[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100468881":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":11,"centralContacts":20,"locations":30,"responsibleParty":50,"collaborators":11,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":11,"eligibilityCriteria":60,"healthyVolunteers":56,"sex":61,"minAge":62,"maxAge":11,"enrollmentInfo":63,"targetDuration":11,"studyType":66,"phases":67,"briefSummary":69,"conditions":70,"keywords":11,"overallStatus":33,"whyStopped":11,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":81},{"fullName":5,"class":6},"Asan Medical Center","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"5 years of adjuvant imatinib treatment","EXPERIMENTAL",null,[13],"Drug: Imatinib Mesylate",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":11},"DRUG","Imatinib Mesylate","Imatinib Mesylate, 400 mg once daily, oral. 5 years of adjuvant imatinib treatment (standard treatment 3years + IP treatment : 2yesrs)",[9],[21,26],{"name":22,"role":23,"phone":24,"phoneExt":11,"email":25},"Ryu Min-Hee, MD, PhD","CONTACT","82-2-3010-5936","miniryu@amc.seoul.kr",{"name":27,"role":23,"phone":28,"phoneExt":11,"email":29},"Kang Yoon-Koo, MD, PhD","82-2-3010-3230","ykkang@amc.seoul.kr",[31],{"facility":32,"status":33,"city":34,"state":34,"zip":35,"country":36,"countryCode":11,"cosmosGeoPoint":37,"geoPoint":42,"contacts":43},"Asan Medical Center, University of Ulsan College of Medicine","RECRUITING","Seoul","138-736","South Korea",{"type":38,"coordinates":39},"Point",[40,41],126.9784,37.566,{"lat":41,"lon":40},[44,47],{"name":45,"role":23,"phone":46,"phoneExt":11,"email":29},"Yoon-Koo Kang, MD, PhD","+82-2-3010-3230",{"name":48,"role":23,"phone":49,"phoneExt":11,"email":25},"Min-Hee Ryu, MD, PhD","+82-2-3010-5935",{"type":51,"investigatorFullName":52,"investigatorTitle":53,"investigatorAffiliation":5,"oldNameTitle":11,"oldOrganization":11},"PRINCIPAL_INVESTIGATOR","Min-Hee Ryu","Professor","100468881","phase-2-5-years-of-adjuvant-imatinib-in-patients-with-gastrointestinal-stromal-tumor-with-a-high-risk-100468881",false,"NCT05385549","5 Years of Adjuvant Imatinib in Patients With Gastrointestinal Stromal Tumor With a High Risk","A Phase 2 Study of 5 Years of Adjuvant Imatinib in Patients With Gastrointestinal Stromal Tumor With a High Risk of Recurrence Following Surgical Resection","Inclusion Criteria:\n\n1. Age 20 years or older, at the time of acquisition of informed consent\n2. Histologically confirmed GIST with CD117(+), DOG-1(+), or mutation in KIT or PDGFRα gene\n3. (1) Completely resected localized GIST (R0 resection) within 12 weeks prior to the start of the adjuvant imatinib.\n\n(2) After complete resection(R0 resection), High risk GIST according to Modified NIH criteria and ongoing adjuvant imatinib treatment.\n\n4\\) High risk GIST according to Modified NIH criteria,\n\n1. Tumor rupture according to Nishida classification or\n2. tumor size \\>10cm and mitosis \\>10\u002F50 HPF 5) Eastern Cooperative Oncology Group (ECOG) performance status 0 \\~ 2 6) Adequate bone marrow, hepatic, renal, and other organ functions, before adjuvant imatinib treatment\n\n   * Neutrophil \\>1,500\u002Fmm3\n   * Platelet \\> 100,000\u002Fmm3\n   * Hemoglobin \\>8.0 g\u002FdL\n   * Total bilirubin \\\u003C 1.5 x upper limit of normal (ULN)\n   * AST\u002FALT \\\u003C 2.5 x ULN\n   * Creatinine \\\u003C1.5 x ULN 7) Provision of a signed written informed consent\n\nExclusion Criteria:\n\n1. Women of child-bearing potential who are pregnant or breast feeding\n2. Women or men who are not willing to use effective contraception entering the study period or until at least 3 months after the last study drug administration.\n3. If any of the following applies within ≤ 6 months prior to starting study enrollment : Myocardial Infarction, severe instable angina, coronary\u002Fperipheral bypass, NYHA class III or IV congestive heart failure, stroke or transient ischemic attack, treatment required severe arrhythmia.\n4. Uncontrolled infection\n5. Acute and chronic liver disease and all chronic liver impairment.(But Patients with stable chronic hepatitis B are eligible)\n6. Patients who had reduced the dose of imatinib to less than 300 mg\u002Fday due to toxicity.\n7. Acute, or chronic medical or psychiatric condition or laboratory abnormality such as active uncontrolled infection that difficult to study participation in the judgment of the investigator\n8. Known diagnosis of HIV infection (HIV testing is not mandatory).\n9. History of another primary malignancy that is currently clinically significant or currently requires active intervention.\n10. Alcohol or substance abuse disorder.\n11. The patients with PDGFRα D842V mutation","ALL","20 Years",{"count":64,"type":65},35,"ESTIMATED","INTERVENTIONAL",[68],"PHASE2","In this study, the investigators aim to investigate the efficacy and safety of 5 years of adjuvant imatinib treatment in patients with tumor rupture defined by Nishida classification or those with a tumor size 10cm or larger and a mitotic index of 10\u002F50HPFs or higher.",[71],"Gastrointestinal Stromal Tumors","2025-08-05",{"date":74,"type":75},"2025-08-08","ACTUAL",{"date":77,"type":75},"2022-09-07",{"date":79,"type":65},"2030-04-30",{"name":5,"class":6},1]