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The Oncologist, Vol. 1, No. 5, 315–323, October 1996
© 1996 AlphaMed Press


MEET THE PROFESSOR

Multiple Myeloma: An Overview in 1996

Robert A. Kyle

Division of Hematology and Internal Medicine, Mayo Clinic and Mayo Foundation, Rochester, Minnesota, USA

Correspondence: R.A. Kyle, M.D., Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

Multiple myeloma (MM) has an incidence of approximately four per 100,000 per year. Ninety-nine percent of patients with MM have a monoclonal (M-) protein in the serum or urine during the course of their disease. MM must be differentiated from smoldering multiple myeloma (SMM), which has an M-protein value of more than 30 g/l and more than 10% plasma cells in the bone marrow, but no other features of MM. The plasma cell labeling index (PCLI) and the presence of circulating plasma cells in the peripheral blood help to differentiate monoclonal gammopathy of undetermined significance and SMM from MM. The current median duration of survival with chemotherapy is about three years. Patients with low PCLI and low ß2-microglobulin values have a median duration of survival of approximately six years. Melphalan and prednisone produce an objective response in 50% to 60% of patients. Combinations of chemotherapy produce a higher response rate, but the survival rate is not different. Allogeneic bone marrow transplantation is associated with a mortality rate of 25% within six months and an actuarial survival rate of 28% at seven years. Autologous peripheral stem cell transplantation is applicable to more patients and is reported to produce a higher response rate and longer survival than chemotherapy, but most patients will eventually have relapse.

Key Words. Differential diagnosis • Multiple myeloma • Allogeneic transplantation • Autologous transplantation • Treatment




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L. Wang and D. C. Young
Suppression of Polyclonal Immunoglobulin Production by M-proteins Shows Isotype Specificity
Ann. Clin. Lab. Sci., July 1, 2001; 31(3): 274 - 278.
[Abstract] [Full Text] [PDF]




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