[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100595566":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":26,"locations":32,"responsibleParty":46,"collaborators":20,"id":48,"slug":20,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":20,"eligibilityCriteria":52,"healthyVolunteers":49,"sex":53,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":20,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":20,"overallStatus":65,"whyStopped":20,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":75},{"fullName":5,"class":6},"Anhui Provincial Hospital","OTHER_GOV",[8],{"label":9,"type":10,"description":9,"interventionNames":11},"Pronton radiotherapy with chemoimmunotherapy","EXPERIMENTAL",[12,13],"Radiation: Proton radiotherapy","Drug: Immune Checkpoint Inhibitors",[15,21],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"RADIATION","Proton radiotherapy","Patients enrolled would receive proton radiotherapy with chemoimmunotherapy.",[9],null,{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":20},"DRUG","Immune Checkpoint Inhibitors","Patients enrolled would receive proton radiotherapy and chemoimmunotherapy",[9],[27],{"name":28,"role":29,"phone":30,"phoneExt":20,"email":31},"Dong Qian, M.D. & Ph.D.","CONTACT","+8618202269589","qiandong@ustc.edu.cn",[33],{"facility":5,"status":20,"city":34,"state":35,"zip":20,"country":36,"countryCode":37,"cosmosGeoPoint":38,"geoPoint":43,"contacts":44},"Hefei","Anhui","China","CN",{"type":39,"coordinates":40},"Point",[41,42],117.28083,31.86389,{"lat":42,"lon":41},[45],{"name":28,"role":29,"phone":30,"phoneExt":20,"email":31},{"type":47,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR","100595566",false,"NCT07034118","Definitive Proton Radiotherapy Combined With Chemotherapy and Immunotherapy for Locally Advanced Esophageal Squamous Cell Carcinoma: A Phase I Clinical Study","Inclusion Criteria:\n\nAge 18-75 years ECOG performance status 0-1 Histologically confirmed esophageal squamous cell carcinoma (ESCC) Stage II-IVA disease (AJCC 8th edition), confirmed via contrast-enhanced CT of the neck, chest, and abdomen, or PET-CT Unresectable by surgical evaluation or patient refusal of surgery No prior oncologic treatment Life expectancy \\>6 months Radiotherapy plan meets physical dose constraints Signed informed consent by patient or legal representative\n\nExclusion Criteria:\n\nAge \\\u003C18 or \\>75 years ECOG \\>1 or inability to tolerate treatment Histology other than squamous cell carcinoma Stage I or IVB disease High risk of hemorrhage or fistula, as assessed by imaging and radiation oncologists Previously treated patients Life expectancy \\\u003C6 months Contraindications to chemotherapy or immunotherapy Radiotherapy plan fails to meet dose constraints Lack of signed informed consent","ALL","18 Years","75 Years",{"count":57,"type":58},23,"ESTIMATED","INTERVENTIONAL",[61],"PHASE1","The standard treatment for locally advanced esophageal squamous cell carcinoma (ESCC) is definitive concurrent chemoradiotherapy (CCRT). However, conventional photon-based radiotherapy is associated with excessive radiation exposure to normal tissues and a high incidence of treatment-related toxicities. Proton radiotherapy, one of the major advances in radiation oncology in recent years, offers the dosimetric advantage of reduced radiation to surrounding normal tissues, thereby decreasing the rate of adverse events. Two recent clinical studies have suggested that, compared with conventional photon radiotherapy, proton radiotherapy can significantly reduce the incidence of treatment-related toxicities and potentially improve patient survival outcomes.\n\nImmune checkpoint inhibitors (ICIs) have been widely used in both locally advanced and advanced esophageal cancer and have demonstrated promising clinical efficacy. Preliminary results from several ongoing phase III clinical trials indicate that combining ICIs with concurrent chemoradiotherapy is both safe and effective. Moreover, proton radiotherapy, by minimizing the low-dose radiation exposure to circulating peripheral lymphocytes, may better preserve systemic immune function. Therefore, compared to photon therapy, proton radiotherapy may theoretically enhance the synergistic effect when combined with ICIs, offering a potential survival benefit.\n\nBased on this rationale, we propose a phase I clinical trial to investigate the safety and preliminary efficacy of definitive proton chemoradiotherapy combined with immune checkpoint inhibition in patients with locally advanced esophageal squamous cell carcinoma.",[64],"Esophageal Carcinoma","NOT_YET_RECRUITING","2025-06-15",{"date":68,"type":69},"2025-06-24","ACTUAL",{"date":71,"type":58},"2025-08-01",{"date":73,"type":58},"2028-08-31",{"name":5,"class":6},1]