| Literature DB >> 26468325 |
Minbiao Ji1, Spencer Lewis2, Sandra Camelo-Piragua3, Shakti H Ramkissoon4, Matija Snuderl5, Sriram Venneti3, Amanda Fisher-Hubbard3, Mia Garrard2, Dan Fu1, Anthony C Wang2, Jason A Heth2, Cormac O Maher2, Nader Sanai6, Timothy D Johnson7, Christian W Freudiger8, Oren Sagher2, Xiaoliang Sunney Xie9, Daniel A Orringer10.
Abstract
Differentiating tumor from normal brain is a major barrier to achieving optimal outcome in brain tumor surgery. New imaging techniques for visualizing tumor margins during surgery are needed to improve surgical results. We recently demonstrated the ability of stimulated Raman scattering (SRS) microscopy, a nondestructive, label-free optical method, to reveal glioma infiltration in animal models. We show that SRS reveals human brain tumor infiltration in fresh, unprocessed surgical specimens from 22 neurosurgical patients. SRS detects tumor infiltration in near-perfect agreement with standard hematoxylin and eosin light microscopy (κ = 0.86). The unique chemical contrast specific to SRS microscopy enables tumor detection by revealing quantifiable alterations in tissue cellularity, axonal density, and protein/lipid ratio in tumor-infiltrated tissues. To ensure that SRS microscopic data can be easily used in brain tumor surgery, without the need for expert interpretation, we created a classifier based on cellularity, axonal density, and protein/lipid ratio in SRS images capable of detecting tumor infiltration with 97.5% sensitivity and 98.5% specificity. Quantitative SRS microscopy detects the spread of tumor cells, even in brain tissue surrounding a tumor that appears grossly normal. By accurately revealing tumor infiltration, quantitative SRS microscopy holds potential for improving the accuracy of brain tumor surgery.Entities:
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Year: 2015 PMID: 26468325 PMCID: PMC4900155 DOI: 10.1126/scitranslmed.aab0195
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956