[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100637461":3},{"organization":4,"armGroups":7,"interventions":22,"overallOfficials":27,"centralContacts":39,"locations":27,"responsibleParty":45,"collaborators":27,"id":48,"slug":49,"hasResults":50,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":27,"eligibilityCriteria":54,"healthyVolunteers":50,"sex":55,"minAge":56,"maxAge":27,"enrollmentInfo":57,"targetDuration":27,"studyType":60,"phases":61,"briefSummary":63,"conditions":64,"keywords":68,"overallStatus":71,"whyStopped":27,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":27},{"fullName":5,"class":6},"Fudan University","OTHER",[8,17],{"label":9,"type":10,"description":11,"interventionNames":12},"SHR-1701 induction Group","EXPERIMENTAL","SHR-1701 combined with platinum-doublet chemotherapy induction therapy followed by concurrent chemoradiotherapy and SHR-1701 consolidation therapy.",[13,14,15,16],"Drug: SHR-1701 combined with platinum-doublet chemotherapy induction therapy","Drug: SHR-1701 consolidation therapy","Drug: Platinum-doublet chemotherapy","Radiation: radiotherapy",{"label":18,"type":19,"description":20,"interventionNames":21},"Control Group","ACTIVE_COMPARATOR","Standard concurrent chemoradiotherapy followed by SHR-1701 consolidation therapy",[14,15,16],[23,28,31,34],{"type":24,"name":25,"description":25,"armGroupLabels":26,"otherNames":27},"DRUG","SHR-1701 combined with platinum-doublet chemotherapy induction therapy",[9],null,{"type":24,"name":29,"description":29,"armGroupLabels":30,"otherNames":27},"SHR-1701 consolidation therapy",[18,9],{"type":24,"name":32,"description":32,"armGroupLabels":33,"otherNames":27},"Platinum-doublet chemotherapy",[18,9],{"type":35,"name":36,"description":37,"armGroupLabels":38,"otherNames":27},"RADIATION","radiotherapy","Thoracic concurrent radiotherapy, total dose 60 Gy ±10%",[18,9],[40],{"name":41,"role":42,"phone":43,"phoneExt":27,"email":44},"Zhengfei Zhu","CONTACT","+8618017312901","fuscczzf@163.com",{"type":46,"investigatorFullName":41,"investigatorTitle":47,"investigatorAffiliation":5,"oldNameTitle":27,"oldOrganization":27},"PRINCIPAL_INVESTIGATOR","Professor","100637461","phase-2-shr-1701-for-induction-and-consolidation-therapy-in-unresectable-stage-iii-non-small-cell-lung-cancer-100637461",false,"NCT07619911","SHR-1701 for Induction and Consolidation Therapy in Unresectable Stage III Non-Small Cell Lung Cancer","SHR-1701 for Induction and Consolidation Therapy in Unresectable Stage III Non-Small Cell Lung Cancer: A Randomized, Phase II Clinical Trial","Inclusion Criteria:\n\n* Age ≥18 years, male or female.\n* Baseline ECOG performance status 0-1.\n* Histologically or cytologically confirmed unresectable stage III NSCLC\n* Life expectancy ≥3 months\n* No prior anti-tumor therapy\n* No known EGFR\u002FALK\u002FROS1 sensitive mutations\n* At least one measurable lesion according to RECIST v1.1\n* Adequate organ function\n* Signed informed consent\n\nExclusion Criteria:\n\n* Mixed small-cell and non-small-cell lung cancer histology\n* Known EGFR\u002FALK\u002FROS1 mutations\n* Prior systemic anti-cancer therapy within 4 weeks\n* Active autoimmune disease requiring systemic treatment\n* Active infection including uncontrolled HBV, HCV or HIV infection\n* Significant cardiovascular disease\n* Uncontrolled hypertension\n* Pregnancy or breastfeeding\n* Participation in another interventional clinical trial","ALL","18 Years",{"count":58,"type":59},84,"ESTIMATED","INTERVENTIONAL",[62],"PHASE2","This randomized phase II exploratory clinical study aims to evaluate the efficacy and safety of SHR-1701 in patients with unresectable stage III non-small cell lung cancer (NSCLC). A total of 84 eligible patients will be randomized 1:1 into an induction immunotherapy group or a consolidation immunotherapy group. Group A will receive SHR-1701 combined with platinum-based chemotherapy as induction therapy followed by concurrent chemoradiotherapy (cCRT) and subsequent SHR-1701 consolidation therapy, while Group B will receive standard cCRT followed by SHR-1701 consolidation therapy. The primary endpoint is progression-free survival (PFS). Secondary endpoints include objective response rate (ORR), disease control rate (DCR), overall survival (OS), and safety outcomes.",[65,66,67],"NSCLC Stage III","SHR-1701","Chemoradiotherapy",[69,66,70],"NSCLC","chemoradiotherapy","NOT_YET_RECRUITING","2026-05-27",{"date":74,"type":75},"2026-06-02","ACTUAL",{"date":77,"type":59},"2026-07",{"date":79,"type":59},"2030-12",{"name":5,"class":6}]