[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100539651":3},{"organization":4,"armGroups":7,"interventions":22,"overallOfficials":42,"centralContacts":48,"locations":54,"responsibleParty":82,"collaborators":28,"id":84,"slug":85,"hasResults":86,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":90,"eligibilityCriteria":91,"healthyVolunteers":86,"sex":92,"minAge":93,"maxAge":94,"enrollmentInfo":95,"targetDuration":28,"studyType":98,"phases":99,"briefSummary":101,"conditions":102,"keywords":28,"overallStatus":57,"whyStopped":28,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":108,"completionDateStruct":110,"leadSponsor":112,"locationsCount":113},{"fullName":5,"class":6},"RenJi Hospital","OTHER",[8,17],{"label":9,"type":10,"description":11,"interventionNames":12},"Experimental group","EXPERIMENTAL","The experimental group start with 6 cycles of induction chemohormonal therapy followed with cytoreductive prostatectomy and postoperative adjuvant radiotherapy if needed. All patients continued maintenance therapy.",[13,14,15,16],"Drug: Systemic Chemohormonal Therapy","Drug: Systemic Hormonal Therapy","Procedure: Cytoreductive Prostatectomy","Procedure: Postoperative Adjuvant Radiotherapy",{"label":18,"type":19,"description":20,"interventionNames":21},"Control group","ACTIVE_COMPARATOR","The control group start with 6 cycles of chemohormonal therapy followed by continued maintenance therapy.",[13,14],[23,29,33,38],{"type":24,"name":25,"description":26,"armGroupLabels":27,"otherNames":28},"DRUG","Systemic Chemohormonal Therapy","Under continuous ADT, docetaxel 75mg\u002Fm\\^2 body surface area every 21 days, oral dexamethasone 7.5mg pretreatment 12h, 3h, 1h before each infusion of docetaxel, and a total of 10mg of prednisolone per day when needed according to the decision of the researcher (in the case of grade 3 and above neutropenia or peripheral edema); oral darolutamide 600mg twice per day, 21 days for one cycle, six cycles in total.",[18,9],null,{"type":24,"name":30,"description":31,"armGroupLabels":32,"otherNames":28},"Systemic Hormonal Therapy","Under continuous ADT, oral darolutamide 600mg twice per day",[18,9],{"type":34,"name":35,"description":36,"armGroupLabels":37,"otherNames":28},"PROCEDURE","Cytoreductive Prostatectomy","Cytoreductive prostatectomy was performed after six cycles of neoadjuvant systemic chemohormonal therapy.",[9],{"type":34,"name":39,"description":40,"armGroupLabels":41,"otherNames":28},"Postoperative Adjuvant Radiotherapy","Postoperative adjuvant radiotherapy of prostate bed is performed, if margin positive, with conventional segmentation and the dose of 64-72Gy.",[9],[43,46],{"name":44,"affiliation":5,"role":45},"Yinjie Zhu, Dr.","PRINCIPAL_INVESTIGATOR",{"name":47,"affiliation":5,"role":45},"Liang Dong, Dr.",[49],{"name":50,"role":51,"phone":52,"phoneExt":28,"email":53},"Liang Dong","CONTACT","+86-13601613536","drdongliang@126.com",[55],{"facility":56,"status":57,"city":58,"state":59,"zip":60,"country":61,"countryCode":62,"cosmosGeoPoint":63,"geoPoint":68,"contacts":69},"Renji Hospital, Shanghai Jiao Tong University School of Medicine","RECRUITING","Shanghai","Shanghai Municipality","200127","China","CN",{"type":64,"coordinates":65},"Point",[66,67],121.45806,31.22222,{"lat":67,"lon":66},[70,71,72,73,76,78,80],{"name":47,"role":51,"phone":52,"phoneExt":28,"email":53},{"name":44,"role":45,"phone":28,"phoneExt":28,"email":28},{"name":47,"role":45,"phone":28,"phoneExt":28,"email":28},{"name":74,"role":75,"phone":28,"phoneExt":28,"email":28},"Ruohua Chen, Dr.","SUB_INVESTIGATOR",{"name":77,"role":75,"phone":28,"phoneExt":28,"email":28},"Xinxing Du, Dr.",{"name":79,"role":75,"phone":28,"phoneExt":28,"email":28},"Yanhao Dong, Dr.",{"name":81,"role":75,"phone":28,"phoneExt":28,"email":28},"Hanjing Zhu",{"type":45,"investigatorFullName":50,"investigatorTitle":83,"investigatorAffiliation":5,"oldNameTitle":28,"oldOrganization":28},"Associate Research Fellow","100539651","cytoreductive-prostatectomy-for-poly-metastatic-hormone-sensitive-prostate-cancer-100539651",false,"NCT06306612","CytoREductive prostAtectomy for Poly-metastatic Hormone sensiTIVE Prostate Cancer","Systemic Therapy Combined With Cytoreductive Prostatectomy for the Treatment of de Novo Poly-metastatic Hormone Sensitive Prostate Cancer: A Prospective, Open-label Randomized Controlled Trial","CREATIVE","Inclusion