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Quantitative fluorescence in intracranial tumor: implications for ALA-induced PpIX as an intraoperative biomarker

医学 原卟啉IX 胶质瘤 生物标志物 体内 病理 接收机工作特性 曲线下面积 转移 成像生物标志物 放射科 核医学 癌症 荧光 磁共振成像 内科学 癌症研究 化学 生物 生物化学 物理 生物技术 量子力学
作者
Pablo A. Valdés,Frédéric Leblond,Anthony Kim,Brent T. Harris,Brian C. Wilson,Xiaoyao Fan,Tor D. Tosteson,Alex Hartov,Songbai Ji,Kadir Erkmen,Nathan E. Simmons,Keith D. Paulsen,David W. Roberts
出处
期刊:Journal of Neurosurgery [Journal of Neurosurgery Publishing Group]
卷期号:115 (1): 11-17 被引量:300
标识
DOI:10.3171/2011.2.jns101451
摘要

Accurate discrimination between tumor and normal tissue is crucial for optimal tumor resection. Qualitative fluorescence of protoporphyrin IX (PpIX), synthesized endogenously following δ-aminolevulinic acid (ALA) administration, has been used for this purpose in high-grade glioma (HGG). The authors show that diagnostically significant but visually imperceptible concentrations of PpIX can be quantitatively measured in vivo and used to discriminate normal from neoplastic brain tissue across a range of tumor histologies.The authors studied 14 patients with diagnoses of low-grade glioma (LGG), HGG, meningioma, and metastasis under an institutional review board-approved protocol for fluorescence-guided resection. The primary aim of the study was to compare the diagnostic capabilities of a highly sensitive, spectrally resolved quantitative fluorescence approach to conventional fluorescence imaging for detection of neoplastic tissue in vivo.A significant difference in the quantitative measurements of PpIX concentration occurred in all tumor groups compared with normal brain tissue. Receiver operating characteristic (ROC) curve analysis of PpIX concentration as a diagnostic variable for detection of neoplastic tissue yielded a classification efficiency of 87% (AUC = 0.95, specificity = 92%, sensitivity = 84%) compared with 66% (AUC = 0.73, specificity = 100%, sensitivity = 47%) for conventional fluorescence imaging (p < 0.0001). More than 81% (57 of 70) of the quantitative fluorescence measurements that were below the threshold of the surgeon's visual perception were classified correctly in an analysis of all tumors.These findings are clinically profound because they demonstrate that ALA-induced PpIX is a targeting biomarker for a variety of intracranial tumors beyond HGGs. This study is the first to measure quantitative ALA-induced PpIX concentrations in vivo, and the results have broad implications for guidance during resection of intracranial tumors.
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