CYFRA 21-1、CA 125和CEA在首次CT扫描时为疾病稳定的NSCLC患者提供了额外的预后价值。

Q3 Biochemistry, Genetics and Molecular Biology Tumor Biology Pub Date : 2024-01-01 DOI:10.3233/TUB-220042
Thomas Muley, Mark A Schneider, Michael Meister, Michael Thomas, Claus Peter Heußel, Mark Kriegsmann, Stefan Holdenrieder, Birgit Wehnl, Vinzent Rolny, Anika Mang, Rebecca Gerber, Felix Herth
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引用次数: 0

摘要

背景:血清肿瘤标志物(STM)可以补充成像,并为癌症(NSCLC)患者提供额外的临床信息。目的:确定STM是否可以预测稳定期疾病(SD)患者初次治疗后的预后。方法:这项单中心、前瞻性、观察性试验招募了395名接受III/IV期治疗的幼稚NSCLC患者;其中263名患者被纳入本分析。在初始治疗前后进行计算机断层扫描(CT)并测量STM(两个周期的化疗和/或免疫检查点抑制剂或酪氨酸激酶抑制剂);分析基于在第2周期后第一次CT时获得的CT和STM测量,仅通过Kaplan-Meier曲线和Cox比例风险模型分析PFS和OS。结果:SD(n = 100)根据CYFRA 21-1、CEA和CA 125的测量结果,使用优化的截止值将其分为高风险组和低风险组,估计高风险和低风险SD患者的进展或死亡风险增加了4倍(PFS,HR 4.17;OS,3.99;两者均为p 结论:STM可以为CT反应不确定的患者提供进一步的指导,将他们分为未来PFS和OS事件的高风险组和低风险组。
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CYFRA 21-1, CA 125 and CEA provide additional prognostic value in NSCLC patients with stable disease at first CT scan.

Background: Serum tumor markers (STM) may complement imaging and provide additional clinical information for patients with non-small cell lung cancer (NSCLC).

Objective: To determine whether STMs can predict outcomes in patients with stable disease (SD) after initial treatment.

Methods: This single-center, prospective, observational trial enrolled 395 patients with stage III/IV treatment-naïve NSCLC; of which 263 patients were included in this analysis. Computed Tomography (CT) scans were performed and STMs measured before and after initial treatment (two cycles of chemotherapy and/or an immune checkpoint inhibitor or tyrosine kinase inhibitor); analyses were based on CT and STM measurements obtained at first CT performed after cycle 2 only PFS and OS were analyzed by Kaplan-Meier curves and Cox-proportional hazard models.

Results: When patients with SD (n = 100) were split into high- and low-risk groups based on CYFRA 21-1, CEA and CA 125 measurements using an optimized cut-off, a 4-fold increase risk of progression or death was estimated for high- vs low-risk SD patients (PFS, HR 4.17; OS, 3.99; both p < 0.0001). Outcomes were similar between patients with high-risk SD or progressive disease (n = 35) (OS, HR 1.17) and between patients with low-risk SD or partial response (n = 128) (PFS, HR 0.98; OS, 1.14).

Conclusions: STMs can provide further guidance in patients with indeterminate CT responses by separating them into high- and low-risk groups for future PFS and OS events.

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来源期刊
Tumor Biology
Tumor Biology 医学-肿瘤学
CiteScore
5.40
自引率
0.00%
发文量
18
审稿时长
1 months
期刊介绍: Tumor Biology is a peer reviewed, international journal providing an open access forum for experimental and clinical cancer research. Tumor Biology covers all aspects of tumor markers, molecular biomarkers, tumor targeting, and mechanisms of tumor development and progression. Specific topics of interest include, but are not limited to: Pathway analyses, Non-coding RNAs, Circulating tumor cells, Liquid biopsies, Exosomes, Epigenetics, Cancer stem cells, Tumor immunology and immunotherapy, Tumor microenvironment, Targeted therapies, Therapy resistance Cancer genetics, Cancer risk screening. Studies in other areas of basic, clinical and translational cancer research are also considered in order to promote connections and discoveries across different disciplines. The journal publishes original articles, reviews, commentaries and guidelines on tumor marker use. All submissions are subject to rigorous peer review and are selected on the basis of whether the research is sound and deserves publication. Tumor Biology is the Official Journal of the International Society of Oncology and BioMarkers (ISOBM).
期刊最新文献
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