Intraoperative detection of IDH-mutant glioma using fluorescence lifetime imaging.
Silvia Noble AnbunesanAlba Alfonso-GarciaXiangnan ZhouJulien BecHan Sung LeeLee-Way JinOrin BlochLaura MarcuPublished in: Journal of biophotonics (2022)
Identifying isocitrate dehydrogenase (IDH)-mutation and glioma subtype during surgery instead of days later can aid in modifying tumor resection strategies for better survival outcomes. We report intraoperative identification of IDH-mutant glioma (N = 12 patients) with a clinically compatible fluorescence lifetime imaging (FLIm) device (excitation: 355 nm; emission spectral bands: 390/40 nm, 470/28 nm, 542/50 nm). The fluorescence-derived parameters were analyzed to study the optical contrast between IDH-mutant tumors and surrounding brain tissue. IDH-mutant oligodendrogliomas exhibited shorter lifetimes (3.3 ± 0.1 ns) than IDH-mutant astrocytomas (4.1 ± 0.1 ns). Both IDH-mutant glioma subtypes had shorter lifetimes than white matter (4.6 ± 0.4 ns) but had comparable lifetimes to cortex. Lifetimes also increased with malignancy grade within IDH-mutant oligodendrogliomas (grade 2: 2.96 ± 0.08 ns, grade 3: 3.4 ± 0.3 ns) but not within IDH-mutant astrocytomas. The current results support the feasibility of FLIm as a surgical adjuvant for identifying IDH-mutant glioma tissue.
Keyphrases
- wild type
- low grade
- dengue virus
- white matter
- photodynamic therapy
- high resolution
- minimally invasive
- magnetic resonance
- patients undergoing
- high grade
- multiple sclerosis
- coronary artery disease
- blood brain barrier
- mass spectrometry
- atrial fibrillation
- functional connectivity
- optical coherence tomography
- zika virus
- contrast enhanced
- resting state
- light emitting