A long-term study of prognosis in monoclonal gammopathy of undetermined significance.

BACKGROUND A monoclonal gammopathy of undetermined significance (MGUS) occurs in up to 2 percent of persons 50 years of age or older. Reliable predictors of progression have not been identified, and information on prognosis is limited. METHODS We identified 1384 patients residing in southeastern Minnesota in whom MGUS was diagnosed at the Mayo Clinic from 1960 through 1994. The primary end point was progression to multiple myeloma or another plasma-cell cancer. RESULTS During 11,009 person-years of follow-up, MGUS progressed in 115 of the 1384 patients to multiple myeloma, IgM lymphoma, primary amyloidosis, macroglobulinemia, chronic lymphocytic leukemia, or plasmacytoma (relative risk of progression, 25.0, 2.4, 8.4, 46.0, 0.9, and 8.5, respectively). The overall relative risk of progression was 7.3 in these patients as compared with the white population of the Iowa Surveillance, Epidemiology, and End Results program. In 32 additional patients, the monoclonal protein concentration increased to more than 3 g per deciliter or the percentage of plasma cells in the bone marrow increased to more than 10 percent (smoldering multiple myeloma) but without progression to overt myeloma or related disorders. The cumulative probability of progression was 12 percent at 10 years, 25 percent at 20 years, and 30 percent at 25 years. The initial concentration of serum monoclonal protein was a significant predictor of progression at 20 years. CONCLUSIONS The risk of progression of MGUS to multiple myeloma or related disorders is about 1 percent per year.

[1]  A. López-Guillermo,et al.  Malignant transformation and life expectancy in monoclonal gammopathy of undetermined significance , 1992, British journal of haematology.

[2]  J Crowley,et al.  Estimation of failure probabilities in the presence of competing risks: new representations of old estimators. , 1999, Statistics in medicine.

[3]  J. Peto,et al.  Asymptotically Efficient Rank Invariant Test Procedures , 1972 .

[4]  U. Axelsson,et al.  Frequency of pathological proteins (M-components) om 6,995 sera from an adult population. , 2009, Acta medica Scandinavica.

[5]  M. Vicariot,et al.  Monoclonal gammopathies in the adult population of Finistère, France. , 1982, Journal of clinical pathology.

[6]  R. Kyle,et al.  Monoclonal gammopathy of undetermined significance. Natural history in 241 cases. , 1978, The American journal of medicine.

[7]  A. Linos,et al.  Incidence and natural history of primary systemic amyloidosis in Olmsted County, Minnesota, 1950 through 1989. , 1992, Blood.

[8]  L. Melton,et al.  The threat to medical-records research. , 1997, The New England journal of medicine.

[9]  D. Cox Regression Models and Life-Tables , 1972 .

[10]  L. Elveback,et al.  Incidence of monoclonal proteins in a Minnesota community with a cluster of multiple myeloma. , 1972, Blood.

[11]  R A Kyle,et al.  "Benign" monoclonal gammopathy--after 20 to 35 years of follow-up. , 1993, Mayo Clinic proceedings.

[12]  L. Melton,et al.  History of the Rochester Epidemiology Project. , 1996, Mayo Clinic proceedings.

[13]  E. Kaplan,et al.  Nonparametric Estimation from Incomplete Observations , 1958 .

[14]  G Berry,et al.  The analysis of mortality by the subject-years method. , 1983, Biometrics.

[15]  L. Baldini,et al.  Role of different hematologic variables in defining the risk of malignant transformation in monoclonal gammopathy. , 1996, Blood.

[16]  J. Hällén Discrete gammaglobulin (M-)components in serum. Clinical study of 150 subjects without myelomatosis. , 1966, Acta medica Scandinavica. Supplementum.

[17]  J. Coebergh,et al.  Malignant transformation of monoclonal gammopathy of undetermined significance among out‐patients of a community hospital in Southeastern Netherlands , 1995, British journal of haematology.