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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2600118253 |
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最近更新日期: Date of Last Refreshed on: |
2026-02-03 17:10:56 |
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注册时间: Date of Registration: |
2026-02-03 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
一项评价ADT+多西他赛+达罗它胺三联治疗方案治疗转移性前列腺癌的真实世界回顾性研究(YHCG-006) |
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Public title: |
A real-world retrospective study evaluating the ADT combined with docetaxel and darolutamide triple therapy regimen for metastatic prostate cancer(YHCG-006) |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
一项评价ADT+多西他赛+达罗它胺三联治疗方案治疗转移性前列腺癌的真实世界回顾性研究(YHCG-006) |
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Scientific title: |
A real-world retrospective study evaluating the ADT combined with docetaxel and darolutamide triple therapy regimen for metastatic prostate cancer(YHCG-006) |
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研究课题代号(代码): Study subject ID: |
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在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
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申请注册联系人: |
马琪 |
研究负责人: |
马琪 |
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Applicant: |
Qi Ma |
Study leader: |
Qi Ma |
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申请注册联系人电话: Applicant telephone: |
+86 574 8708 9078 |
研究负责人电话:
Study leader's |
+86 574 8708 9078 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
fyymaqi@nbu.edu.cn |
研究负责人电子邮件: Study leader's E-mail: |
45112409@qq.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
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申请注册联系人通讯地址: |
浙江省宁波市海曙区柳汀街59号 |
研究负责人通讯地址: |
浙江省宁波市海曙区柳汀街59号 |
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Applicant address: |
No. 59, Liuting Street, Haishu District, Ningbo City, Zhejiang Province |
Study leader's address: |
No. 59, Liuting Street, Haishu District, Ningbo City, Zhejiang Province |
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申请注册联系人邮政编码: Applicant postcode: |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
宁波大学附属第一医院 |
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Applicant's institution: |
The First Affiliated Hospital of Ningbo University |
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研究负责人所在单位: |
宁波大学附属第一医院 |
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Affiliation of the Leader: |
The First Affiliated Hospital of Ningbo University |
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是否获伦理委员会批准: |
是 |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
宁波大学附属第一医院伦审2025研第141A号 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
宁波大学附属第一医院医学伦理委员会 |
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Name of the ethic committee: |
First Affiliated Hospital of Ningbo University Clinical Trial Ethics Committee for Drugs and Medical Devices |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-06-05 00:00:00 | ||
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伦理委员会联系人: |
陈少莹 |
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Contact Name of the ethic committee: |
Chen Shaoying |
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伦理委员会联系地址: |
浙江省宁波市海曙区柳汀街59号 |
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Contact Address of the ethic committee: |
No. 59, Liuting Street, Haishu District, Ningbo City, Zhejiang Province |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 574 87085233 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
sychenjy@163.com |
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研究实施负责(组长)单位: |
宁波大学附属第一医院 |
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Primary sponsor: |
The First Affiliated Hospital of Ningbo University |
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研究实施负责(组长)单位地址: |
浙江省宁波市海曙区柳汀街59号 |
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Primary sponsor's address: |
No. 59, Liuting Street, Haishu District, Ningbo City, Zhejiang Province |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
吴阶平医学基金会 |
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Source(s) of funding: |
Wu Jieping Foundation |
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研究疾病: |
经病理确诊为前列腺腺癌 |
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Target disease: |
prostate cancer |
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研究疾病代码: |
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Target disease code: |
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研究类型: |
观察性研究 |
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Study type: |
Observational study |
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研究所处阶段: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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研究设计: |
队列研究 |
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Study design: |
Cohort study |
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研究目的: |
主要目的: 评价三联疗法(ADT+多西他赛+达罗他胺)治疗转移性前列腺癌(mPC)的有效性 次要目的: 评价三联疗法(ADT+多西他赛+达罗他胺)治疗转移性前列腺癌(mPC)的安全性和耐受性 |
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Objectives of Study: |
Main purpose: To evaluate the efficacy of the triple therapy (ADT + docetaxel + darolutamide) in the treatment of metastatic prostate cancer (mPC) Secondary objective: To evaluate the safety and tolerability of the triple therapy (ADT + docetaxel + darolutamide) in the treatment of metastatic prostate cancer (mPC). |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
1.18岁以上的男性; 2.经病理确诊为前列腺腺癌,经骨扫描、MRI、CT或PET证明有远处转移; 3.雄激素剥夺治疗在达罗他胺治疗前或同时治疗; 4.在达罗他胺治疗期间至少接受1次多西他赛治疗; 5.作为真实世界研究,允许受试者接受手术放疗等局部治疗。 |
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Inclusion criteria |
1. Male, > 18 years; 2. Pathologically confirmed prostate adenocarcinoma, with distant metastases proven by bone scan, MRI, CT, or PET. 3. Androgen deprivation therapy before or during darolutamide treatment; 4. Received at least one dose of docetaxel during darolutamide treatment; 5. As a real-world study, it allows subjects to receive local treatments such as surgery and radiotherapy. |
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排除标准: |
1.前列腺穿刺病理学结果显示存在神经内分泌性前列腺癌,包括小细胞癌; 2.回顾性分析时存在过多临床资料及随访数据不完善者; 3.在诊断为mPC 时患有并发癌症的患者或在诊断为mPC后 6 个月 内接受过针对其他癌症的任何抗癌疗法治疗的患者,非转移性非黑色素瘤皮肤癌或原位或良性肿瘤除外。 |
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Exclusion criteria: |
1. Neuroendocrine prostate cancer or small cell prostate cancer; 2. Lack of enough clinical data or lost of follow up; 3. Patients with concurrent cancers at the time of diagnosis of mPC or who have received any anti-cancer therapy for other cancers within 6 months after diagnosis of mPC, except for non-metastatic non-melanoma skin cancer or in situ or benign tumors. |
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研究实施时间: Study execute time: |
从 From 2026-01-01 00:00:00至 To 2026-06-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-03-01 00:00:00 至 To 2026-04-30 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
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性别: |
男性 |
Gender: |
Male |
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随机方法(请说明由何人用什么方法产生随机序列): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
不公开/Private |
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盲法: |
无 |
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Blinding: |
None |
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是否共享原始数据: IPD sharing |
是Yes |
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共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
共享,向主要研究者索取 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Ask for principle investigator |
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数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
病例报告表 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |