Skip to content

Prediction of Lymph Node Metastasis Risk Using Ultrasound Radiomics and Exploration of Its Underlying Mechanisms

Prediction of Lymph Node Metastasis Risk Using Ultrasound Radiomics and Exploration of Its Underlying Mechanisms

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129111
Enrollment
Unknown
Registered
2026-07-31
Start date
2026-07-31
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Breast cancer with axillary lymph node metastasis

Interventions

Gold Standard:Pathological result of lymph node biopsy
Index test:Ultrasound-based radiomics model for predicting lymph node metastasis risk (extracting high-dimensional features including texture, morphology, and intensity distribution from ultrasound im

Sponsors

chongqing university cancer hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years; 2.Clinically or radiologically suspected breast cancer and scheduled to undergo regional lymph node biopsy; 3.Preoperative lymph node ultrasound completed with adequate image quality for radiomics analysis; 4.Residual tissue sample available for research after fulfilling pathological diagnosis requirements; 5.Pathological result clearly defines metastatic or non-metastatic lymph node; 6.Subject voluntarily agrees to participate and signs written informed consent;

Exclusion criteria

Exclusion criteria: 1.Incomplete standardized ultrasound examination or poor image quality that cannot be used for radiomics analysis; 2.Insufficient biopsy sample leaving no residual tissue for research after pathological diagnosis; 3.Pathological result cannot definitively determine lymph node metastasis status; 4.Prior anti-tumor therapy that may affect lymph node metabolic status (e.g., neoadjuvant chemotherapy, targeted therapy, radiotherapy) and considered unsuitable for inclusion by the investigator; 5.Concurrent severe infection, acute exacerbation of metabolic disease, or other conditions that may significantly affect metabolomics results; 6.Incomplete clinical data that cannot meet study analysis requirements; 7.Unwilling to participate in the study or withdrawal of informed consent during the study process;

Design outcomes

Primary

MeasureTime frame
Lymph node metastasis status;Accuracy;

Secondary

MeasureTime frame
Specificity;Sensitivity;

Countries

China

Contacts

Public ContactFang Li

chongqing university cancer hospital

1768308607@qq.com+86 13808312288

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026