[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100569985":3},{"organization":4,"armGroups":7,"interventions":24,"overallOfficials":30,"centralContacts":39,"locations":45,"responsibleParty":61,"collaborators":30,"id":65,"slug":66,"hasResults":67,"nctId":68,"briefTitle":69,"officialTitle":70,"acronym":30,"eligibilityCriteria":71,"healthyVolunteers":67,"sex":72,"minAge":73,"maxAge":74,"enrollmentInfo":75,"targetDuration":30,"studyType":78,"phases":79,"briefSummary":81,"conditions":82,"keywords":84,"overallStatus":48,"whyStopped":30,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":96},{"fullName":5,"class":6},"Ruijin Hospital","OTHER",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Cluster1 DEL：CR-CHOP+PD1 inhibitor","EXPERIMENTAL","Participants who met the inclusion\u002Fexclusion criteria signed informed consent and received 1 course of CR-CHOP, followed by stratification of the remaining 5 cycles based on genetic subtypes. C1 plus PD1 inhibitor.",[13],"Drug: CR-CHOP+PD1 inhibitor",{"label":15,"type":10,"description":16,"interventionNames":17},"Cluster 2 and 3 DEL：CR-CHOP plus Orelabrutinib","Participants who met the inclusion\u002Fexclusion criteria signed informed consent and received 1 course of CR-CHOP, followed by stratification of the remaining 5 cycles based on genetic subtypes. C2 and C3 were treated with Orelabrutinib.",[18],"Drug: CR-CHOP + Orelabrutinib",{"label":20,"type":10,"description":21,"interventionNames":22},"Tp53 mut DEL：CR-CHOP plus Decitabine","Participants who met the inclusion\u002Fexclusion criteria signed informed consent and received 1 course of CR-CHOP, followed by stratification of the remaining 5 cycles based on genetic subtypes.TP53mut plus decitabine.",[23],"Drug: CR-CHOP + decitabine",[25,31,35],{"type":26,"name":27,"description":28,"armGroupLabels":29,"otherNames":30},"DRUG","CR-CHOP+PD1 inhibitor","Rituximab 375 mg\u002Fm2 D1； Cyclophosphamide 750mg\u002Fm2 D2； Doxorubicin 50mg\u002Fm2 D2； Vincristine 1.4 mg\u002Fm2 D2； Prednisone 60 mg\u002Fm2 D2-6； Chidamide 20mg\u002Fd D1,4,8,11； PD1 200mg D1",[9],null,{"type":26,"name":32,"description":33,"armGroupLabels":34,"otherNames":30},"CR-CHOP + Orelabrutinib","Rituximab 375 mg\u002Fm2 D1； Cyclophosphamide 750mg\u002Fm2 D2； Doxorubicin 50mg\u002Fm2 D2； Vincristine 1.4 mg\u002Fm2 D2； Prednisone 60 mg\u002Fm2 D2-6； Chidamide 20mg\u002Fd D1,4,8,11； Orelabrutinib 150mg\u002Fqd D1-21",[15],{"type":26,"name":36,"description":37,"armGroupLabels":38,"otherNames":30},"CR-CHOP + decitabine","Rituximab 375 mg\u002Fm2 D1； Cyclophosphamide 750mg\u002Fm2 D2； Doxorubicin 50mg\u002Fm2 D2； Vincristine 1.4 mg\u002Fm2 D2； Prednisone 60 mg\u002Fm2 D2-6； Chidamide 20mg\u002Fd D1,4,8,11； Decitabine 10mg\u002Fm2 D-5 - -1",[20],[40],{"name":41,"role":42,"phone":43,"phoneExt":30,"email":44},"Li Wang","CONTACT","18917762217","dr_wangli@126.com",[46],{"facility":47,"status":48,"city":49,"state":50,"zip":30,"country":51,"countryCode":52,"cosmosGeoPoint":53,"geoPoint":58,"contacts":59},"No. 197 Ruijin 2nd Road, Huangpu District, Shanghai","RECRUITING","Shanghai","Shanghai Municipality","China","CN",{"type":54,"coordinates":55},"Point",[56,57],121.45806,31.22222,{"lat":57,"lon":56},[60],{"name":41,"role":42,"phone":43,"phoneExt":30,"email":44},{"type":62,"investigatorFullName":63,"investigatorTitle":64,"investigatorAffiliation":5,"oldNameTitle":30,"oldOrganization":30},"PRINCIPAL_INVESTIGATOR","Zhao