Smouldering myeloma

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Smouldering myeloma
Other namesSmoldering myeloma, Smoldering multiple myeloma, Indolent myeloma or Asymptomatic myeloma
SpecialtyHematology/oncology

Smouldering myeloma is a disease classified as intermediate in a spectrum of step-wise progressive diseases termed

pre-malignant disease that lacks symptoms but is associated with bone marrow biopsy showing the presence of an abnormal number of clonal myeloma cells, blood and/or urine containing a myeloma protein, and a significant risk of developing into a malignant disease.[2]

Diagnosis

Smouldering myeloma is characterised by:[4]

  • Serum paraprotein >30 g/L or urinary monoclonal protein ≥500 mg per 24 h AND/OR
  • Clonal plasma cells >10% and <60% on bone marrow biopsy AND
  • No evidence of end organ damage that can be attributed to plasma cell disorder AND
  • No myeloma-defining event (>60% plasma cells in bone marrow OR Involved/Uninvolved light chain ratio>100)

Treatment

Treatment for multiple myeloma is focused on therapies that decrease the clonal plasma cell population and consequently decrease the signs and symptoms of disease. If the disease is completely asymptomatic (i.e. there is a paraprotein and an abnormal bone marrow population but no end-organ damage), as in smouldering myeloma, treatment is typically deferred, or restricted to clinical trials.[5]

They are generally responsive to

IL-1β neutralisation.[6]

Prognosis

Smouldering myeloma with an increasingly abnormal serum free light chain (FLC) ratio is associated with a higher risk for progression to active multiple myeloma.[7]

References

Further reading