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RecruitingNCT07552584BREATHEUpdated Jun 3, 2026

Blood Based Risk Evaluation With AI for Targeted Primary Health Care in Early Lung Cancer Detection

An interventional study of Risk stratification in Lung Cancer (Diagnosis), sponsored by Vejle Hospital. Recruiting at 2 sites in Denmark. Open to participants aged 50 Years and older. Per ClinicalTrials.gov, last updated 2026-06-03.

Sponsored by Vejle Hospital · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
1,000
Allocation
Not applicable
Ages
50 Years and older
Sex
All
01

Study summary

The study is a prospective, non-randomized feasibility study evaluating blood sample and machine learning-based risk stratification for lung cancer in patients with COPD (chronic obstructive pulmonary disease).

Patients with COPD will be recruited in general practice, where they will have a blood sample drawn. All data will be analyzed by the machine learning model, and patients with increased risk of lung cancer will be referred for a low-dose CT scan of the chest.

The primary objective of the study is to evaluate the feasibility of AI and DNA methylation-based risk stratification for lung cancer in patients with COPD in a primary care setting.

The secondary objectives are to evaluate the safety of the risk stratification approach, the potential effects on quality of life and wellbeing, to gain insight into the patient and physician perspectives, and to estimate the health economic consequences.

Read the detailed description

Lung cancer causes the highest number of cancer-related deaths. Around 5000 people are diagnosed with lung cancer annually in Denmark, and people with chronic obstructive pulmonary disease (COPD) have a higher risk compared to the general population. Screening with low-dose computed tomography (LDCT) can reduce the mortality from lung cancer, but patient adherence and LDCT capacity represent considerable challenges.

The selection criteria commonly applied to LDCT screening programs center around age and tobacco consumption resulting in a large number of individuals eligible for screening. A more personalized approach could reduce the resources required for a lung cancer screening program. Smoking is the single greatest risk factor for developing lung cancer, but the damaging effect can vary between individuals. The methylation-level of the AHRR gene was found to be related to the risk of developing lung cancer. Artificial intelligence (AI) is another promising approach to risk evaluation, and a machine learning model based on clinical data and standard blood tests developed by Danish researchers can be used to predict the risk of lung cancer.

The present project aims to investigate the feasibility of blood sample and AI-based risk stratification for lung cancer in patients with COPD treated and followed in general practice.

A thousand patients with COPD will be enrolled by general practitioners located in the general Vejle area in the Region of Southern Denmark. Consenting patients will fill out basic clinical data in an online REDCap database, and then they will have the blood sample collected by a healthcare professional at the general practice clinic. The sample will be transported to the laboratory at Lillebaelt Hospital, Vejle, for analysis.

A collaborative group at Lillebaelt Hospital Vejle will perform the risk stratification including analyzing DNA methylation and running the AI algorithm. Patients with a score indicating increased risk of lung cancer will be referred for LDCT.

The project will evaluate both feasibility, safety, economy and the experiences of the participants and health care professionals.

02

Conditions studied

  • Lung Cancer (Diagnosis)

Keywords

  • Lung cancer
  • Biomarkers
  • Machine learning
  • Risk stratification
  • COPD
03

Who can participate

Ages eligible
50 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Diagnosed with COPD.
  • => 50 years.
  • Former or current smoker.
  • Speaks and understands Danish.
  • Able to give informed consent to participation.

Exclusion criteria

Exclusion Criteria:

  • Had a CT scan of the thorax within 6 months.
  • Received active treatment for cancer within one year (except non-melanoma skin cancer and carcinoma in situ cervicis uteri).
  • Diagnosed with cancer within one year (except non-melanoma skin cancer and carcinoma in situ cervicis uteri).
  • Presents with symptoms giving suspicion of cancer (except non-melanoma skin cancer and carcinoma in situ cervicis uteri).
  • In a condition not allowing diagnostic workup for or treatment of lung cancer.
  • Does not have Eboks (electronic communication with Danish authorities).
04

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
1,000 participants (estimated)

Study arms

  • Experimental
    Risk stratification

    Risk stratification for lung cancer using standard blood tests, machine learning and a DNA methylation analysis.

    Other: Risk stratification

Interventions

  • OtherRisk stratification

    Patients with COPD will have their risk of lung cancer evaluated using a machine learning model incorporating clinical data and standard blood tests as well as a DNA methylation biomarker. If the risk of lung cancer is above the cut-off, the patient will be referred for a low-dose CT scan of the chest. Currently smoking patients will be referred for a smoking cessation program.

05

What researchers measure

Primary outcomes

  1. The fraction of patients consenting to participate in the study.

    The fraction of patients consenting to participate in the study.

