Abstract
Monoclonal gammopathy of undetermined significance (MGUS) that presents with no quantifiable M spike on immunofixation electrophoresis (IFE) can be termed IFE MGUS. We retrospectively identified patients with IFE MGUS who were monitored with at least 1 subsequent assessment that included an IFE, and evaluated the persistence of the monoclonal protein and the progression of disease. Although the monoclonal proteins persisted in the majority of patients, 16% did not experience this persistence, and had no documented immunomodulatory therapy. After a median follow-up of 3.9 years, the disease clinically progressed in 14 patients (3.2%). Eight of these 14 patients with clinical progression had an immunoglobulin (Ig) A IFE M protein and 6 had an IgG M protein. This study demonstrates that in some patients with IFE MGUS, the M proteins are transient and that IgA IFE MGUS is more likely to persist and progress to myeloma. © American Society for Clinical Pathology.
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Murray, D. L., Seningen, J. L., Dispenzieri, A., Snyder, M. R., Kyle, R. A., Rajkumar, S. V., & Katzmann, J. A. (2012). Laboratory persistence and clinical progression of small monoclonal abnormalities. American Journal of Clinical Pathology, 138(4), 609–613. https://doi.org/10.1309/AJCPT6OWWMHITA1Y
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