Real-time in vivo cancer staging of nasopharyngeal carcinoma patients with rapid fiberoptic Raman endoscopy

被引:6
|
作者
Shu, Chi [1 ]
Zheng, Wei [1 ]
Lin, Kan [1 ]
Lim, Chwee Ming [2 ]
Huang, Zhiwei [1 ,3 ]
机构
[1] Natl Univ Singapore, Coll Design & Engn, Dept Biomed Engn, Opt Bioimaging Lab, Singapore 117576, Singapore
[2] Singapore Gen Hosp, Duke NUS Grad Med Sch, Dept Otolaryngol, Singapore 169608, Singapore
[3] Natl Univ Singapore, Coll Design & Engn, Dept Biomed Engn, Opt Bioimaging Lab, 9 Engn Dr 1, Singapore 117576, Singapore
基金
英国医学研究理事会;
关键词
Fiberoptic Raman spectroscopy; Nasopharyngeal carcinoma; Cancer staging; DIAGNOSIS; SPECTROSCOPY; SYSTEM; DYSPLASIA; EDITION; PROBE;
D O I
10.1016/j.talanta.2023.124561
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Cancer staging is important to guide treatment and for prognostication. This work aims to demonstrate the ability of rapid fiberoptic Raman endoscopy for real-time in vivo cancer staging of nasopharyngeal cancer (NPC) patients. We interrogate 278 tissue sites on the primary NPC with different cancer stages from 61 NPC patients and 50 healthy volunteers using rapid fiberoptic Raman endoscopy examination. Distinct Raman spectral dif-ferences of NPC at different cancer stages are observed through simultaneous fingerprint and high-wavenumber (FP/HW) Raman spectral measurements, reflecting the biomolecular differences of NPC tumor across various cancer stages. Raman staging model is established based on in vivo FP/HW tissue Raman spectra together with partial-least-squares linear-discriminant-analysis (PLS-LDA) and leave-one-tissue-site-out cross-validation (LOOCV). In vivo FP/HW Raman endoscopy provides an overall diagnostic accuracy of 92.81% for identifying different stages of NPC (i.e., NPC stage I&II and NPC stage III&IV) from normal nasopharynx. Specifically, the diagnostic sensitivity of 91.18% is obtained for identifying NPC stage I& II; and the sensitivity of 93.04% is achieved for classifying NPC stage III&IV from normal tissue. The key tissue biomolecular variations responsible for different NPC stages have been identified using biomolecular Raman modeling developed based on non-negative linear regression. The essential biomolecules (chondroitin sulfate, glucose, hemoglobin, oleic acid and triolein) are uncovered from the Raman spectra of NPC tissues through biomolecular modeling with sig-nificant variations (p < 0.05) between early-stage NPC (stage I and stage II) and late-stage NPC patients (stage III and stage IV). Our pivotal work demonstrates for the first time that fiberoptic Raman endoscopy is a robust analytical tool for real-time in vivo NPC staging in clinical settings.
引用
收藏
页数:7
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