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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: |
ChiCTR2500102649 |
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最近更新日期: Date of Last Refreshed on: |
2025-05-18 16:49:03 |
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注册时间: Date of Registration: |
2025-05-18 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
曲妥珠单抗联合帕妥珠单抗用于HER2阳性乳腺癌新辅助治疗的全国多中心真实世界研究 |
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Public title: |
Trastuzumab combined with Pertuzumab for Neoadjuvant Treatment of HER2-Positive Breast Cancer: A National Multi-Center Real-World Study |
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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: |
曲妥珠单抗联合帕妥珠单抗用于HER2阳性乳腺癌新辅助治疗的全国多中心真实世界研究 |
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Scientific title: |
Trastuzumab combined with Pertuzumab for Neoadjuvant Treatment of HER2-Positive Breast Cancer: A National Multi-Center Real-World Study |
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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: |
齐晓伟 |
研究负责人: |
齐晓伟 |
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Applicant: |
Xiaowei Qi |
Study leader: |
Xiaowei Qi |
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申请注册联系人电话: Applicant telephone: |
+86 135 2754 5423 |
研究负责人电话:
Study leader's |
+86 135 2754 5423 |
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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: |
qxw9908@foxmail.com |
研究负责人电子邮件: Study leader's E-mail: |
qxw9908@foxmail.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: |
重庆市沙坪坝区高滩岩正街29号 |
研究负责人通讯地址: |
重庆市沙坪坝区高滩岩正街29号 |
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Applicant address: |
29 Gaotanyan Main street, Shapingba District, Chongqing |
Study leader's address: |
29 Gaotanyan Main street, Shapingba District, Chongqing |
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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: |
重庆市沙坪坝区高滩岩正街29号 |
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Applicant's institution: |
29 Gaotanyan Main street, Shapingba District, Chongqing |
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研究负责人所在单位: |
重庆市沙坪坝区高滩岩正街29号 |
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Affiliation of the Leader: |
29 Gaotanyan Main street, Shapingba District, Chongqing |
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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: |
(B)KY2022170 |
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: |
中国人民解放军陆军军医大学第一附属医院伦理委员会 |
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Name of the ethic committee: |
The First Affiliated Hospital of the Army Medical University, Ethics Committee. |
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伦理委员会批准日期: Date of approved by ethic committee: |
2022-08-31 00:00:00 | ||
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伦理委员会联系人: |
毛青 |
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Contact Name of the ethic committee: |
Qing Mao |
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伦理委员会联系地址: |
重庆市沙坪坝区高滩岩正街29号 |
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Contact Address of the ethic committee: |
29 Gaotanyan Main Street, Shapingba District, Chongqing |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 23 6875 4035 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
陆军军医大学第一附属医院 |
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Primary sponsor: |
The First Affiliated Hospital of Army Medical University |
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研究实施负责(组长)单位地址: |
重庆市沙坪坝区高滩岩正街29号 |
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Primary sponsor's address: |
29 Gaotanyan Main Street, Shapingba District, Chongqing |
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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: |
自筹 |
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Source(s) of funding: |
Self-funded |
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研究疾病: |
HER2阳性乳腺癌 |
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Target disease: |
HER2 positive 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: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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研究设计: |
连续入组 |
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Study design: |
Sequential |
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研究目的: |
评价在中国临床实践中曲妥珠单抗联合帕妥珠单抗及化疗新辅助治疗HER2阳性早期乳腺癌的疗效和安全性。 |
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Objectives of Study: |
Evaluate the efficacy and safety of trastuzumab combined with pertuzumab and chemotherapy as neoadjuvant therapy for HER2-positive early-stage breast cancer in clinical practice in China. |
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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.病理确诊为HER2阳性早期乳腺癌患者; 2.接受HP联合化疗新辅助治疗; 3.2019年 1月~ 2021年12月间于入选中心接受HP联合化疗新辅助治疗; 4.至少有两份完整住院病历的患者; 5.病历有完整的手术和新辅助化疗数据的患者; 6.完整的随访数据。 |
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Inclusion criteria |
1. Pathological diagnosis of HER2 positive early breast cancer patients; 2. Accept HP combined with chemotherapy as neoadjuvant therapy; Received HP combined with chemotherapy neoadjuvant therapy at the selected center between January 2019 and December 2021; 4. Patients with at least two complete hospitalization medical records; 5. Patients with complete surgical and neoadjuvant chemotherapy data in their medical records; 6. Complete follow-up data. |
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排除标准: |
1.合并其他原发恶性肿瘤患者; 2.新辅助治疗期间联用其他治疗手段,如TKI、放疗、免疫治疗等。 |
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Exclusion criteria: |
1. Merge patients with other primary malignant tumors; 2.During the period of neoadjuvant therapy, other treatment methods such as TKI, radiotherapy, immunotherapy, etc. are used in combination. |
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研究实施时间: Study execute time: |
从 From 2022-06-01 00:00:00至 To 2023-06-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2022-08-31 00:00:00 至 To 2022-12-31 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: |
结束 /Completed |
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: |
公开/Public |
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盲法: |
无 |
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Blinding: |
None |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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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): |
研究结束后,通过ResMan(www.medresman.org.cn)方式共享 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
After the end of the study, it was shared by ResMan (www.medresman.org.cn). |
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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: |
病理记录表 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |