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NCT Number: NCT06001528

Serum and Tissue Metabolite-based Prediction of Sentinel Lymph Node Metastasis in Breast Cancer

Breast cancer is a malignant tumor with the highest morbidity and mortality among women worldwide. Accurate staging of axillary lymph nodes is critical for metastatic assessment and decisions regarding treatment modalities in breast cancer patient. Among patients who underwent sentinel lymph node biopsy, about 70 % of the patients had negative pathological results and in other words, these 70 % of the patients received unnecessary surgery. At present, imaging and pathological diagnosis is the main measure of lymph node metastasis in breast cancer. However, limitations remained. Artificial intelligence, including deep learning and machine learning algorithms, has emerged as a possible technique, which can make a more accuracy prediction through machine-based collection, learning and processing of previous information, especially in radiology and pathology-based diagnosis. With the intensification of the concept of precision medicine and the development of non-invasive technology, the investigators intend to use the artificial intelligence technology to develop a serum and tissue-based predictive model for sentinel lymph node metastasis diagnosis combined with imaging and pathological information, providing specific, efficient and non-invasive biological indicators for the monitoring and early intervention of lymph node metastasis in patient with breast cancer. Therefore, the investigators retrospectively include serum samples from early breast cancer patients undergoing sentinel lymph node biopsy, including a discovery cohort and a modeling cohort. Metabolites were detected and screened in the discovery cohort and then as the target metabolites for targeted detection in the modeling cohort. Combined with preoperative imaging and pathological information, a prediction model of breast cancer sentinel lymph node metastasis based on serum metabolites would be established. Subsequently, multi-center breast cancer patients will prospectively be included to verify the accuracy and stability of the model.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Shantou Central Hospital

Shantou, Guangdong, China

Location status: Recruiting

Location contact

Xiaorong Lin, Dr.

CONTACT

[email protected]

13790891600

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Pathological diagnosis of breast cancer
  • No preoperative therapy including chemotherapy or endocrine therapy
  • No distant metastasis
  • Underwent mastectomy or breast-conserving surgery with sentinel lymph node biopsy
  • Agreed to provide preoperative peripheral blood samples
  • Had access to imaging, pathological and follow-up data for preoperative and postoperative evaluation of the disease

Exclusion criteria

  • Neoadjuvant therapy
  • Presence of distant metastasis at time of diagnosis
  • Primary malignancies other than breast cancer
  • Bilateral breast cancer or previous contralateral breast cancer
  • Undergo modified radical surgery for breast cancer without sentinel lymph node biopsy
  • Incomplete pathological data and follow-up data
  • Pregnancy and other conditions determined by the investigator to be ineligible for inclusion in the study

Treatment and study plan

Primary outcomes

  1. Metabolic difference detection

    Time frame: From January 01, 2021 to December 31, 2021

    Serum metabolites difference between breast cancer patients with and without sentinel lymph node metastasis would be analyzed, and potential biological indicators found.

  2. Predictive model establishment

    Time frame: From January 01, 2022 to December 31, 2022

    Combined with preoperative imaging and pathological information, a predictive model of sentinel lymph node metastasis in breast cancer would be established based on the metabolic difference.

  3. Predictive model validation

    Time frame: From January 01, 2023 to December 31, 2023

    Verify the stability and accuracy of our model in larger cohorts and promote clinical translation.

Study contacts

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

Xiaorong Lin, Dr.

CONTACT

[email protected]

13790891600

Sponsors and collaborators

Lead sponsor

Shantou Central Hospital

Other

Collaborators

  • Shenshan Medical Center of Sun Yat-sen Memorial Hospital
  • Sichuan Cancer Hospital and Research Institute
  • Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
  • Zhejiang Cancer Hospital

Registry information

Important dates

Study start
2021
Primary completion
2023
Study completion
2026
First posted
Aug 21, 2023
Registry last updated
Sep 28, 2023

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.

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