts. with clinical progression (*1)

(A)

Patients registered/included into the study

Patients included into the study (Inclusion period: 01-03-2012 - 31-03-2014)

136

   

79

Patients with only diagnostic BM sample received (until 31-10-2018)

 

83

   

Patients with BM samples for Flow-MRD analysis received (until 31-08-2018)

 

53

  

29

(B)

1st flow RA (Flow-MRD analysis FU1)

Patients with BM samples received for 1st Flow-RA

 

53

   

Excluded patients not reaching RS of CR at 1st response assessment

  

31

 

13

Excluded patients (OFF-protocol)

  

1

 

1

Included patients with RS of CR/SCR at 1st response assessment

  

21

 

14

Included with adequate BM sample

   

15

 

Excluded with inadequate BM sample

   

6

 

(C)

Longitudinal flow-MRD analysis (FU1-FUX)

Patients with BM samples received for longitudinal analysis

 

53

   

Best reached RS during the patients course: <VGPR

   

2

1

Best reached RS during the patients course: VGPR

   

11

10

Best reached RS during the patients course: CR

   

12

5

Best reached RS during the patients course: sCR

   

28

13

Excluded patients (Off-protocol)

  

2

  

Excluded patients not reaching CR over the entire patients course

  

13

  

Excluded with inadequate BM samples (until progression)

  

4

  

Included patients with reached RS CR/SCR over the patients course

  

34

  

Included with ≥ 3 Flow-MRD samples analysed (incl. FU1)

   

20

7

Excluded with ≤ 2 Flow-MRD samples analysed (incl. FU1)

   

14

7

  1. Abbreviations: PR Partial response, VGPR Very good PR, CR Complete response, SCR Stringent CR, Flow-MRD MRD assessment using MFC, RA Response assessment, RS Clinical response category, FU Follow up (FU1 = 1st RA; FUX = subsequent follow ups), Pts Patients. Grey Boxes indicate patients included into the final analysis. (*1): at censoring date