Blood test may spot lung cancer mutations faster
NCT ID NCT04912687
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at whether a simple blood test (liquid biopsy) can detect EGFR gene mutations in people with advanced non-small cell lung cancer. Researchers collected blood samples from 581 patients and compared the results with standard tissue testing. The goal was to see if adding the blood test helps find more patients who could benefit from targeted therapy.
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 approach could make it easier and faster to detect treatable genetic mutations in lung cancer, helping doctors choose the right treatment sooner.
- What could go wrong
- This is an observational study, not a treatment trial. It only tests a diagnostic method, so it won't directly improve outcomes. The blood test may miss some mutations found in tissue.
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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581 people
The number who actually took part.
- Started
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Jan 2022
- Finished
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Jan 2026
- 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. Male or female patients aged ≥ 18 years at time of proposal study, 2. Histologically confirmed non-small cell lung carcinoma, 3. No previous treatment for NSCLC, 4. Indication to EGFR status determination following HAS recommendation, 5. Voluntary signed and dated written informed consent prior to any study specific procedure 6. Patients with a social security in compliance with the French Law. Exclusion Criteria: 1. Treatment for advanced NSCLC started before liquid biopsy sampling. 2. Involvement in the planning and/or conduct of the study (applies to both Investigator staff and/or staff at the study site).
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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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CHRU Lille
Lille, 59037, France
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CHU Nice-Hopital de Cimiel
Nice, 06000, France
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CHU Poitiers
Poitiers, 86021, France
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CHU Strasbourg
Strasbourg, 67091, France
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CHU de Rennes - Hopital Pontchaillou
Rennes, 35033, France
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Hospices Civils de Lyon
Lyon, 69002, France
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Institut Bergonie
Bordeaux, 33076, France
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Institut Curie
Paris, 75248, France
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Institut de Cancérologie de l'Ouest - Site Paul Papin
Angers, 49000, France
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