Seeing the immune battle inside lung tumors: a new imaging tracer under the microscope
NCT ID NCT05157659
First seen Aug 20, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This study tests a new PET imaging tracer called [18F]F-AraG to see if it can spot activated T-cells inside non-small cell lung cancer tumors. Researchers will scan about 10 patients with resectable lung cancer, then compare the tracer's uptake with lab analysis of the removed tumor tissue. The goal is to understand how well this tracer works for imaging immune activity, which could eventually help tailor treatments.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A PET scan using the experimental tracer [18F]F-AraG to visualize activated T-cells in tumors.
- What this could lead to
- If successful, this imaging method could help doctors see how active the immune system is inside tumors, potentially guiding immunotherapy decisions.
- What could go wrong
- This is a small early imaging study, so the tracer may not reliably reflect T-cell activity, and results may not translate to routine clinical use.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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 10 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2021
- Expected to finish
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Dec 2026
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 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Histologically confirmed NSCLC, a histological biopsy is mandatory. 2. Patients that are resectable upfront as per multidisciplinary tumor board evaluation. 3. Be willing and able to provide written informed consent for the trial. 4. Be above 18 years of age on day of signing informed consent. 5. Have a performance status of 0-1 on the ECOG Performance Scale at screening. Exclusion Criteria: 1. Subjects with a condition requiring systemic treatment with either corticosteroids (\> 10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of screening. Inhaled or topical steroids, and adrenal replacement steroid \>10 mg daily prednisone equivalent, are permitted in the absence of active autoimmune disease. 2. Psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial. 3. Patient is pregnant or breastfeeding or expecting to conceive within the projected duration of the trial, starting with the screening visit through 12 weeks after the last \[18F\]F-AraG PET scan.
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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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Amsterdam UMC, location VU University Medical Center
Amsterdam, Nederland, 1081HV, Netherlands
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Other studies related to the condition(s) this trial covers.
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