[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100652612":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":35,"centralContacts":40,"locations":46,"responsibleParty":65,"collaborators":29,"id":68,"slug":69,"hasResults":70,"nctId":71,"briefTitle":72,"officialTitle":72,"acronym":29,"eligibilityCriteria":73,"healthyVolunteers":74,"sex":75,"minAge":76,"maxAge":29,"enrollmentInfo":77,"targetDuration":29,"studyType":80,"phases":81,"briefSummary":83,"conditions":84,"keywords":29,"overallStatus":49,"whyStopped":29,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":96},{"fullName":5,"class":6},"Sun Yat-sen University","OTHER",[8,14,20],{"label":9,"type":10,"description":11,"interventionNames":12},"MRD-Guided Treatment Discontinuation","EXPERIMENTAL","Patients with dMMR\u002FMSI-H metastatic colorectal cancer who achieve an objective response after 1 year of immunotherapy and have two consecutive negative plasma MRD results will be randomized to discontinue immunotherapy. Patients will enter observation and undergo routine clinical and imaging assessments, with plasma MRD testing every 3 months until the study endpoint.",[13],"Other: Discontinue NA Treatment",{"label":15,"type":16,"description":17,"interventionNames":18},"Continued Immunotherapy","ACTIVE_COMPARATOR","Patients with dMMR\u002FMSI-H metastatic colorectal cancer who achieve an objective response after 1 year of immunotherapy and have two consecutive negative plasma MRD results will be randomized to continue immunotherapy for a total treatment duration of 2 years. Patients will undergo routine clinical and imaging assessments, with plasma MRD testing every 3 months until the study endpoint.",[19],"Other: Continued Immunotherapy",{"label":21,"type":6,"description":22,"interventionNames":23},"Observational Cohort","Patients who achieve disease control for at least 6 months after immunotherapy will undergo plasma MRD testing and prospective follow-up. The study will not interfere with subsequent treatment decisions, including discontinuation or continuation of immunotherapy, surgery, or local treatment. Patients will undergo routine clinical follow-up and serial MRD monitoring according to the study schedule.",[24],"Other: Observation",[26,30,32],{"type":6,"name":27,"description":11,"armGroupLabels":28,"otherNames":29},"Discontinue NA Treatment",[9],null,{"type":6,"name":15,"description":17,"armGroupLabels":31,"otherNames":29},[15],{"type":6,"name":33,"description":22,"armGroupLabels":34,"otherNames":29},"Observation",[21],[36],{"name":37,"affiliation":38,"role":39},"Peirong Ding, M.D.","Sun Yat-Sen University Cancer Center","PRINCIPAL_INVESTIGATOR",[41],{"name":42,"role":43,"phone":44,"phoneExt":29,"email":45},"Binyi Xiao, M.D","CONTACT","+86-15800004780","xiaoby@sysucc.org.cn",[47],{"facility":48,"status":49,"city":50,"state":51,"zip":52,"country":53,"countryCode":54,"cosmosGeoPoint":55,"geoPoint":60,"contacts":61},"Sun Yat-sen University Cancer Center","RECRUITING","Guangzhou","Guangdong","510060","China","CN",{"type":56,"coordinates":57},"Point",[58,59],113.25,23.11667,{"lat":59,"lon":58},[62],{"name":63,"role":43,"phone":64,"phoneExt":29,"email":45},"Binyi Xiao, M.D.","+86-1580004780",{"type":39,"investigatorFullName":66,"investigatorTitle":67,"investigatorAffiliation":5,"oldNameTitle":29,"oldOrganization":29},"Pei-Rong Ding","Director of the Department of Colorectal Surgery","100652612","research-on-colorectal-cancer-recurrence-monitoring-and-individualized-treatment-based-on-mrd-100652612",false,"NCT07775950","Research on Colorectal Cancer Recurrence Monitoring and Individualized Treatment Based on MRD","Inclusion Criteria:\n\n1. Voluntary participation in the study and provision of written informed consent.\n2. Age ≥18 years at the time of signing informed consent.\n3. Histologically confirmed colorectal adenocarcinoma with mismatch repair deficiency (dMMR) or microsatellite instability-high (MSI-H) status.\n4. Clinically confirmed stage IV disease.\n5. No prior immunotherapy for the current colorectal cancer.\n6. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.\n7. Availability of adequate pretreatment tumor tissue and peripheral blood samples for whole-exome sequencing (WES) and personalized circulating tumor DNA (ctDNA)\u002FMRD analysis.\n8. Life expectancy \\>12 months.\n9. Willing and able to comply with the study procedures and scheduled follow-up.\n\nExclusion Criteria:\n\n1. Presence of another malignancy.\n2. Prior immunotherapy for the current stage IV colorectal cancer.\n3. Organ transplantation within 3 months before enrollment.\n4. History of blood transfusion within 3 months before enrollment.\n5. Active, known, or suspected autoimmune disease, or evidence of active or chronic infection with hepatitis B virus, hepatitis C virus, or human immunodeficiency virus (HIV).\n6. Pregnancy or breastfeeding.\n7. Presence of a serious concurrent disease that, in the investigator's judgment, may substantially affect life expectancy or study participation.\n8. Failure to provide written informed consent.\n9. Any other condition that, in the investigator's judgment, makes the participant unsuitable for enrollment.",true,"ALL","18 Years",{"count":78,"type":79},100,"ESTIMATED","INTERVENTIONAL",[82],"NA","This study aims to evaluate whether plasma molecular residual disease (MRD), assessed using circulating tumor DNA (ctDNA), can help optimize the duration of immunotherapy in patients with metastatic microsatellite instability-high (MSI-H) or mismatch repair-deficient (dMMR) colorectal cancer.\n\nPatients with MSI-H\u002FdMMR metastatic colorectal cancer can achieve durable responses to immune checkpoint inhibitors, but the optimal duration of treatment remains uncertain. Prolonged immunotherapy may increase treatment burden and the risk of immune-related adverse events. ctDNA-based MRD testing may provide a sensitive method for detecting residual tumor burden and identifying patients who may be able to safely stop treatment.\n\nIn this study, patients receiving immunotherapy will undergo serial plasma MRD testing. After completing 1 year of immunotherapy, patients with two consecutive negative MRD results will be randomly assigned to either continue immunotherapy or stop treatment and enter observation. Patients will then be followed every 3 months for 2 years with MRD testing and routine clinical assessments, including imaging and laboratory examinations.\n\nThe study will compare clinical outcomes between the two groups and evaluate whether serial plasma MRD monitoring can support a more individualized approach to the duration of immunotherapy in MSI-H\u002FdMMR metastatic colorectal cancer.",[85,86],"Colorectal Cancer (MSI-H)","Molecular Residual Disease","2026-08-16",{"date":89,"type":90},"2026-08-20","ACTUAL",{"date":92,"type":90},"2026-06-23",{"date":94,"type":79},"2034-12-30",{"name":5,"class":6},1]