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NCT Number: NCT07110259

AI-Based DeepGEM Tool for Predicting Gene Mutations in NSCLC Patients: A Randomized Controlled Study

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).

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age between 18 and 75 years, inclusive, at the time of enrollment.
  • Histologically or cytologically confirmed non-small cell lung cancer (NSCLC) with clinical stage II-IV as per the 8th edition of the AJCC staging system.
  • Availability of qualified histopathological whole-slide images that can be reviewed through the KindMED system(DeepGEM).
  • Successful mutation prediction of EGFR, ALK, or ROS1 by the DeepGEM AI tool.
  • No prior systemic anti-cancer therapy, including chemotherapy, targeted therapy, or immunotherapy.
  • Willing and able to comply with study requirements, including follow-up and treatment; written informed consent must be provided.

Exclusion criteria

  • Prior systemic anti-tumor therapy (chemotherapy, radiotherapy, targeted therapy-including but not limited to monoclonal antibodies or tyrosine kinase inhibitors) before enrollment.
  • Failure of DeepGEM analysis or unqualified histopathological image quality.
  • History of any other malignancy within the past 5 years, except for adequately treated basal cell carcinoma of the skin or in situ carcinoma (e.g., cervical carcinoma in situ).
  • Cognitive or psychological barriers to understanding or accepting AI-based prediction or molecular testing.
  • Pregnant or breastfeeding women, or women of childbearing potential who are not using effective contraception.
  • Any other clinical condition that, in the opinion of the investigators, may interfere with the study protocol or compromise participant safety, including poor compliance with study procedures.

Treatment and study plan

DeepGEM-guided Molecular Testing and Treatment

Other

Artificial intelligence-based mutation prediction using DeepGEM to guide clinical decision-making for molecular testing and therapy selection.

Standard Diagnostic Pathway

Other

DeepGEM is used for eligibility screening, but its results are withheld. Clinicians manage patients per standard diagnostic and treatment practices.

Primary outcomes

  1. Overall Survival (OS)

    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.

  2. Targeted Therapy Utilization Rate

    Time frame: Up to 6 months post-randomization

    Proportion of participants receiving molecularly matched targeted therapies based on standard genetic testing.

Secondary outcomes

  1. Molecular Testing Rate

    Time frame: Up to 3 months

    Proportion of participants who undergo molecular testing after initial DeepGEM prediction.

  2. Prediction Concordance

    Time frame: Up to 3 months

    Concordance between DeepGEM-predicted mutation status and results from PCR or NGS molecular testing.

  3. Cost-effectiveness of DeepGEM

    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.

Study contacts

Contact information is provided by the study sponsor or research team.

Jianxing He, PhD

CONTACT

[email protected]

13802777270

Wenhua Liang, PhD

CONTACT

[email protected]

13710249454

Sponsors and collaborators

Lead sponsor

Jianxing He

Other

Collaborators

  • Guangzhou Kingmed Diagnostics Co., Ltd.

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
Aug 7, 2025
Registry last updated
Aug 7, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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.