    Time frame: 2 years

Secondary outcomes

  1. Number of low-dose CT scans performed

    The total number of low-dose CT scans performed in the study

    Time frame: 2 years

  2. Number of correctly identified lung cancer cases

    The number of correctly identified lung cancer cases when evaluated by the machine learning model, the DNA methylation biomarker, the PLCOm2012 model, and the USPSTF lung cancer screening criteria.

    Time frame: Up to 8 years

  3. Number of lung cancer cases

    The total number of lung cancer cases identified during the study and during 6 years of subsequent follow-up.

    Time frame: Up to 8 years

  4. Stage distribution of lung cancer cases

    The number of lung cancer cases identified within each stage from I-IV.

    Time frame: Up to 8 years

  5. Number of patients with incidental findings on low-dose CT

    The total number of patients with an incidental finding on the low-dose CT scan requiring treatment or further diagnostic procedures.

    Time frame: 2 years

  6. Number of patients without malignant disease who undergo invasive diagnostic procedures

    The number of patients who undergo invasive diagnostic procedures who do not have a lung cancer diagnosis at one and two years of follow-up.

    Time frame: Up to 4 years

  7. Number of adverse events

    The number of adverse events in the form of pneumothorax, bleeding, infection and hospital admission.

    Time frame: 2 years

  8. Number of patients who initiate smoking cessation

    The number and fraction of active smokers initiating and maintaining a smoking cessation program.

    Time frame: Up to 4 years

  9. The fraction of participants who adhere to the study protocol

    The fraction of participants who have the blood sample drawn, and when applicable, the fraction of referred participants who undergo low-dose CT.

    Time frame: 2 years

  10. Differences in World Health Organization Five Well-being Index (WHO-5) score

    Differences in World Health Organization Five Well-being Index (WHO-5) score between patients with and without increased risk of lung cancer after 1 month and 12 months. The scale minimum is 0 and the maximum is 100. A higher score indicates a better outcome.

    Time frame: Up to 3 years

  11. Differences in Anxiety Symptom Scale 2 (ASS-2) score

    Differences in Anxiety Symptom Scale 2 (ASS-2) score between patients with and without increased risk of lung cancer after 1 month and 12 months. The scale minimum is 0 and the maximum is 10. A lower score indicates a better outcome.

    Time frame: Up to 3 years

  12. Differences in Major Depression Inventory 2 (MDI-2) score

    Differences in Major Depression Inventory 2 (MDI-2) score between patients with and without increased risk of lung cancer after 1 month and 12 months. The scale minimum is 0 and the maximum is 10. A lower score indicates a better outcome.

    Time frame: Up to 3 years

  13. Differences in EQ-5D-5L (quality of life) score

    Differences in EQ-5D-5L score between patients with and without increased risk of lung cancer after 1 month and 12 months. Each of the five domains in the scale has a minimum of 1 and the maximum of 5. A lower score indicates a better outcome. The visual analog scale has a minimum of 0 and a maximum of 100. A higher score indicates a better outcome.

    Time frame: Up to 3 years

  14. Health economic consequences

    The estimated health economic consequences of implementing AI and DNA methylation-based risk stratification in a primary healthcare setting including an estimation of the extra workload placed in the primary healthcare sector. A cost-utility analysis will calculate the incremental quality-adjusted life years (QALYs) gained by the program.

    Time frame: Up to 8 years

Other outcomes

  1. Qualitative analysis of interview data

    Selected participants and general practitioner clinics will be invited to participate in interviews. They will inform about their experiences with the study, the intervention, the setting, the logistics and other thoughts, considerations and barriers they might have.

    Time frame: 3 years.

06

Study locations

2 of 2 sites recruiting
  • Lillebaelt Hospital Vejle, University Hospital of Southern Denmark
    Vejle, 7100, Denmark
    Recruiting
  • General practices, Vejle area
    Vejle, Denmark
    • Sara Witting Christensen Wen, MD, PhD · Contact · breathe@rsyd.dk · +45 79409946
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07552584
Lead sponsor
Vejle Hospital
Responsible party
Sponsor
First posted
Apr 27, 2026
Start date
May 26, 2026
Primary completion
Apr 2028 (estimated)
Completion
Apr 2034 (estimated)
Last update
Jun 3, 2026

Study contacts

Sara Witting Christensen WC Wen, MD, PhD
Contact
sara.witting.christensen.wen@rsyd.dk
+45 79406511
Lene Horsted, Study nurse
Contact
breathe@rsyd.dk
+45 79409946
Ole Hilberg, MD, DMSc
study chair · Department of Medicine, Lillebaelt Hospital Vejle, University Hospital of Southern Denmark
Sara Witting Christensen Wen, MD, PhD
principal investigator · Department of Biochemistry and Immunology, Lillebaelt Hospital Vejle, University Hospital of Southern Denmark

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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