循环肿瘤细胞
多路复用
液体活检
医学
肺癌
癌症
微流控
癌症研究
阶段(地层学)
肿瘤科
活检
病理
生物医学工程
生物标志物
癌细胞
细胞
疾病监测
全血
免疫荧光
内科学
作者
Ebru Özgür,Ayça Çırçır,B. Dogan,Sebnem M. Sahin,Gizem Karayalçın,Mehmet Alper Demir,Başak Erkek,Enes Demirtaş,Özge Zorlu,Furkan Ceylan,Haluk Külah,Nuri Karadurmuş,Mehmet Ali Nahit Şendur,S. Kılıçkap
出处
期刊:Biosensors
[Multidisciplinary Digital Publishing Institute]
日期:2026-01-02
卷期号:16 (1): 34-34
摘要
Lung cancer is the leading cause of cancer-related mortality worldwide, with non-small-cell lung cancer (NSCLC) accounting for the majority of cases. Standard tissue biopsies are invasive and unsuitable for repeated monitoring. Liquid biopsy technologies, particularly circulating tumor cell (CTC) analysis, offer a minimally invasive alternative for real-time disease tracking. To address the need for efficient and reproducible CTC isolation, we developed the Cellsway microfluidic CTC enrichment and identification platform, which employs inertial hydrodynamics in a spiral-shaped microfluidic channel comprising hydrofoil-shaped pillars to enable high-throughput, label-free enrichment of CTCs while preserving cell integrity, followed by an optimized CTC identification assay. Analytical performance assessed through spiking experiments using NSCLC cell lines demonstrated recovery rates of 91.9% for H1975 cells and 78.3% for A549 cells. Clinical validation was performed on blood samples from 51 stage IV NSCLC patients. A 7.5 mL volume of peripheral blood was processed with the SwayBox platform, and enriched CTCs were identified through an optimized multiplex immunofluorescence protocol. CTCs were detected in 47% of NSCLC patients, with counts ranging from 0 to 72 cells per 7.5 mL of blood. At a cutoff of 1 CTC per 7.5 mL, the assay achieved a specificity of 95%. Patient-derived CTCs exhibited smaller mean diameters compared to cultured NSCLC cell lines, yet were effectively enriched through hydro-dynamic tuning. These findings demonstrate that the Cellsway platform enables efficient and re-producible CTC isolation with high specificity, supporting its potential utility for clinical monitoring and precision oncology in NSCLC.
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