AI reads scans and genes to predict lung cancer drug success
NCT ID NCT07287904
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study uses artificial intelligence to analyze CT scans, pathology slides, and genetic reports from 1,000 lung cancer patients with EGFR mutations. The goal is to build a model that predicts how well targeted therapy will work after surgery. If successful, it could help doctors choose the best treatment for each patient.
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 AI model could help doctors better predict which lung cancer patients will benefit most from targeted therapy, leading to more personalized treatment.
- What could go wrong
- This is a retrospective study, meaning it looks back at past data, not a prospective trial. The AI model may not work as well in real-world settings or on new patients.
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.
- Participants
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About 1,000 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2025
An estimate. Start dates often move.
- Expected to finish
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Aug 2027
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.
Who is studied
Retrospectively included data from 1000 patients diagnosed with stage IB-IIIA invasive lung adenocarcinoma with EGFR mutations who underwent radical surgery from January 2021 to December 2024.
- Ages
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18 to 80 years
- 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: 1. Age 18-80 years, undergoing radical surgery for lung cancer (R0 resection); 2. Postoperative pathological stage IB-IIIA, pathology confirmed as adenocarcinoma; 3. EGFR gene testing positive, EGFR 19del/L858R mutation; 4. Receiving postoperative EGFR-TKI targeted adjuvant therapy; 5. Complete and clear preoperative imaging data, genetic testing report, and pathology report available. Exclusion Criteria: 1. Patients negative for EGFR; 2. Incomplete surgical resection (R1, R2); 3. Did not receive EGFR-TKI targeted therapy after surgery; 4. Recurrent or advanced stage patients; 5. Incomplete preoperative or postoperative data; 6. Patients who died within 30 days post-surgery.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Wuhan Union Hospital
Wuhan, Hubei, 430022, China
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Other studies related to the condition(s) this trial covers.
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