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注册号: Registration number: |
ChiCTR2500103653 |
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最近更新日期: Date of Last Refreshed on: |
2025-06-03 14:49:24 |
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注册时间: Date of Registration: |
2025-06-03 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: |
基于真实世界数据的THP与TH+TKI方案治疗HER2阳性晚期乳腺癌的临床综合评价研究 |
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Public title: |
A clinical comprehensive evaluation study of THP and TH+TKI regimens for the treatment of HER2-positive advanced breast cancer based on real-world data |
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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: |
基于真实世界数据的THP与TH+TKI方案治疗HER2阳性晚期乳腺癌的临床综合评价研究 |
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Scientific title: |
A clinical comprehensive evaluation study of THP and TH+TKI regimens for the treatment of HER2-positive advanced breast cancer based on real-world data |
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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: |
郭维 |
研究负责人: |
张玉 |
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Applicant: |
Wei Guo |
Study leader: |
Yu Zhang |
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申请注册联系人电话: Applicant telephone: |
+86 18771128226 |
研究负责人电话:
Study leader's |
+86 27 85726685 |
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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: |
guoweixtao@hust.edu.cn |
研究负责人电子邮件: Study leader's E-mail: |
whxhzy@163.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: |
湖北省武汉市江汉区解放大道1277号 |
研究负责人通讯地址: |
湖北省武汉市江汉区解放大道1277号 |
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Applicant address: |
No.1277 Jiefang Avenue, Jianghan District, Wuhan City, Hubei Province |
Study leader's address: |
No.1277 Jiefang Avenue, Jianghan District, Wuhan City, Hubei 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: |
华中科技大学同济医学院附属协和医院 |
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Applicant's institution: |
Huazhong University of Science and Technology Tongji Medical College Affiliated Union Hospital |
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研究负责人所在单位: |
华中科技大学同济医学院附属协和医院 |
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Affiliation of the Leader: |
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology |
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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: |
[2025]伦审字(0400-01)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: |
华中科技大学同济医学院附属协和医院医学伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Union Hospital of Tongji Medical College Huazhong University of Science and Technology |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-05-28 00:00:00 | ||
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伦理委员会联系人: |
褚圆圆 |
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Contact Name of the ethic committee: |
Chu Yuanyuan |
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伦理委员会联系地址: |
湖北省武汉市江汉区解放大道1277号 |
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Contact Address of the ethic committee: |
No.1277 Jiefang Avenue, Jianghan District, Wuhan City, Hubei Province |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 27 85726375 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
994877373@qq.com |
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研究实施负责(组长)单位: |
华中科技大学同济医学院附属协和医院 |
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Primary sponsor: |
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology |
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研究实施负责(组长)单位地址: |
湖北省武汉市江汉区解放大道1277号 |
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Primary sponsor's address: |
No.1277 Jiefang Avenue, Jianghan District, Wuhan City, Hubei 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: |
科技基础资源调查专项 |
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Source(s) of funding: |
Clinical Comprehensive Evaluation of Hospital Management Institute of National Health Commission |
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研究疾病: |
HER2阳性晚期乳腺癌 |
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Target disease: |
HER2-positive advanced breast 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: |
本研究旨在通过考察帕妥珠单抗在实际临床应用中出现的ADR/AEs,同时比较THP方案和TH+TKI方案用于HER2阳性晚期乳腺癌治疗的疗效,通过成本-效用、成本-效果进行分析判断各治疗方案经济性,通过文献检索分析、调查问卷评价帕妥珠单抗的创新性、适宜性及可及性,补充完善药品上市前安全性和经济学评价的不足,得出客观科学的评价结论,为临床安全合理用药提供参考,提高我国临床药品治疗水平,为药品生产企业优化生产工艺、修改药品说明书提供证据支撑,医药行政管理部门药品遴选淘汰、行政措施、再注册等提供政策依据。 |
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Objectives of Study: |
This study aims to investigate the adverse drug reactions (ADRs) and adverse events (AEs) of pertuzumab in actual clinical application, compare the efficacy of the THP regimen and the TH + TKI regimen in the treatment of HER2-positive advanced breast cancer, analyze and judge the economic efficiency of each treatment plan through cost-utility and cost-effectiveness analysis, evaluate the innovation, suitability and accessibility of pertuzumab through literature retrieval and questionnaire surveys, supplement and improve the deficiencies of pre-market safety and economic evaluation of drugs, draw objective and scientific evaluation conclusions, provide references for safe and rational drug use in clinical practice, improve the clinical drug treatment level in China, and provide evidence support for drug manufacturers to optimize production processes and modify drug instructions, as well as provide policy basis for drug selection and elimination, administrative measures, and re-registration by medical and pharmaceutical administrative departments. |
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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: |
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Inclusion criteria |
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排除标准: |
1.合并其他恶性肿瘤的患者; |
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Exclusion criteria: |
1.Patients combined with other types of malignant tumors; 2.Patients with severe functional impairments of organs such as the heart, liver and kidneys; 3.Patients who are allergic to the studied drug or its components; 4.Patients who are unable to cooperate with follow-up or complete the questionnaire (such as due to language barriers or mental disorders); 5.Other circumstances that the researchers considered unsuitable for inclusion in the study. |
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研究实施时间: Study execute time: |
从 From 2025-05-01 00:00:00至 To 2026-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-06-09 00:00:00 至 To 2026-10-31 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: |
男女均可 |
Gender: |
Both |
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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 |
否No |
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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): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
None |
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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: |
通过电子数据采集系统(Electronic Data Capture,EDC),采用电子病例报告表(Electronic Case Report Form,eCRF)代替纸质病例报告表来对临床试验数据进行收集和管理 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Through the Electronic Data Capture (EDC) system, electronic case report forms (eCRF) are used instead of paper case report forms to collect and manage clinical trial data |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |