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单核细胞与淋巴细胞比值增加非小细胞肺癌中循环肿瘤细胞的预后价值:一项前瞻性研究。

Monocytes-to-lymphocytes ratio increases the prognostic value of circulating tumor cells in non-small cell lung cancer: a prospective study.

作者信息

Huangfu Yun, Chang Fangfang, Zhang Fengjuan, Jiao Yanru, Han Lei

机构信息

Department of Clinical Medicine, Henan Medical College, Zhengzhou, China.

Eye Institute, Henan Provincial People's Hospital, Zhengzhou, China.

出版信息

Transl Cancer Res. 2024 Jul 31;13(7):3589-3598. doi: 10.21037/tcr-24-10. Epub 2024 Jul 4.

DOI:10.21037/tcr-24-10
PMID:39145074
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11319958/
Abstract

BACKGROUND

Circulating tumor cells (CTCs) has shown important prognostic value in non-small cell lung cancer (NSCLC). However, the present low sensitivity of CTC capture technology restricts their clinical application. This study aims to explore the feasibility of combining the peripheral blood cell (PBC)-derived inflammation-based score with CTCs to increase the prognostic value of CTCs in NSCLC.

METHODS

Sixty volunteers diagnosed with NSCLC were recruited. CTC count and six inflammation-based scores were examined and the association with progression-free survival (PFS) and overall survival (OS) was explored. The changes in the CTC counts before and after the immunotherapy were observed.

RESULTS

Multivariate analysis showed that CTCs >7 [hazard ratio (HR) =9.07; 95% confidence interval (CI): 3.68-22.37, P<0.001] and monocytes-to-lymphocytes ratio (MLR) > 0.2 (HR =3.07; 95% CI: 1.21-7.84; P=0.01) were associated with shorter OS and PFS in patients with NSCLC. Patients with CTCs >7 and MLR >0.2 had 12.30 times increased risk of death (P<0.001) and 6.10 times increased risk of disease progression (P=0.002) compared with those with CTCs ≤7 and MLR ≤0.2. Decreased CTC counts after immunotherapy were closely related to disease control (r=0.535, P=0.01).

CONCLUSIONS

CTCs and MLR are both independent risk factors for prognosis in patients with NSCLC. The combination of CTCs with MLR significantly increased the prognostic value of CTCs, which would contribute to stratification of NSCLC patients and providing precise treatment. Dynamic monitoring of CTCs efficiently shows the immunotherapy response in NSCLC.

摘要

背景

循环肿瘤细胞(CTCs)在非小细胞肺癌(NSCLC)中已显示出重要的预后价值。然而,目前CTCs捕获技术的低敏感性限制了其临床应用。本研究旨在探讨将外周血细胞(PBC)衍生的基于炎症的评分与CTCs相结合,以提高CTCs在NSCLC中的预后价值。

方法

招募60名诊断为NSCLC的志愿者。检测CTCs计数和六个基于炎症的评分,并探讨其与无进展生存期(PFS)和总生存期(OS)的相关性。观察免疫治疗前后CTCs计数的变化。

结果

多因素分析显示,CTCs>7[风险比(HR)=9.07;95%置信区间(CI):3.68-22.37,P<0.001]和单核细胞与淋巴细胞比值(MLR)>0.2(HR=3.07;95%CI:1.21-7.84;P=0.01)与NSCLC患者较短的OS和PFS相关。与CTCs≤7且MLR≤0.2的患者相比,CTCs>7且MLR>0.2的患者死亡风险增加12.30倍(P<0.001),疾病进展风险增加6.10倍(P=0.002)。免疫治疗后CTCs计数的降低与疾病控制密切相关(r=0.535,P=0.01)。

结论

CTCs和MLR均为NSCLC患者预后的独立危险因素。CTCs与MLR的联合显著提高了CTCs的预后价值,这将有助于NSCLC患者的分层并提供精准治疗。对CTCs的动态监测有效地显示了NSCLC中的免疫治疗反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7205/11319958/3775de370698/tcr-13-07-3589-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7205/11319958/7339d403cd20/tcr-13-07-3589-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7205/11319958/3775de370698/tcr-13-07-3589-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7205/11319958/7339d403cd20/tcr-13-07-3589-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7205/11319958/3775de370698/tcr-13-07-3589-f2.jpg

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