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. 2020 Sep 28;4(19):4593–4604. doi: 10.1182/bloodadvances.2020002237

Table 1.

General and clinical characteristics of patients and controls

NDMM (n = 36) SMM (n = 11) MGUS (n = 24) Controls (n = 26)
Age, median (range), y 69 (38-90) 73 (50-85) 64 (42-89) 60 (35-84)
Sex, male, n (%) 20 (55) 5 (45) 7 (29) 12 (46)
ISS stage,* n (%)
 ISS1 11 (34) 3 (37.5) NA NA
 ISS2 10 (32) 3 (37.5) NA NA
 ISS3 11 (36) 2 (25) NA NA
Isotype, n (%)
 IgG 21 (60) NA NA NA
 IgA 8 (23) NA NA NA
 Light chain 6 (17) NA NA NA
 Oligosecretory 1 (3) NA NA NA
Cytogenetics, n (%) 33 (92) NA NA NA
 17p deletion 4 (12) NA NA NA
 −1p and/or +1q 13 (40) NA NA NA
FISH, n (%) 20 (55) NA NA NA
 t(4;14) 2 (11) NA NA NA
 t(14;16) 0 (0) NA NA NA
LDH, median (range), U/L 157 (89-407) NA NA NA
 Above normal, n (%) 5 (18) NA NA NA

FISH, fluorescence in situ hybridization; IgA, immunoglobulin A; IgG, immunoglobulin G; ISS, International Staging System; LDH, lactate dehydrogenase; NA, not available.

*

β2 microglobulin available for ISS grading in 32 out of 36 NDMM patients and 8 out of 11 SMM patients.

High-risk genetics by FISH, including del17p, t(4;14), and t(14;16), were tested in 20 out of 36 NDMM patients.

Available in 28 out of 36 NDMM patients.