Circulating microparticles of glial origin and tissue factor bearing in high-grade glioma: a potential prothrombotic

Maria Teresa Sartori1, Alessandro Della Puppa, Andrea Ballin

  • 1Department of Cardiologic, Thoracic and Vascular Sciences, via Giustiniani 2, Padua, Italy. mtsart@unipd.it

Insights

Circulating microparticles (MPs), particularly glial-derived and tissue factor-bearing MPs, are elevated in glioblastoma multiforme (GBM) patients and may predict venous thromboembolism (VTE) risk after treatment.

Area of Science:

  • Neuro-oncology
  • Hematology
  • Oncology

Background:

  • Glioblastoma multiforme (GBM) patients frequently experience venous thromboembolism (VTE).
  • Circulating microparticles (MPs) are implicated in cancer-associated VTE.
  • Understanding MP profiles in GBM may reveal VTE risk factors.

Purpose of the Study:

  • To investigate the association between circulating microparticle levels and VTE in glioblastoma patients.
  • To evaluate changes in MP numbers and procoagulant activity post-surgery and treatment.
  • To identify specific MP subsets that predict VTE risk in GBM.

Main Methods:

  • Prospective evaluation of 61 GBM patients undergoing surgery and radio-chemotherapy.
  • Measurement of microparticle numbers (glial-derived, endothelial, annexin V+, tissue factor-bearing) via flow cytometry.
  • Correlation analysis of MP levels with VTE development and clinical outcomes.

Main Results:

  • Baseline MP levels (GFAP+/TF-, TF+/GFAP-, GFAP+/TF+) were higher in GBM patients than controls.
  • MP levels increased post-surgery, with sustained elevation in subtotally resected cases.
  • Elevated TF+/GFAP- MPs were significantly associated with VTE development (p=0.04) and increased VTE risk (RR 4.17).

Conclusions:

  • Glial-derived and tissue factor-bearing MPs are elevated in GBM patients, persisting and increasing post-treatment.
  • Subtotal resection correlates with higher MP levels, potentially indicating disease progression.
  • Tissue factor-bearing/glial-derived MPs (TF+/GFAP-) are a potential biomarker for predicting VTE risk in glioblastoma.

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