Scientists hunt for genetic clues in blood and urine to personalize lung cancer care
NCT ID NCT02597738
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study collects blood, urine, and tissue samples from 330 adults with advanced lung or head and neck cancer to improve precision medicine. Researchers will analyze genetic changes in these samples and grow some tumors in mice to compare DNA. The goal is to refine liquid biopsies and identify biomarkers for better diagnosis and treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 330 people
The number the study aims to enrol. It can still change while the study runs.
- Start date
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Jan 2016
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 99 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Cohort A (Lung/Head and Neck Cancer Group) Inclusion criteria: 1. Unresectable metastatic lung cancer or head and neck cancer or other solid tumor malignancy 2. Current or Former Smokers with greater than or equal to 10 pack year smoking history 3. Candidates for standard or experimental treatment as determined by their treating physician 4. Age 18 years and older 5. Must sign an informed consent approved by the UAMS Institutional Review Board (IRB) Cohort A (Lung/Head and Neck Cancer Group) Exclusion criteria: 1. Any other significant medical or psychiatric conditions which, in the opinion of the enrolling investigator, may interfere with consent or compliance of the treatment regimen 2. Existing diagnosis or evidence of Hepatits C, Rheumatoid Arthritis or any previous solid organ transplant. 3. Existing diagnosis or evidence of organic brain syndrome that might preclude participation in the full protocol 4. Existing diagnosis or history of significant impairment of basal cognitive function that might preclude participation in the full protocol 5. Other significant medical or psychiatric conditions which, in the opinion of the enrolling investigator, may interfere with consent or compliance of the treatment regimen Cohort B (Chronic Inflammatory disease) Inclusion criteria: 1. Chronic inflammatory disease including but not limited to: * Systematic Lupus Erythematosus * Rheumatoid arthritis * Hepatitis C * Ankylosing Sponsylitis * Scleroderma 2. No history of smoking or quit smoking within the last six months 3. Age 18 years and older 4. Must sign an informed consent approved by the UAMS Institutional Review Board (IRB) Cohort B (Chronic inflammatory disease) Exclusion criteria: 1\. Any other significant medical or psychiatric conditions which, in the opinion of the enrolling investigator, may interfere with consent or compliance of the treatment regimen. 2. Existing diagnosis or evidence of organic brain syndrome that might preclude participation in the full protocol. 3\. Existing diagnosis or history of significant impairment of basal cognitive function that might preclude participation in the full protocol. 4\. Other current malignancy(s). Subjects with prior history at any time of any in situ cancer, including lobular carcinoma of the breast in situ, cervical cancer in situ, atypical melanocytic hyperplasia or Clark I melanoma in situ or basal or squamous skin cancer are eligible, provided they are disease-free at the time of registration. Subjects with other malignancies are eligible if they have been continuously disease free for ≥ 5 years prior to the time of registration. 5\. No current steroid treatment or treatment within the last 3 months. Cohort C (At risk for lung cancer) Inclusion criteria: 1. Age 45-74 years 2. Former or current smokers with a 30 or more pack-years of cigarette smoking history 3. Must sign an informed consent approved by the UAMS Institutional Review Board (IRB) Cohort C (At risk for lung cancer) Exclusion criteria: 1. Other current malignancy(s). Subjects with prior history at any time of any in situ cancer, including lobular carcinoma of the breast in situ, cervical cancer in situ, atypical melanocytic hyperplasia or Clark I melanoma in situ or basal or squamous skin cancer are eligible, provided they are disease-free at the time of registration. Subjects with other malignancies are eligible if they have been continuously disease free for ≥ 5 years prior to the time of registration. 2. History of lung cancer 3. History of removal of any portion of the lung, excluding needle biopsy 4. Unexplained weight loss of more than 15 pounds in the 12 months prior to eligibility assessment 5. Recent hemoptysis 6. Pneumonia or acute respiratory infection treated with antibiotics in the 12 weeks prior to eligibility assessment. 7. History of abnormal chest CT examination suspicious for cancer in the 18 months prior to eligibility assessment. 9\. Chronic inflammatory disease including but not limited to: * Systematic Lupus Erythematosus * Rheumatoid arthritis * Hepatitis C * Ankylosing Sponsylitis * Scleroderma Cohort D (healthy people who exercise) Inclusion criteria: 1. Age 18 years and older 2. Must sign an informed consent approved by the UAMS Institutional Review Board (IRB) 3. Must complete and self-report vigorous exercise for 30 minutes Cohort D (healthy people who exercise) Exclusion criteria: 1\. People will be excluded if they have self reported any of the following conditions: diabetes, heart disease, autoimmune disorders or hepatitis. Cohort E (lung cancer with planned resection) Inclusion criteria: 1. Age 18 years and older 2. Must sign an informed consent approved by the UAMS Institutional Review Board (IRB) 3. Lung cancer with planned resection. Cohort E (lung cancer with planned resection) Exclusion criteria: 1. Any other significant medical or psychiatric conditions which, in the opinion of the enrolling investigator, may interfere with consent or compliance of the protocol 2. Existing diagnosis or evidence of Hepatits C, Rheumatoid Arthritis or any previous solid organ transplant. Cohort F (Any solid tumor cancer with radiation therapy) Inclusion criteria: 1. Age 18 years and older 2. Must sign an informed consent approved by the UAMS Institutional Review Board (IRB) 3. Any solid tumor cancer and will receive radiation therapy. Cohort F (Any solid tumor cancer with radiation therapy) Exclusion criteria: 1\. Any other significant medical or psychiatric conditions which, in the opinion of the enrolling investigator, may interfere with consent or compliance of the protocol 3. Existing diagnosis or evidence of Hepatits C, Rheumatoid Arthritis or any previous solid organ transplant.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Arkansas for Medical Sciences
Little Rock, Arkansas, 72205, United States
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Other studies related to the condition(s) this trial covers.
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