Criteria:\n\n1. Fully understand the purpose of this trial and sign a written informed consent;\n2. Men aged 18-85 years;\n3. have histologically or cytologically confirmed adenocarcinoma of the prostate;\n4. Have multiple metastatic disease, defined as follows: according to RECIST v1.1, metastatic disease was defined as metastatic foci detected on bone scans or measurable lymph nodes or soft tissue or visceral lesions above the aortic bifurcation. Lymph nodes were defined as measurable if their short-axis diameter was ≥15 mm; soft tissue\u002Fvisceral lesions were defined as measurable if their long-axis diameter was ≥10 mm. and total number of metastatic lesions ≥ 5. Patients with only regional lymph node metastases (N1, below the aortic bifurcation) were not eligible for the study.\n5. At the investigator's discretion, patients must meet the indications for ADT and docetaxel;\n6. Patients have not received any prior local or systemic therapy for prostate cancer primary or metastasis.\n7. Eastern Cooperative Oncology Group (ECOG) score of 0-1;\n8. Blood count at screening: hemoglobin ≥ 9.0 g\u002FdL, absolute neutrophil count ≥ 1.5 x 10\\^9\u002FL, and platelet count ≥ 100 x 10\\^9\u002FL (patient has not received any colony-stimulating factor within 4 weeks or a transfusion or blood product within 7 days prior to blood collection)\n9. Serum alanine aminotransferase and\u002For aspartate aminotransferase ≤ 1.5 x Upper limit of normal (ULN), total bilirubin ≤ ULN, creatinine ≤ 2.0 x ULN.\n\nExclusion Criteria:\n\n1. Prior therapy: ADT, second-generation androgen receptor inhibitors, CYP17 enzyme inhibitors, any chemotherapy or immunotherapy for prostate cancer, radiotherapy (external radiation radiotherapy, brachytherapy, or radiopharmaceuticals);\n2. Known hypersensitivity to any of the investigational drugs, or excipients in the preparations;\n3. Contraindication to CT\u002FMRI examination;\n4. Any of the following conditions within 6 months prior to randomization: stroke, myocardial infarction, severe or unstable angina, coronary or peripheral artery bypass grafting, or congestive heart failure (New York Heart Association cardiac function class III or IV);\n5. uncontrolled hypertension as evidenced by a resting systolic blood pressure ≥ 160 mm Hg or diastolic blood pressure ≥ 100 mm Hg after treatment\n6. History of prior malignancy, except basal cell or cutaneous squamous cell carcinoma in complete remission;\n7. History of gastrointestinal disorders or surgery expected to significantly interfere with the absorption of study drug(s);\n8. Active acute and chronic viral hepatitis, known HIV infection;\n9. Prior (28 days prior to initiation of study drug or 5 half-lives of investigational therapy from a prior study, whichever is longer) or concurrent participation in another clinical study of study drug;\n10. Any other serious or unstable medical condition or condition that may interfere with their participation in the study or the evaluation of study results or may jeopardize the safety of the trial and other conditions;\n11. Inability to swallow oral medications;\n12. A close interest in the research center.","MALE","18 Years","85 Years",{"count":96,"type":97},192,"ESTIMATED","INTERVENTIONAL",[100],"NA","The goal of this clinical trial is to compare systemic therapy combined with cytoreductive prostatectomy with standard of care (SOC) in de novo poly-metastatic hormone sensitive prostate cancer (de novo pmHSPC). The main questions it aims to answer are:\n\n1. To explore the clinical benefit and safety of systemic therapy combined with cytoreductive prostatectomy for patients with de novo pmHSPC.\n2. To explore the characteristics of the subgroup of patients who could benefit more from the above treatment.\n3. To explore the relationship between stage efficacy and clinical prognosis.\n4. To explore the correlation between molecular imaging such as PSMA-PET\u002FCT and its changes with treatment efficacy.\n\nParticipants will undergo systemic therapy combined with cytoreductive prostatectomy.\n\nResearchers will compare systemic therapy combined with cytoreductive prostatectomy with SOC to see the pros and cons of the two strategies.",[103],"Prostate Cancer","2026-08-08",{"date":106,"type":107},"2026-08-11","ACTUAL",{"date":109,"type":107},"2024-03-21",{"date":111,"type":97},"2028-12-31",{"name":5,"class":6},1]