利用基于纳米的检测方法探索 II-IV 期结直肠癌循环肿瘤细胞的诊断和预后意义。

Gang Liu, Jinfeng Zhu, Pengbo Zhang, Tingting Zhang, Zheng Cui, Fanglei Jiao, Wenjun Le, Xiaofeng Li, Bingdi Chen
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引用次数: 0

摘要

背景:结直肠癌(CRC)是全球癌症死亡的主要原因之一,因此迫切需要一种无创、有效的生物标志物来改善患者的预后。循环肿瘤细胞(CTCs)是实时监测肿瘤的潜在标志物,但由于现有检测方法灵敏度低,其临床应用受到限制。此前,我们提出了一种基于纳米的新型 CTCs 检测方法,该方法依赖于细胞表面的电特性,因此无需特定的分子生物标记物。在本研究中,我们采用这种技术评估了 CTCs 在 II-IV 期 CRC 中的诊断和预后价值:方法:共纳入 194 名参与者,其中包括 136 名 CRC 患者和 58 名健康人。方法:共纳入 194 名参与者,包括 136 名 CRC 患者和 58 名健康人,采集参与者的外周血,利用我们新开发的基于纳米的检测方法对 CTCs 进行计数。我们采用受试者操作特征曲线(ROC)和多变量考克斯比例危险分析评估了CTCs在诊断CRC和预测患者预后方面的有效性:结果:基于纳米技术的方法能够将 CRC 患者与健康人区分开来,灵敏度为 84.6%,特异度为 94.8%。此外,基线 CTCs 水平还能预测 CRC 患者的无进展生存期(PFS),与较高水平相比,较低水平的 CTCs 会延长无进展生存期(15 CTCs/mL 时为 4.5 个月对 8.0 个月,p = 0.016;20 CTCs/mL 时为 4.4 个月对 8.0 个月,p = 0.028)。我们还探讨了化疗 1-5 个周期后 CTCs 数量的动态变化。CTCs 水平升高的患者通常会出现疾病进展(PD),而 CTCs 水平降低的患者通常会获得部分反应(PR)或保持疾病稳定(SD)。这些发现表明,CTCs 数量的动态波动与疾病的临床过程密切相关:我们的研究表明,基于纳米技术的 CTCs 检测具有诊断和预测 II-IV 期 CRC 患者预后的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring the diagnostic and prognostic significance of circulating tumor cells in stage II-IV colorectal cancer using a nano-based detection method.

Background: Colorectal cancer (CRC) is a leading cause of cancer mortality globally, underscoring the urgency for a noninvasive and effective biomarker to enhance patient prognosis. Circulating tumor cells (CTCs), a potential marker for real-time tumor monitoring, are limited in clinical utility due to the low sensitivity of existing detection methods. Previously, we introduced a novel nano-based CTCs detection method that relies on the electrical properties of cell surfaces, thus eliminating the need for specific molecular biomarkers. In this study, we used this technique to evaluate the diagnostic and prognostic value of CTCs in stage II-IV CRC.

Methods: A total of 194 participants were included, consisting of 136 CRC patients and 58 healthy individuals. The peripheral blood of the participants was collected, and CTC enumeration was performed utilizing the nano-based detection method that we newly developed. The receiver operating characteristic (ROC) curve and multivariate Cox proportional-hazards analysis were used to assess the effectiveness of CTCs for diagnosing CRC and predicting patient prognosis.

Results: The nano-based method demonstrated an ability to differentiate CRC patients from healthy individuals with a sensitivity of 84.6% and a specificity of 94.8%. Furthermore, baseline CTC levels were predictive of progression-free survival (PFS) in CRC patients, with lower levels associated with longer PFS compared to higher levels (4.5 vs 8.0 months at 15 CTCs/mL, p = 0.016; 4.4 vs 8.0 months at 20 CTCs/mL, p = 0.028). We also explored the dynamic changes in the number of CTCs after 1 to 5 cycles of chemotherapy. Patients with increasing CTC levels typically experienced disease progression (PD), while those with decreasing levels often achieved a partial response (PR) or maintained stable disease (SD). These findings suggest that the dynamic fluctuations in CTC counts are closely tied to the clinical course of the disease.

Conclusion: Our study indicates the potential of nano-based CTCs detection in diagnosing and predicting outcomes for patients with stage II-IV CRC.

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