Microvascular Perfusion MRI Improves Therapy Monitoring and Detects Early Recurrences of Gliomas: A Large-Scale Trial

Andreas Stadlbauer1,2,3, Katarina Nikolic4,5, Franz Marhold4,6

  • 1From the Institute of Medical Radiology (A.S., K.N., F.M., A.Ö., G.H., S.O.), Karl Landsteiner University of Health Sciences, Krems, Austria andi@nmr.at.

Abstract

Insights

Microvascular perfusion (µPerf) MRI detects glioma recurrence earlier and more accurately than conventional MRI (cMRI). This advanced technique identifies subtle vascular changes, improving patient treatment strategies and outcomes.

Area of Science:

  • Neuroimaging
  • Oncology
  • Radiology

Background:

  • Detecting glioma recurrence is critical for patient outcomes but often limited by conventional MRI (cMRI) techniques.
  • Diagnostic uncertainty in glioma recurrence impacts therapeutic intervention decisions.
  • Subtle vascular changes preceding macroscopic tumor growth are key indicators of early recurrence.

Purpose of the Study:

  • To evaluate the efficacy of a microvascular perfusion (µPerf) imaging technique in detecting glioma recurrence.
  • To compare the diagnostic performance of µPerf with conventional MRI (cMRI) for early glioma recurrence detection.
  • To characterize subtle vascular changes indicative of early glioma recurrence using µPerf.

Main Methods:

  • Retrospective analysis of 351 patients with gliomas, with 422 follow-up MRI examinations undergoing quantitative analysis.
  • Standard cMRI protocol augmented with a 2-minute µPerf acquisition using spin-echo DSC perfusion MRI.
  • Generation of microvascular cerebral blood volume (CBV) and type indicator maps using custom Matlab software.
  • Comparison of µPerf findings with consensus radiologic interpretations of cMRI data by board-certified radiologists.
  • Statistical analysis including diagnostic performance metrics and AUROC for recurrence detection.

Main Results:

  • µPerf demonstrated superior diagnostic performance with 97.4% accuracy and AUROC values of 0.987 (type indicator) and 0.982 (CBV), significantly outperforming cMRI (85.1% accuracy, 0.941 AUROC).
  • µPerf identified glioma recurrence 41-353 days earlier than cMRI in 13.5% of cases, with a mean lead time of 137 days.
  • Early recurrences, particularly in high-grade gliomas, were primarily characterized by microvascular changes detected by µPerf.

Conclusions:

  • µPerf significantly improves the early detection of glioma recurrence compared to cMRI, showing higher sensitivity to microvascular changes.
  • The technique holds potential for more timely and personalized treatment strategies, potentially improving patient outcomes.
  • Further validation through multicenter studies and long-term outcome analyses is required for clinical integration.