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Abstract

The purpose of this study was to define the risk of progression and survival of patients with Smoldering Waldenstrom's Macroglobulinemia (SWM). SWM is defined clinically as having a serum monoclonal IgM protein ≥ 3 g/dL and/or ≥ 10% bone marrow lymphoplasmacytic infiltration but no evidence of end-organ damage (anemia, constitutional symptoms, hyperviscosity, lymphadenopathy or hepatosplenomegaly). We searched a computerized database and reviewed the medical records of all patients at Mayo Clinic who fulfilled the criteria of SWM between 1974 and 1995. During 285 cumulative person-years of follow-up of the 48 patients with SWM (median, 15.4 years), 34 (71%) progressed to symptomatic Waldenstrom's Macroglobulinemia (WM) requiring treatment, 1 to AL amyloidosis and 1 to lymphoma (total, 75%). The cumulative probability of progression to symptomatic WM, amyloidosis or lymphoma was 6% at 1 year, 39% at 3 years, 59% at 5 years and 68% at 10 years. The major risk factors for progression were percentage of lymphoplasmacytic cells in the bone marrow, size of the serum M-spike and the hemoglobin value. Patients with SWM should be followed and not treated until symptomatic WM develops. Treatment on a clinical trial for those at greatest risk of progression should be considered.

  • Submitted October 11, 2011.
  • Accepted March 13, 2012.