Dynamic contrast-enhanced magnetic resonance imaging identifies a subgroup of patients with asymptomatic monoclonal

Jens Hillengass1, Christian Zechmann, Tobias Bäuerle

  • 1German Cancer Research Center, Department of Radiology; University of Heidelberg, Department of Hematology, Oncology and Rheumatology, Heidelberg, Germany. Jens.Hillengass@med.uni-heidelberg.de

Abstract

Insights

Dynamic contrast-enhanced MRI reveals increasing microcirculation in plasma cell diseases. This imaging technique can identify patients with early or advanced multiple myeloma and monoclonal gammopathy of undetermined significance who may have poorer prognoses.

Area of Science:

  • Biomedical Imaging
  • Oncology
  • Radiology

Background:

  • Plasma cell disorders, including monoclonal gammopathy of undetermined significance (MGUS) and multiple myeloma (MM), are characterized by the proliferation of malignant plasma cells.
  • Understanding the microcirculatory changes associated with disease progression is crucial for diagnosis and prognosis.

Purpose of the Study:

  • To evaluate the utility of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) in visualizing microcirculatory alterations.
  • To differentiate between healthy individuals and patients with early (MGUS, asymptomatic MM) and advanced (symptomatic MM) plasma cell diseases based on microcirculation parameters.

Main Methods:

  • A cohort of 222 individuals, including healthy controls and patients with MGUS, asymptomatic MM (aMM), and symptomatic MM (sMM), underwent lumbar spine DCE-MRI.
  • Microcirculation parameters, specifically amplitude A (vascular volume) and exchange rate constant kep (permeability), were quantified.

Main Results:

  • A continuous increase in microcirculation parameters (A and kep) was observed from healthy controls to MGUS, aMM, and sMM.
  • Significant differences in A and kep were found between controls and aMM/sMM (P < 0.05).
  • Focal hotspots in microcirculation patterns were exclusively detected in sMM (42.6%) and rarely in MGUS/aMM, correlating with higher bone marrow plasmocytosis.

Conclusions:

  • DCE-MRI findings support the concept of an angiogenic switch during plasma cell disease progression.
  • Pathologic DCE-MRI findings correlate with adverse prognostic factors.
  • DCE-MRI can identify a distinct subgroup of MGUS and aMM patients with increased microcirculation, suggesting potential for early risk stratification.