Non-Invasive Malignancy Classifiers Using Blood-Biomarkers for Lung Nodule Evaluation (NIMBLE)
NIMBLE | Non-Invasive Malignancy Classifiers Using Blood-Biomarkers for Lung Nodule Evaluation
The goal of the NIMBLE study is to evaluate blood-based biomarkers for lung cancer risk prediction in patients referred with a lung nodule.
Each blood biomarker will be evaluated for descriminating malignant from benign lung nodules alone and in combination with other blood biomarkers, patient characteristics and radiological features.
研究概览
详细说明
Lung nodules are frequent findings on chest CT scans. The majority of nodules are benign, but a substantial fraction will be malignant. The decision to pursue invasive diagnostics currently rely on a risk estimate based on patient characteristics and radiological features of the nodule.
Accurate risk estimation is crucial as invasive diagnostics comes with a significant risk of severe complications such as collapsed lung, bleeding, infections and in rare cases death. The NIMBLE project seeks to improve the early risk assessment by incorporation of blood biomarkers in the risk algorithm. The study will include 1,200 patients with a nodule when patients are referred to the dept. of pulmonology and perform an addition blood draw. The blood will be analyzed using a wide range of blood tests. These will include standard blood tests, novel protein tumor markers specifically targeting lung cancer, an epigenetic smoking marker (AHRR methylation), and combined fragmentome, mutational and methylome analysis of cell-free tumor DNA.
Blood tests will be evaluated following REMARK guidelines in terms of lung cancer predictive performance but also in terms of feasibility in implementation in daily routine testing at a Dept. of Clinical Biochemistry.
The study will perform all tests on patient material collected at baseline when patients are referred to work-up and use machine learning to optimally combine blood tests with patient characteristics and radiological features.
研究类型
注册 (估计的)
联系人和位置
学习联系方式
- 姓名:Søren Egstrand, MD, PhD
- 电话号码:0045 21682147
- 邮箱:soeren.egstrand@regionh.dk
学习地点
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Gentofte Municipality、丹麦
- 招聘中
- Gentofte Hospital
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接触:
- Søren Egstrand, MD, PhD
- 电话号码:0045 21682147
- 邮箱:soeren.egstrand@regionh.dk
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参与标准
资格标准
适合学习的年龄
- 孩子
- 成人
- 年长者
接受健康志愿者
取样方法
研究人群
描述
Inclusion Criteria:
- Patients with a newly detected IPN suspected of lung cancer referred to the infiltrate unit
- Having signed informed consent
Exclusion Criteria:
- Active cancer, excluding non-melanoma skin cancer
- Comorbidities that exclude the patient from clinical follow-up and final diagnosis
学习计划
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
干预/治疗 |
|---|---|
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Patients referred for work-up suspected of lung cancer
Patients are enrolled when these are referred to the Pulmonology Department suspected of lung cancer.
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Standard blood tests, Novel protein tumor markers specifically targeting lung cancer, Epigenetic smoking marker (AHRR methylation), Combined fragmentome, mutational and methylome analysis of cell-free tumor DNA
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
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Lung cancer diagnosis during work-up
大体时间:At least two years of followup
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At least two years of followup
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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