Study on Early Auxiliary Diagnosis and Postoperative Recurrence Monitoring of Breast Cancer

Sponsor
Singlera Genomics Inc. (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05858242
Collaborator
Beijing Friendship Hospital (Other)
100
1
35.8
2.8

Study Details

Study Description

Brief Summary

This study screened and identified effective methylation markers in breast cancer, established a detection system for early screening and early diagnosis, and provided a research basis for the embryonic form of non-invasive breast cancer early screening products in later incubation. Then, the plasma ctDNA polygene methylation test was performed for early and middle stage breast cancer patients who were to receive radical surgery for initial treatment, and the predictive effect of postoperative plasma ctDNA methylation status on postoperative prognosis of breast cancer was discussed. In addition, the application value of dynamic monitoring of ctDNA methylation in plasma for postoperative recurrence risk monitoring was explored through regular postoperative follow-up of stage I-III breast cancer patients undergoing radical surgery.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    1. This study will be divided into two stages. The first stage will complete the screening, identification, model construction and target verification of polygene methylation markers in the blood of breast cancer patients. The second stage will explore its application in monitoring prognosis and recurrence after radical mastectomy.

    2. The first stage (inclusion detection period) : By detecting the DNA methylation characteristics of breast cancer (including tissue and plasma) and non-breast cancer samples (breast tissue/plasma of healthy people, and plasma samples of patients with benign breast lesions), screening, identification and verification of plasma ctDNA polygene methylation markers that can distinguish the differences between breast cancer and non-breast cancer samples are carried out.

    3. The second stage (postoperative monitoring and evaluation) : The enrolled group was the initially treated patients who planned to undergo radical mastectomy. Plasma methylation markers were detected before surgery at baseline, and dynamic monitoring of plasma ctDNA polygene methylation detection, related tumor markers and imaging examinations were performed 3 weeks after surgery (or before the start of chemotherapy) and regular follow-up review (once every 3 months for 2 years). To explore the clinical application value of ctDNA methylation status in postoperative breast cancer surgery and follow-up monitoring.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    100 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Early Auxiliary Diagnosis and Postoperative Recurrence Monitoring of Breast Cancer Based on Plasma ctDNA Methylation Markers
    Actual Study Start Date :
    Mar 7, 2023
    Anticipated Primary Completion Date :
    Mar 1, 2026
    Anticipated Study Completion Date :
    Mar 1, 2026

    Arms and Interventions

    Arm Intervention/Treatment
    Early and mid-stage breast cancer patients awaiting radical surgery

    To explore the predictive effect of plasma ctDNA methylation on postoperative prognosis of breast cancer and the application value of monitoring postoperative recurrence risk through regular postoperative follow-up of stage I-III breast cancer patients undergoing radical surgery.

    Outcome Measures

    Primary Outcome Measures

    1. Finding the characteristic ctDNA methylation targets of breast cancer [assessed up to 36 months]

      Establish and verify the early screening model of breast cancer, evaluate the specificity and sensitivity of the model.

    2. To explore the application of postoperative ctDNA methylation in the evaluation of the curative effect of breast cancer surgery and follow-up monitoring [assessed up to 36 months]

      The positive and negative prediction rates of ctDNA methylation markers in plasma were analyzed for the recurrence rate 2 years after radical mastectomy for stage I-III breast cancer.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes

    The first stage Inclusion Criteria:

    Women between the ages of 18 and 80 who are not pregnant or lactating; Meet any of the following categories:

    1. Breast cancer Newly diagnosed breast cancer patients [according to breast cancer TNM staging]; The patient was not accepted prior to blood collection Any breast cancer antitumor related treatment, including surgery, transplantation, radiation, chemotherapy, etc.

    2. precancerous lesions Dysplasia, carcinoma in situ, atypical hyperplasia, etc., no previous history of malignant tumor.

    3. Benign lesions These include fibroadenoma of the breast, intraductal papilloma of the breast, cystic hyperplasia of the breast, lobulated tumors of the breast, Plasma cell mastitis.

    4. Healthy people No abnormal breast, no history of malignancy within 5 years; Age 50 years or above.

    Exclusion Criteria:
    1. previous breast cancer;

    2. A history of other cancers;

    3. Patients who have received major surgical treatment such as blood transfusion or transplantation within 3 months

    4. Participate in other interventional clinical researchers, pregnant or lactating women, or patients suffering from autoimmune diseases, genetic diseases, mental disorders, etc., within 3 months.

    5. Patients with other diseases deemed unsuitable for inclusion by the researcher;

    The second stage Inclusion Criteria:

    1. Patients with definite pathological diagnosis of breast cancer who were to receive radical surgery after preoperative evaluation for initial treatment

    2. Women aged between 18 and 80 who are not pregnant or lactating;

    3. The radical surgery to be received includes mastectomy radical surgery, simple excision + sentinel lymph node biopsy and modified radical surgery, and on this basis, mastectomy plastic surgery, stage I reconstruction and other operations that have the same radical treatment effect and do not affect the entire standardized treatment of patients

    4. Enrolled patients were newly treated breast cancer patients without prior malignant tumor history and treatment history

    Exclusion Criteria:
    1. Stage IV breast cancer patients, or ECOG score > 2.

    2. A history of malignant tumor or other hereditary diseases;

    3. Have received organ transplantation, stem cell transplantation, bone marrow transplantation or received blood transfusion within the past month;

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Beijing Friendship Hospital Affiliated to Capital Medical University Beijing Beijing China 100050

    Sponsors and Collaborators

    • Singlera Genomics Inc.
    • Beijing Friendship Hospital

    Investigators

    • Principal Investigator: Liu Rui, Doctor, Singlera Genomics Inc.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Singlera Genomics Inc.
    ClinicalTrials.gov Identifier:
    NCT05858242
    Other Study ID Numbers:
    • KYS-2022002
    First Posted:
    May 15, 2023
    Last Update Posted:
    May 15, 2023
    Last Verified:
    Feb 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Singlera Genomics Inc.
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 15, 2023