Raman hyperspectral imaging coupled to three-dimensional discriminant analysis: classification of meningiomas brain tumour grades

Lilo, Taha Luay, Medeiros-De-morais, Camilo De lelis orcid iconORCID: 0000-0003-2573-787X, Ashton, Katherine M., Davis, Charles, Dawson, Timothy P., Martin, Francis L., Alder, Jane Elizabeth orcid iconORCID: 0000-0003-4463-0349, Roberts, Gareth, Ray, Arup et al (2022) Raman hyperspectral imaging coupled to three-dimensional discriminant analysis: classification of meningiomas brain tumour grades. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy . ISSN 1386-1425

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Official URL: https://doi.org/10.1016/j.saa.2022.121018

Abstract

Meningiomas remains a clinical dilemma. They are the commonest “benign” types of brain tumours and, although being typically benign, they are divided into three WHO grades categories (I, II and III) which are associated with the tumour growth rate and likelihood of recurrence. Recurrence depends on extend of surgery as well as histopathological diagnosis. There is a marked variation amongst surgeons in the follow-up arrangements for their patients even within the same unit which has a significant clinical, and financial implication. Knowing the tumour grade rapidly is an important factor to predict surgical outcomes and adequate patient treatment. Clinical follow up sometimes is haphazard and not based on clear evidence. Spectrochemical techniques are a powerful tool for cancer diagnostics. Raman hyperspectral imaging is able to generate spatially-distributed spectrochemical signatures with great sensitivity. Using this technique, 95 brain tissue samples (66 meningiomas WHO grade I, 24 meningiomas WHO grade II and 5 meningiomas that reoccurred) were analysed in order to discriminate grade I and grade II samples. Newly-developed three-dimensional discriminant analysis algorithms were used to process the hyperspectral imaging data in a 3D fashion. Three-dimensional principal component analysis quadratic discriminant analysis (3D-PCA-QDA) was able to distinguish grade I and grade II meningioma samples with 96% test accuracy (100% sensitivity and 95% specificity). This technique is here shown to be a high-throughput, reagent-free, non-destructive, and can give accurate predictive information regarding the meningioma tumour grade, hence, having enormous clinical potential with regards to being developed for intra-operative real-time assessment of disease.


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