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Evaluation of the Establishment and Application of a Multimodal Molecular Probe Radiomics Model for Mediastinal Lymph Node Metastasis in Lung Cancer: A Prospective Study

Evaluation of the Establishment and Application of a Multimodal Molecular Probe Radiomics Model for Mediastinal Lymph Node Metastasis in Lung Cancer: A Prospective Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600117165
Enrollment
Unknown
Registered
2026-01-20
Start date
2026-01-20
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suspected mediastinal lymph node metastasis in non-small cell lung cancer

Interventions

Gold Standard:Histologically confirmed
Index test:Contrast-enhanced CT, 18F-FDG PET/CT, 18F-FAI PET/CT

Sponsors

jiangxi cancer hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age = 18 years, and clinically highly suspected of primary lung cancer (based on imaging or clinical features). 2. Planned to undergo radical lobectomy or pneumonectomy, with consent for concurrent systematic mediastinal lymph node dissection. 3. Able to complete all three multimodal imaging examinations at the designated study imaging center within the specified preoperative time window (e.g., 2–4 weeks). 4. The patient understands the study purpose, procedures, and potential risks, and has voluntarily provided written informed consent.

Exclusion criteria

Exclusion criteria: 1. Previous treatment for the currently suspected lung cancer (such as needle biopsy, neoadjuvant chemotherapy/radiotherapy, ablation therapy, etc.). 2. Definitive evidence of distant metastasis (Stage IV) or concurrent other active malignant tumors. 3. Clear contraindications to enhanced CT or PET/CT examinations (e.g., severe allergy to contrast agents, pregnancy, severe renal insufficiency that cannot be corrected). 4. Inability to tolerate the planned surgery as assessed due to cardiopulmonary dysfunction or other severe systemic diseases. 5. Poor compliance or data integrity: inability to cooperate with all study procedures or circumstances that may lead to missing critical data (such as imaging or pathological data).

Design outcomes

Primary

MeasureTime frame
Multimodal Molecular Probe Imaging Features;Accuracy;

Secondary

MeasureTime frame
Sensitivity;Specificity;

Countries

China

Contacts

Public ContactJiangYeQing

jiangxi cancer hospital

625185632@qq.com+86 791 8830 0680

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026