Simple blood test may reveal early if lung cancer therapy works
NCT ID NCT03926260
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at 100 people with advanced non-small cell lung cancer to see if changes in tumor DNA in the blood (ctDNA) can predict how well treatment is working. Researchers took blood samples before treatment, at 3 weeks, and at 9 weeks. The goal was to see if a rise or fall in ctDNA levels matches tumor shrinkage or growth on scans. This is an observational pilot study, not a test of a new drug.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a simple blood test to quickly tell if lung cancer treatment is working, helping doctors adjust therapy earlier.
- What could go wrong
- This is a small, early pilot study (100 people) that only observes DNA changes—it does not test a new treatment. The findings may not apply to all patients or lead to a reliable test.
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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100 people
The number who actually took part.
- Started
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Jun 2019
- Finished
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May 2022
- 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.
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.
Inclusion Criteria: * Metastatic or locally advanced non-small cell lung cancer (stage III or IV) * At least one measurable target according to RECIST criteria * Identification of at least one molecular alteration in the tissue sample analyzed in the framework of patient management * Performance Status 0 to 2 * Affiliated to a social security system * Patient who can be followed under the protocol * Patient agreed to participate in the study and gave his/her express consent Exclusion Criteria: * Minor * Small cell or mixed bronchial cancer * Radiotherapy (except radiotherapy for antalgic purposes) during the last 7 days * Patient who has already started a first line of treatment * Patient already included in an interventional research protocol that may have an impact on the results of the ELUCID study * History of cancer (with the exception of non-melanoma skin, cervical cancer in situ, adequately treated) with sign of illness during the last 5 years * Patient which, does present a substantial risk of recurrence. * Major under guardianship, curators or deprived of liberty * Pregnant or lactating woman, or of childbearing age without effective contraception * Not affiliated to a social security system * Inability to understand the protocol and / or to give express consent
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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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Jaafar BENNOUNA
Nantes, 44000, France
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Marie MARCQ
La Roche-sur-Yon, 85000, France
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Other studies related to the condition(s) this trial covers.
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