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Clinical Trials in China / NCT07287904
Starting soon Observational

Prediction of Targeted Therapy Efficacy in EGFR-mutant Lung Cancer Patients Using AI-based Multimodal Data

NCT07287904 · tracked via the Priya Life Science China tracker
Sponsor
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Phase
Observational
Started
2025-12-25
Last updated
2025-12-17

Condition(s) studied

Lung Cancer (NSCLC)EGFR Activating MutationAdenocarcinoma LungPostoperative Adjuvant Therapy

Investigational drug(s) / intervention(s)

Comprehensive analysis through laboratory tests, imaging techniques, and clinical data

Comprehensive analysis through laboratory tests, imaging techniques, and clinical data: Extract radiomics features of the tumor and peritumoral regions from preoperative CT images, H\&E-stained digital pathology whole-slide images, and genetic test reports, and integrate them with multidimensional pathological features and gene expression distribution characteristics to construct a radiopathogenomic multi-omics modality, providing more precise prognostic assessment for targeted therapy in lung cancer patients.

Study summary

The main purpose of this study is to explore the value of multimodal imaging information and models in predicting the prognosis of EGFR-positive non-small cell lung cancer patients undergoing targeted therapy, providing a basis for selecting suitable populations for precise tumor treatment and corresponding therapy. We retrospectively analyzed patient case data, extracted preoperative CT images, H\&E-stained whole-slide digital pathology images, and pre- or postoperative genetic testing reports to extract radiomic features of tumor and peritumoral regions. These features were combined with multidimensional pathological features and gene expression distribution characteristics to construct a multimodal radiopathogenomic model, offering more precise prognostic evaluation for lung cancer patients receiving targeted therapy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Wuhan Union Hospital Wuhan Hubei

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07287904 on ClinicalTrials.gov ↗ ← All trials in China