Table 4

Mechanism of diagnosis and incidence of SMM diagnosis in optimally followed patients with high-risk MGUS

VariableM spike ≥ 1.5 g/dL and/or non-IgG spike (n = 52; 65%)M spike < 1.5 g/dL and IgG spike (n = 27; 34%)P
SMM diagnosis preceding symptomatic MM, n (%) 20 (38) 4 (15) .04* 
Mechanism of MM diagnosis, n (%)    
    Complications 21 (40) 14 (52) .5 
    Symptoms 14 (27) 6 (22) .8 
    Follow-up 11 (21) 2 (7) .1 
    Incidental 4 (8) 5 (19) .3 
    Not available 2 (4) NA 
VariableM spike ≥ 1.5 g/dL and/or non-IgG spike (n = 52; 65%)M spike < 1.5 g/dL and IgG spike (n = 27; 34%)P
SMM diagnosis preceding symptomatic MM, n (%) 20 (38) 4 (15) .04* 
Mechanism of MM diagnosis, n (%)    
    Complications 21 (40) 14 (52) .5 
    Symptoms 14 (27) 6 (22) .8 
    Follow-up 11 (21) 2 (7) .1 
    Incidental 4 (8) 5 (19) .3 
    Not available 2 (4) NA 

Patients with high-risk MGUS (M spike ≥ 1.5 g/dL and/or non-IgG spike) were significantly more likely to have a diagnosis of SMM preceding symptomatic MM. In addition, patients with high-risk MGUS had a 3-fold higher probability of being diagnosed with symptomatic MM secondary to abnormal laboratory findings compared with low-risk MGUS patients (21% vs 7%). MM diagnosis secondary to onset of MM-related complications or incidental findings was less likely for high-risk patients than low-risk patients (40% vs 52% and 8% vs 19%, respectively).

NA indicates not applicable.

*

Statistically significant.

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