Approximately 20% of patients with multiple myeloma are recognized by
chance without significant symptoms. In order to prevent morbidity wit
h timely therapy, reliable criteria are needed that distinguish those
likely to show early or late disease progression. Multiple clinical fe
atures were assessed in 101 consecutive, asymptomatic and previously u
ntreated patients. Patients with one or more lytic bone lesions were e
xcluded because this feature had been found previously to be associate
d with early progression. Multivariate analysis indicated that only se
rum myeloma globulin >30 g/l, IgA protein type, and Bence Jones protei
n excretion >50mg/d remained as significant independent variables. The
presence of two or more of these features signified high-risk disease
with early progression (median 17 months) whereas the absence of any
adverse variable was associated with prolonged stability (median 95 mo
nths) (P < 0.01). Magnetic resonance (MR) imaging of the spine was use
ful only in patients with one adverse feature and an intermediate time
to progression (median 39 months). An abnormal pattern (40% of patien
ts) helped to distinguish patients with an imminent complication from
those with more stable disease, Because a serious complication (fractu
re, hypercalcaemia) occurred in 35% of patients with early disease pro
gression, chemotherapy seems justified for selected patients with asym
ptomatic disease at diagnosis. The remaining patients were at such low
risk for progression (median 6 years) that they may be followed safel
y at long intervals without treatment.