Liu Caidong, Chen Hongling, Sun Tong, Wang Haibo, Chen Baoan, Wang Xuerong
Department of Laboratory Medicine, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu Province, 210006 China.
Department of Pharmacology, Nanjing Medical University, Nanjing, Jiangsu Province, 210029 China.
Transl Oncol. 2021 May;14(5):101052. doi: 10.1016/j.tranon.2021.101052. Epub 2021 Mar 2.
Circulating cancer cells (CTCs) can serve as a non-invasive liquid biopsy and provide opportunities for early cancer diagnosis and evaluation. However, the value of CTCs for diagnosis or prognosis of small pulmonary nodules (SPNs) is unclear. Fifty-three patients diagnosed with SPNs with a diameter less than 30 mm by CT examination were enrolled in the study. The CTC numbers, CT examination features, serum tumor marker concentrations, and histopathological characteristics were analyzed. Centromere probe 8 (CEP8) was used as a marker for CTC identification. The CTC numbers were significantly different in patients with malignant and benign SPNs and with early (0/Ⅰa) and advanced (Ⅰb/Ⅱ/Ⅲ) lung cancer stages. ROC analysis showed that the CTC numbers was effective on malignant SNP diagnosis. The combined use of CTCs and the density features of the nodules determined by CT further improved the overall screening, the diagnostic effectiveness for malignant SNPs, and determination of the pTNM (≤Ia vs.>Ia) stage. The CT morphology revealed that large, single, and solid SPNs were associated with significant CTC numbers and the CTC numbers were correlated with malignant histopathology. Using CEP8 as a marker resulted in detection of more CTC numbers in 22 patient samples triple stained for CEP8, EpCAM, and CKs. The CTCs determined by CEP8-positive staining could serve as potential screening and diagnostic markers for malignant SPNs.
循环肿瘤细胞(CTCs)可作为一种非侵入性液体活检手段,为癌症早期诊断和评估提供契机。然而,CTCs对小肺结节(SPNs)诊断或预后的价值尚不清楚。本研究纳入了53例经CT检查诊断为直径小于30mm的SPNs患者。分析了CTCs数量、CT检查特征、血清肿瘤标志物浓度及组织病理学特征。着丝粒探针8(CEP8)用作CTCs识别的标志物。恶性和良性SPNs患者以及早期(0/Ⅰa期)和晚期(Ⅰb/Ⅱ/Ⅲ期)肺癌患者的CTCs数量存在显著差异。ROC分析表明,CTCs数量对恶性SPN诊断有效。CTCs与CT确定的结节密度特征联合使用进一步提高了整体筛查、恶性SPN的诊断效能以及pTNM(≤Ia期与>Ia期)分期的判定。CT形态显示,大的、单发的实性SPNs与显著的CTCs数量相关,且CTCs数量与恶性组织病理学相关。以CEP8作为标志物,在22例对CEP8、EpCAM和细胞角蛋白进行三重染色的患者样本中检测到更多的CTCs数量。CEP8阳性染色确定的CTCs可作为恶性SPNs潜在的筛查和诊断标志物。