Urinary Metabolite Diagnostic and Prognostic Liquid Biopsy Biomarkers of Lung Cancer in Nonsmokers and Tobacco Smokers.

IF 10 1区 医学 Q1 ONCOLOGY Clinical Cancer Research Pub Date : 2024-08-15 DOI:10.1158/1078-0432.CCR-24-0637
Bhavik Dalal, Takeshi Tada, Daxesh P Patel, Sharon R Pine, Mohammed Khan, Takahiro Oike, Yasuyuki Kanke, Amelia L Parker, Majda Haznadar, Leila Toulabi, Kristopher W Krausz, Ana I Robles, Elise D Bowman, Frank J Gonzalez, Curtis C Harris
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Abstract

Purpose: Nonsmokers account for 10% to 13% of all lung cancer cases in the United States. Etiology is attributed to multiple risk factors including exposure to secondhand smoking, asbestos, environmental pollution, and radon, but these exposures are not within the current eligibility criteria for early lung cancer screening by low-dose CT (LDCT).

Experimental design: Urine samples were collected from two independent cohorts comprising 846 participants (exploratory cohort) and 505 participants (validation cohort). The cancer urinary biomarkers, creatine riboside (CR) and N-acetylneuraminic acid (NANA), were analyzed and quantified using liquid chromatography-mass spectrometry to determine if nonsmoker cases can be distinguished from sex and age-matched controls in comparison with tobacco smoker cases and controls, potentially leading to more precise eligibility criteria for LDCT screening.

Results: Urinary levels of CR and NANA were significantly higher and comparable in nonsmokers and tobacco smoker cases than population controls in both cohorts. Receiver operating characteristic analysis for combined CR and NANA levels in nonsmokers of the exploratory cohort resulted in better predictive performance with the AUC of 0.94, whereas the validation cohort nonsmokers had an AUC of 0.80. Kaplan-Meier survival curves showed that high levels of CR and NANA were associated with increased cancer-specific death in nonsmokers as well as tobacco smoker cases in both cohorts.

Conclusions: Measuring CR and NANA in urine liquid biopsies could identify nonsmokers at high risk for lung cancer as candidates for LDCT screening and warrant prospective studies of these biomarkers.

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非吸烟者和吸烟者肺癌的尿代谢物诊断和预后液体活检生物标记物
目的:在美国,非吸烟者占所有肺癌病例的 10-13%。病因归结于多种风险因素,包括接触二手烟、石棉、环境污染和氡,但这些接触并不在目前通过低剂量计算机断层扫描(LDCT)进行早期肺癌筛查的资格标准之内:实验设计:收集了两个独立队列的尿液样本,包括 846 名参与者(探索队列)和 505 名参与者(验证队列)。采用液相色谱-质谱法对癌症尿液生物标志物肌酸核苷(CR)和N-乙酰神经氨酸(NANA)进行了分析和定量,以确定与吸烟者病例和对照组相比,能否将非吸烟者病例与性别和年龄匹配的对照组区分开来,从而为 LDCT 筛查制定更精确的资格标准:结果:在两个队列中,非吸烟者和烟草吸烟者病例尿液中的 CR 和 NANA 水平均明显高于人群对照组,且具有可比性。对探索队列中非吸烟者的 CR 和 NANA 水平进行接收者操作特征(ROC)分析,结果显示曲线下面积(AUC)为 0.94,而验证队列中非吸烟者的曲线下面积(AUC)为 0.80,具有更好的预测性能。Kaplan-Meier生存曲线显示,在两个队列中,高水平的CR和NANA与非吸烟者和吸烟者癌症特异性死亡的增加有关:结论:测量尿液活检中的CR和NANA可确定肺癌高风险非吸烟者作为LDCT筛查的候选者,因此有必要对这些生物标志物进行前瞻性研究。
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来源期刊
Clinical Cancer Research
Clinical Cancer Research 医学-肿瘤学
CiteScore
20.10
自引率
1.70%
发文量
1207
审稿时长
2.1 months
期刊介绍: Clinical Cancer Research is a journal focusing on groundbreaking research in cancer, specifically in the areas where the laboratory and the clinic intersect. Our primary interest lies in clinical trials that investigate novel treatments, accompanied by research on pharmacology, molecular alterations, and biomarkers that can predict response or resistance to these treatments. Furthermore, we prioritize laboratory and animal studies that explore new drugs and targeted agents with the potential to advance to clinical trials. We also encourage research on targetable mechanisms of cancer development, progression, and metastasis.
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