The STEMRI trial: Magnetic resonance spectroscopy imaging can define tumor areas enriched in glioblastoma stem-like cells.
Anthony LemariéVincent LubranoCaroline DelmasAmélie LusqueJuan Pablo CerapioMarion PerrierAurore SiegfriedFlorent ArnauducYvan NicaisePerrine DahanThomas FilleronMuriel MounierChristine ToulasElizabeth Cohen-Jonathan MoyalPublished in: Science advances (2023)
Despite maximally safe resection of the magnetic resonance imaging (MRI)-defined contrast-enhanced (CE) central tumor area and chemoradiotherapy, most patients with glioblastoma (GBM) relapse within a year in peritumoral FLAIR regions. Magnetic resonance spectroscopy imaging (MRSI) can discriminate metabolic tumor areas with higher recurrence potential as CNI+ regions (choline/ N -acetyl-aspartate index >2) can predict relapse sites. As relapses are mainly imputed to glioblastoma stem-like cells (GSCs), CNI+ areas might be GSC enriched. In this prospective trial, 16 patients with GBM underwent MRSI/MRI before surgery/chemoradiotherapy to investigate GSC content in CNI-/+ biopsies from CE/FLAIR. Biopsy and derived-GSC characterization revealed a FLAIR/CNI+ sample enrichment in GSC and in gene signatures related to stemness, DNA repair, adhesion/migration, and mitochondrial bioenergetics. FLAIR/CNI+ samples generate GSC-enriched neurospheres faster than FLAIR/CNI-. Parameters assessing biopsy GSC content and time-to-neurosphere formation in FLAIR/CNI+ were associated with worse patient outcome. Preoperative MRI/MRSI would certainly allow better resection and targeting of FLAIR/CNI+ areas, as their GSC enrichment can predict worse outcomes.
Keyphrases
- contrast enhanced
- magnetic resonance imaging
- diffusion weighted
- dna repair
- diffusion weighted imaging
- computed tomography
- magnetic resonance
- high resolution
- stem cells
- rectal cancer
- oxidative stress
- clinical trial
- ultrasound guided
- locally advanced
- minimally invasive
- randomized controlled trial
- patients undergoing
- fine needle aspiration
- phase iii
- free survival
- radiation therapy
- gene expression
- coronary artery disease
- fluorescence imaging
- cancer therapy
- escherichia coli
- atrial fibrillation
- type diabetes
- copy number
- climate change
- single cell
- dna methylation
- signaling pathway
- dna damage response
- drug induced