Table 2.

Clinical characteristics of selected patients in the multiple myeloma subcohort with available periengraftment samples from days +9 to +16

CharacteristicMyeloma subcohort (n = 99)
Institution  
 MSKCC 65 (65.7) 
 Duke 34 (34.3) 
Mean age at auto-HCT, y (SD) 60.9 (8.6) 
Male sex 56 (56.6) 
Melphalan dose  
 200 mg/m2 74 (74.7) 
 140 mg/m2 23 (23.2) 
 180 mg 1 (1.0) 
 360 mg 1 (1.0) 
Status at transplant  
 Complete response/near complete response 15 (15.2) 
 Partial response 32 (32.3) 
 Very good partial response 48 (48.5) 
 Progressive disease or stable disease 3 (3.0) 
 Other 1 (1.0) 
Median follow-up of survivors, mo (IQR) 26.1 (16.4-36.6) 
International Staging System*  
 I 50 (50.5) 
 II 21 (21.2) 
 III 19 (19.2) 
Immunoglobulin  
 IgG κ 40 (40.4) 
 IgG λ 23 (23.2) 
 IgA κ 12 (12.1) 
 IgA λ 4 (4.0) 
κ free light chains 7 (7.1) 
λ free light chains 3 (3.0) 
Other 7 (7.1) 
Cytogenetic risk  
 Standard 52 (52.5) 
 High 31 (31.3) 
No. of previous lines of therapy  
 1 66 (66.7) 
 2 22 (22.2) 
 ≥3 11 (11.1) 
CharacteristicMyeloma subcohort (n = 99)
Institution  
 MSKCC 65 (65.7) 
 Duke 34 (34.3) 
Mean age at auto-HCT, y (SD) 60.9 (8.6) 
Male sex 56 (56.6) 
Melphalan dose  
 200 mg/m2 74 (74.7) 
 140 mg/m2 23 (23.2) 
 180 mg 1 (1.0) 
 360 mg 1 (1.0) 
Status at transplant  
 Complete response/near complete response 15 (15.2) 
 Partial response 32 (32.3) 
 Very good partial response 48 (48.5) 
 Progressive disease or stable disease 3 (3.0) 
 Other 1 (1.0) 
Median follow-up of survivors, mo (IQR) 26.1 (16.4-36.6) 
International Staging System*  
 I 50 (50.5) 
 II 21 (21.2) 
 III 19 (19.2) 
Immunoglobulin  
 IgG κ 40 (40.4) 
 IgG λ 23 (23.2) 
 IgA κ 12 (12.1) 
 IgA λ 4 (4.0) 
κ free light chains 7 (7.1) 
λ free light chains 3 (3.0) 
Other 7 (7.1) 
Cytogenetic risk  
 Standard 52 (52.5) 
 High 31 (31.3) 
No. of previous lines of therapy  
 1 66 (66.7) 
 2 22 (22.2) 
 ≥3 11 (11.1) 

All data represent no. (%), unless otherwise specified.

*

ISS data unavailable for 9 patients (9.1%).

Other incorporates biclonal, IgM κ, IgD λ, and nonsecretory subtypes. Unavailable for 3 patients (3.0%).

Cytogenetic risk unavailable for 16 patients (16.2%).

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