Weili","Principal Investigator","100569985","phase-2-cr-chopx-in-previously-untreated-del-100569985",false,"NCT06701357","CR-CHOP+X in Previously Untreated DEL","A Prospective, Open-label Phase II Study of Chidamide Plus R-CHOP + X in Previously Untreated Diffuse Large B-cell Lymphoma with Double Expression of MYC and BCL2.","Inclusion Criteria:\n\n* 1\\. Histologically confirmed diffuse large B-cell lymphoma with CD20 positive;\n* 2\\. MYC and BCL2 are expressed simultaneously, WHO immunohistochemical standards: MYC≥40%, BCL2 ≥50%;\n* 3\\. Age ≥ 18 years old, ≦75 years old;\n* 4\\. ECOG physical status score of 0, 1 or 2;\n* 5\\. No previous history of malignant tumors; No other tumors occurred simultaneously;\n* 6\\. Patients judged by the investigator to have a life expectancy of at least 6 months;\n* 7\\. The patient or his legal representative must provide written informed consent prior to any research special examination or procedure;\n* 8\\. International prognostic Index (IPI) \\>1 score.\n\nExclusion Criteria:\n\n* 1\\. Have previously received systemic or local treatment including chemotherapy;\n* 2\\. Previously received autologous stem cell transplantation;\n* 3\\. Previous history of other malignant tumors, except skin basal cell carcinoma and cervical carcinoma in situ;\n* 4\\. Accompanied by uncontrolled cardiovascular and cerebrovascular diseases, coagulation disorders, connective tissue diseases, serious infectious diseases and other diseases;\n* 5\\. Primary central nervous system lymphoma;\n* 6\\. Left ventricular ejection fraction ≤ 50%;\n* 7\\. Laboratory test values at the time of screening (unless due to lymphoma): A. Neutrophils \\\u003C1.5\\*109\u002FL; B. Platelet \\\u003C75\\*109\u002FL; C. ALT or AST were 2 times higher than the upper limit of normal, AKP and bilirubin were 1.5 times higher than the upper limit of normal; D. Creatinine levels higher than 1.5 times the upper limit of normal;\n* 8\\. Other concurrent and uncontrolled medical conditions that the investigator believes will affect patient participation in the study;\n* 9\\. Patients with mental illness or other patients known or suspected to be unable to fully comply with the study protocol;\n* 10\\. Pregnant or lactating women;\n* 11\\. People living with HIV;\n* 12\\. Patients with positive HbsAg test results need to undergo HBV DNA test, and can be enrolled before turning negative. In addition, if the HBsAg test result is negative, but the HBcAb test is positive (regardless of the HBsAb status), HBV DNA test should also be performed. If the result is positive, the treatment should also be negative before admission.","ALL","18 Years","75 Years",{"count":76,"type":77},49,"ESTIMATED","INTERVENTIONAL",[80],"PHASE2","This is a prospective, single-arm, open-label phase II clinical trial that evaluates the efficacy and safety of CR-CHOP regimen combined with different targeted drugs based on different molecular subtypes in newly diagnosed DEL patients.",[83],"DLBCL",[83,85,86],"double-expression","chidamide","2024-12-26",{"date":89,"type":90},"2024-12-30","ACTUAL",{"date":92,"type":90},"2024-12-10",{"date":94,"type":77},"2028-12-01",{"name":5,"class":6},1]