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  • MRD postoperative recurrence monitoring platform

    Minimal Residual Disease, abbreviated as MRD, refers to small residual lesions,

    It refers to the small amount of cancer cells remaining in the body after cancer treatment,

    Measurable Residual Disease (MRD) can also be used to measure residual lesions;

    Molecular residual disease (MRD), also known as molecular residual lesion, can be used in solid tumors.

    Multiomics mMRD360 postoperative patient recurrence monitoring

    Minimal residual disease, abbreviated as MRD, refers to a small amount of cancer cells remaining in the body after cancer treatment. Measurable residual disease (MRD) can also be used to measure residual lesions; Molecular residual disease (MRD), also known as molecular residual lesion, can be used in solid tumors. The evaluation of minimal residual lesions (MRD) can effectively indicate the healing status of colorectal cancer patients after treatment.

    Premed has developed MRD products such as colon cancer, lung cancer, bladder cancer, stomach cancer and breast cancer based on cfDNA methylation, ctDNA and serum tumor markers.

    MRD characteristics (MRD detection runs through the full cycle management of cancer patients):

    1) After curative treatment, determine metastasis or recurrence;

    2) Evaluate the effect through quantitative monitoring before and after treatment;

    3) Choose an effective treatment plan.

    4) CtDNA MRD can be used as a prognostic stratification and recurrence monitoring indicator in various solid tumors, and its detection effect is superior to traditional clinical or imaging methods, with disease traces detected 3 to 12 months in advance of clinical symptoms or imaging.[1]

    [1]Coakley M, Garcia-Murillas I, Turner NC. Molecular Residual Disease and Adjuvant Trial Design in Solid Tumors.Clin Cancer Res. 2019 Oct 

    Technical comparison

    Premed multiple targetsMRD (mMRD)

    NGS-based MRD(nMRD)

    Target/target coverage

    Two methylation+5-7 point mutation+2-3 serum protein combinations/multiple gene and multi-level targets such as lung cancer effectively improve the coverage of recurrence detection, cover the internationally recognized mainstream targets for cancer and lung cancer, and cover 90% of NGS

    Covering sites with more low-frequency mutations

    Cost performance

    High cost-effectiveness of multiple postoperative monitoring under the same monitoring indicators (in the thousands of yuan level)

    Low cost-effectiveness of multiple postoperative monitoring under the same monitoring indicators (at the level of 10000 yuan)

    Reporting period

    1days

    7 days

    Coincidence rate

    70%-80%

    The coincidence rate of the first postoperative detection of NGS MRD in Guardian Reveal colon cancer by Guardian Heath in the United States is 50%

    Registration Certificate

    Most have obtained NMPA registration certificates and there are fees

    Unable to apply for registration certificate

    Multiple omics protocols for colorectal cancer MRD:

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    Early detection of malignant mutations in small pulmonary nodules, special MRD testing for lung cancer patients

    Overview of Lung Cancer

    Lung cancer is the highest incidence of cancer in China, and its incidence rate and mortality rate are the first. 787000 new cases of lung cancer accounted for 20.03% of the total new cases. 631000 lung cancer deaths accounted for 26.99% of the total deaths. According to the degree of differentiation, morphological characteristics, and biological characteristics of lung cancer, it is currently divided into two major categories, namely small cell lung cancer and non-small cell lung cancer, which include squamous cell carcinoma, adenocarcinoma, large cell carcinoma, etc.

    The pathogenesis of lung cancer is not yet fully understood, but there is evidence that the occurrence of lung cancer is related to factors such as smoking, air pollution, occupational carcinogens, diet, genetics, etc. Overall, both genetic and environmental factors are involved in its onset.


    The relationship between pulmonary nodules and lung cancer

    Pulmonary nodules refer to solitary, well-defined nodules with a diameter of less than or equal to 3cm and surrounded by aerated lung tissue. A pulmonary nodule with a diameter less than or equal to 1cm is called a pulmonary nodule. The common causes of pulmonary nodules are tumors, infectious granulomas, congenital lesions, etc. There are cancerous nodules less than 8mm, and benign nodules greater than 8mm. Some patients with early lung cancer present as pulmonary nodules. Tracking studies have shown that a small nodule can gradually become cancer after ten to twenty years. Once a pulmonary nodule is discovered, regular follow-up is recommended. Due to the clear correlation between tumor size and staging and prognosis, rapid identification of benign and malignant lung nodules, removal of malignant lesions, avoidance of unnecessary benign lesion resection, and reduction of patient economic burden are currently hot topics in the diagnosis and treatment of lung cancer.


    Clinical significance of lung cancer MRD detection

    Minimal residual disease (MRD) refers to a small amount of cancer cells remaining in the body after cancer treatment, which cannot be detected by traditional imaging (including PET/CT) or laboratory methods. However, MRD releases circulating cell free tumor DNA (ctDNA). Therefore, based on the ctDNA/cfDNA methylation and other omics panels, the application of liquid biopsy technology [1] can track MRD. Detection and tracking of MRD can more accurately support cancer treatment decisions compared to traditional clinical or imaging methods. By identifying abnormal molecules from cancer sources, predicting the persistence and clinical progression of MRD, the entire process management of postoperative residual, efficacy evaluation, recurrence detection, and metastasis evaluation in cancer patients can be achieved [2] (Figure 1) (Figure 2)




    Recommended inspection time
    Detection cycle Recommended inspection points
    Treatment period Preoperative 1-2 weeks after surgery 1-3 months after surgery
    Follow-up period Once every 3-6 months
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    Multiomics mMRD360
    Postoperative Patient Recurrence Monitoring Platform

  • Hotline: 0512-87662791-8001

  • Address: 3rd Floor, Building 16, Northwest District, Nano City, No. 99, Jinjihu Avenue, Suzhou Industrial Park

  • Cooperation:

    13761818715

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