DeepGEM-guided Molecular Testing and Treatment
OtherArtificial intelligence-based mutation prediction using DeepGEM to guide clinical decision-making for molecular testing and therapy selection.
NCT Number: NCT07110259
This prospective, multicenter, randomized controlled trial aims to evaluate the clinical utility of DeepGEM, an artificial intelligence (AI)-based mutation prediction tool based on histopathological whole-slide images, in patients with non-small cell lung cancer (NSCLC). The study will assess whether DeepGEM can facilitate molecular testing, increase targeted therapy utilization, and improve survival outcomes in a real-world clinical setting. Patients with stage II-IV treatment-naïve NSCLC and qualified pathology slides for DeepGEM analysis will be enrolled. Eligible participants with AI-predicted EGFR, ALK, or ROS1 mutations will be randomized in a 4:1 ratio to either the DeepGEM-informed group (clinicians can access AI results to guide further testing and treatment) or the standard care group (clinicians are blinded to AI results and follow routine care).
Trial opening soon.
Get Notified18 year–75 year
All sexes
Interventional
Not applicable
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Artificial intelligence-based mutation prediction using DeepGEM to guide clinical decision-making for molecular testing and therapy selection.
DeepGEM is used for eligibility screening, but its results are withheld. Clinicians manage patients per standard diagnostic and treatment practices.
Time frame: From randomization to death from any cause, assessed up to 36 months
Comparison of OS between the DeepGEM-informed group and the standard care group.
Time frame: Up to 6 months post-randomization
Proportion of participants receiving molecularly matched targeted therapies based on standard genetic testing.
Time frame: Up to 3 months
Proportion of participants who undergo molecular testing after initial DeepGEM prediction.
Time frame: Up to 3 months
Concordance between DeepGEM-predicted mutation status and results from PCR or NGS molecular testing.
Time frame: Up to 12 months
Evaluation of cost per targeted therapy initiated and cost per life-year gained in the DeepGEM group versus standard care.
Contact information is provided by the study sponsor or research team.
Jianxing He, PhD
CONTACT
Wenhua Liang, PhD
CONTACT
Jianxing He
Other
Application of the Artificial Intelligence-Based Gene Mutation Prediction Tool DeepGEM in Patients With Non-Small Cell Lung Cancer (NSCLC): A Prospective, Multicenter, Randomized Controlled Trial
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.