Intraoperative microscopic autofluorescence detection and characterization in brain tumors using stimulated Raman histology and two-photon fluorescence

• Verfasst von: Fürtjes, Gina [VerfasserIn]
• Verfasst von: Reinecke, David [VerfasserIn]
• Verfasst von: Spreckelsen, Niklas von [VerfasserIn]
• Verfasst von: Meißner, Anna-Katharina [VerfasserIn]
• Verfasst von: Rueß, Daniel Friedrich [VerfasserIn]
• Verfasst von: Timmer, Marco [VerfasserIn]
• Verfasst von: Freudiger, Christian [VerfasserIn]
• Verfasst von: Ion-Margineanu, Adrian [VerfasserIn]
• Verfasst von: Khalid, Florian [VerfasserIn]
• Verfasst von: Watrinet, Konstantin [VerfasserIn]
• Verfasst von: Mawrin, Christian [VerfasserIn]
• Verfasst von: Chmyrov, Andriy [VerfasserIn]
• Verfasst von: Goldbrunner, Roland [VerfasserIn]
• Verfasst von: Bruns, Oliver [VerfasserIn]
• Verfasst von: Neuschmelting, Volker [VerfasserIn]
• Titel: Intraoperative microscopic autofluorescence detection and characterization in brain tumors using stimulated Raman histology and two-photon fluorescence
• Verf.angabe: Gina Fürtjes, David Reinecke, Niklas von Spreckelsen, Anna-Katharina Meißner, Daniel Rueß, Marco Timmer, Christian Freudiger, Adrian Ion-Margineanu, Florian Khalid, Konstantin Watrinet, Christian Mawrin, Andriy Chmyrov, Roland Goldbrunner, Oliver Bruns and Volker Neuschmelting
• E-Jahr: 2023
• Jahr: 10 May 2023
• Umfang: 12 S.
• Fussnoten: Gesehen am 07.08.2023
• Titel Quelle: Enthalten in: Frontiers in oncology
• Ort Quelle: Lausanne : Frontiers Media, 2011
• Jahr Quelle: 2023
• Band/Heft Quelle: 13(2023), Artikel-ID 1146031, Seite 1-12
• ISSN Quelle: 2234-943X
• DOI: doi:10.3389/fonc.2023.1146031
• Datenträger: Online-Ressource
• Sprache: eng
• K10plus-PPN: 1854431943

Abstract

IntroductionThe intrinsic autofluorescence of biological tissues interferes with the detection of fluorophores administered for fluorescence guidance, an emerging auxiliary technique in oncological surgery. Yet, autofluorescence of the human brain and its neoplasia is sparsely examined. This study aims to assess autofluorescence of the brain and its neoplasia on a microscopic level by stimulated Raman histology (SRH) combined with two-photon fluorescence.MethodsWith this experimentally established label-free microscopy technique unprocessed tissue can be imaged and analyzed within minutes and the process is easily incorporated in the surgical workflow. In a prospective observational study, we analyzed 397 SRH and corresponding autofluorescence images of 162 samples from 81 consecutive patients that underwent brain tumor surgery. Small tissue samples were squashed on a slide for imaging. SRH and fluorescence images were acquired with a dual wavelength laser (790 nm and 1020 nm) for excitation. In these images tumor and non-tumor regions were identified by a convolutional neural network that reliably differentiates between tumor, healthy brain tissue and low quality SRH images. The identified areas were used to define regions.of- interests (ROIs) and the mean fluorescence intensity was measured.ResultsIn healthy brain tissue, we found an increased mean autofluorescence signal in the gray (11.86, SD 2.61, n=29) compared to the white matter (5.99, SD 5.14, n=11, p<0.01) and in the cerebrum (11.83, SD 3.29, n=33) versus the cerebellum (2.82, SD 0.93, n=7, p<0.001), respectively. The signal of carcinoma metastases, meningiomas, gliomas and pituitary adenomas was significantly lower (each p<0.05) compared to the autofluorescence in the cerebrum and dura, and significantly higher (each p<0.05) compared to the cerebellum. Melanoma metastases were found to have a higher fluorescent signal (p<0.01) compared to cerebrum and cerebellum.DiscussionIn conclusion we found that autofluorescence in the brain varies depending on the tissue type and localization and differs significantly among various brain tumors. This needs to be considered for interpreting photon signal during fluorescence-guided brain tumor surgery.