Intraoperative brain tumor classification via laser-induced fluorescence spectroscopy and machine learning

离体 医学 胶质瘤 荧光团 体内 接收机工作特性 垂体腺瘤 腺瘤 病理 核医学 人工智能 荧光 计算机科学 内科学 癌症研究 生物 光学 物理 生物技术
作者
Tanner J. Zachem,Jacob Sperber,Sully F. Chen,Syed M. Adil,Benjamin D. Wissel,Gregory Chamberlin,Edwin Owolo,Annee Nguyen,Kerri‐Anne Crowell,James E. Herndon,Ralph Abi Hachem,David W. Jang,Thomas J. Cummings,Margaret Johnson,William C. Eward,Anoop P. Patel,Jordan Komisarow,Steven Cook,Derek G. Southwell,Peter E. Fecci
出处
期刊:Journal of Neurosurgery [American Association of Neurological Surgeons]
卷期号:: 1-10
标识
DOI:10.3171/2024.12.jns242041
摘要

OBJECTIVE To optimize neurosurgical tumor resection, tissue types and borders must be appropriately identified. Authors of this study established the use of a nondestructive laser-based endogenous fluorescence spectroscopy device, "TumorID," to almost immediately classify a specimen as glioma, meningioma, pituitary adenoma, or nonneoplastic tissue in the operating room, utilizing a machine learning algorithm. METHODS TumorID requires only 0.5 seconds to collect data, without the need for any dyes or tissue manipulation, and utilizes a 100-mW, 405-nm laser that does not damage the tissue. The system was used in the operating room to scan ex vivo specimens from 46 patients (mean age 52 years) with glioma (8 patients), meningioma (10 patients), pituitary adenoma (23 patients), and nonneoplastic tissue resected during an epilepsy operation (5 patients). A support vector machine algorithm was trained to distinguish between these lesions and classify them in near real time. Statistical significance was determined through a generalized estimating equation on the area under the known fluorophore emission regions for free reduced nicotinamide adenine dinucleotide (NADH), bound NADH, flavin adenine dinucleotide, and neutral porphyrins. RESULTS Ultimately, the machine learning model showed a high degree of classification power with a multiclass area under the receiver operating characteristic curve of 0.809 ± 0.002. The areas under the curve for neutral porphyrins were found to be statistically significant (p < 0.001) and to have the largest impact on model output. CONCLUSIONS This initial ex vivo clinical study demonstrated the ability of TumorID to rapidly differentiate and classify various pathologies and surrounding brain in a configuration that can be easily translated to scan in vivo. This classification power could allow TumorID to augment surgical decision-making by enabling rapid intraoperative tissue diagnostics and border delineation, potentially improving patient outcomes by allowing for a more informed and complete resection.
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