Monoclonal gammopathy of undetermined significance and smouldering multiple myeloma: emphasis on risk factors for progression

RA Kyle, SV Rajkumar - British journal of haematology, 2007 - Wiley Online Library
British journal of haematology, 2007Wiley Online Library
Monoclonal gammopathy of undetermined significance (MGUS) is characterized by a serum
monoclonal protein< 30 g/l,< 10% plasma cells in the bone marrow, and absence of end‐
organ damage (CRAB–hyper c alcaemia, r enal insufficiency, a naemia, or b one lesions).
MGUS is present in 3% of persons> 50 years and in 5%> 70 years of age. The risk of
progression to multiple myeloma (MM) or a related disorder is 1% per year. Patients with risk
factors consisting of an abnormal serum free light chain ratio, non‐immunoglobulin G (IgG) …
Summary
Monoclonal gammopathy of undetermined significance (MGUS) is characterized by a serum monoclonal protein <30 g/l, <10% plasma cells in the bone marrow, and absence of end‐organ damage (CRAB–hypercalcaemia, renal insufficiency, anaemia, or bone lesions). MGUS is present in 3% of persons >50 years and in 5% >70 years of age. The risk of progression to multiple myeloma (MM) or a related disorder is 1% per year. Patients with risk factors consisting of an abnormal serum free light chain ratio, non‐immunoglobulin G (IgG) MGUS, and an elevated serum M protein ≥15 g/l had a risk of progression at 20 years of 58%, compared with 37% with two risk factors present, 21% with one risk factor present, and 5% when none of the risk factors were present. Smouldering (asymptomatic) multiple myeloma is characterized by having a serum IgG or IgA monoclonal protein of 30 g/l or higher and/or 10% or more plasma cells in the bone marrow but no evidence of end‐organ damage. The cumulative probability of progression to active MM or amyloidosis was 51% at 5 years, 66% at 10 years and 73% at 15 years; the median time to progression was 4·8 years.
Wiley Online Library