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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: |
ChiCTR2600121839 |
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最近更新日期: Date of Last Refreshed on: |
2026-04-03 16:53:50 |
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注册时间: Date of Registration: |
2026-04-03 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: |
一项免疫检查点抑制剂治疗肿瘤患者所致心肌炎的前瞻性、多中心临床研究 |
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Public title: |
A prospective, multicenter clinical study on myocarditis induced by immune checkpoint inhibitor therapy in tumor patients |
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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: |
一项免疫检查点抑制剂治疗肿瘤患者所致心肌炎的前瞻性、多中心临床研究 |
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Scientific title: |
A prospective, multicenter clinical study on myocarditis induced by immune checkpoint inhibitor therapy in tumor patients |
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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: |
禇晓源 |
研究负责人: |
禇晓源,王峰 |
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Applicant: |
Xiaoyuan Chu |
Study leader: |
Xiaoyuan Chu,Feng Wang |
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申请注册联系人电话: Applicant telephone: |
+86 137 7064 8777 |
研究负责人电话:
Study leader's |
+86 137 7064 8777 |
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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: |
chuxiaoyuan00@gmail.com |
研究负责人电子邮件: Study leader's E-mail: |
chuxiaoyuan00@gmail.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: |
江苏省南京中山东路305号 |
研究负责人通讯地址: |
江苏省南京中山东路305号 |
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Applicant address: |
No. 305 Zhongshan East Road, Nanjing, Jiangsu Province |
Study leader's address: |
No. 305 Zhongshan East Road, Nanjing, Jiangsu 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: |
中国人民解放军东部战区总医院 |
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Applicant's institution: |
Eastern Theater General Hospital of the Chinese People's Liberation Army |
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研究负责人所在单位: |
中国人民解放军东部战区总医院 |
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Affiliation of the Leader: |
Eastern Theater General Hospital of the Chinese People's Liberation Army |
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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: |
DZQH-KYLLFS-26-01 |
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: |
中国人民解放军东部战区总医院临床研究伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Clinical Research, Eastern Theater General Hospital of the Chinese People's Liberation Army |
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伦理委员会批准日期: Date of approved by ethic committee: |
2026-03-21 00:00:00 | ||
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伦理委员会联系人: |
吴琼 |
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Contact Name of the ethic committee: |
Qiong Wu |
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伦理委员会联系地址: |
江苏省南京市玄武区中山东路305号 |
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Contact Address of the ethic committee: |
No. 305, Zhongshan East Road, Xuanwu District, Nanjing City, Jiangsu Province |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 25 8086 3234 |
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: |
中国人民解放军东部战区总医院 |
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Primary sponsor: |
Eastern Theater General Hospital of the Chinese People's Liberation Army |
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研究实施负责(组长)单位地址: |
江苏省南京中山东路305号 |
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Primary sponsor's address: |
No. 305 Zhongshan East Road, Nanjing, Jiangsu 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: |
自筹 |
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Source(s) of funding: |
Self-funded |
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研究疾病: |
实体肿瘤 |
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Target disease: |
Solid tumor |
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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: |
1.明确主动监测策略下中国人群中ICIs相关心肌炎的发生情况、临床治疗现状及临床结局; 2.评估真实世界临床实践中《中国临床肿瘤学会肿瘤心脏病学临床实践指南2025》的依从性及规范化用药实施情况; 3.探索性分析细胞因子、淋巴细胞亚群等生物标志物在ICIs相关心肌炎中的预测及预后评估意义。 |
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Objectives of Study: |
1. Clarify the incidence, current clinical treatment status and clinical outcomes of ICIs-related myocarditis in the Chinese population under the active surveillance strategy; 2. Evaluate the compliance with the *Chinese Society of Clinical Oncology Clinical Practice Guidelines for Cardio-Oncology 2025* and the implementation of standardized medication in real-world clinical practice; 3. Conduct an exploratory analysis of the predictive and prognostic evaluation significance of biomarkers such as cytokines and lymphocyte subsets in ICIs-related myocarditis. |
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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. 经细胞学或组织学病理检查明确诊断为实体肿瘤的患者; 2. 计划接受免疫检查点抑制剂(ICIs)治疗方案至少一个周期(包括单药治疗和联合治疗方案,ICIs主要包括PD-1/PD-L1抑制剂、CTLA-4抑制剂、PD-1+VEGF双特异性抗体、PD-1+CTLA-4双抗(双特异性抗体或组合双抗)等,细胞输注类治疗如DC、CIK及CAR-T除外; 3. 认知功能正常,能够理解并完成研究要求的患者不良反应问卷及相关量表; 4. 自愿签署本知情同意书。 |
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Inclusion criteria |
1. Patients with a confirmed diagnosis of solid tumor via cytological or histological pathological examination; 2. Patients scheduled to receive at least one cycle of immune checkpoint inhibitor (ICIs) therapy (including monotherapy and combination therapy regimens; ICIs mainly include PD-1/PD-L1 inhibitors, CTLA-4 inhibitors, PD-1+VEGF bispecific antibodies, PD-1+CTLA-4 bispecific antibodies (bispecific antibodies or combined dual antibodies), etc., excluding cell infusion therapies such as DC, CIK, and CAR-T); 3. Patients with normal cognitive function who can understand and complete the patient adverse reaction questionnaires and relevant scales required by the study; 4. Patients who have voluntarily signed this informed consent form. |
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排除标准: |
1.严重心血管基础疾病(II级以上的充血性心力衰竭、不稳定型心绞痛、心肌梗死、控制不良的心律失常); 2.曾行左胸或心脏放疗、心脏手术(包括支架、瓣膜等手术); 3.有明显的精神障碍,研究者判断无法完成研究; 4.依从性较差或研究者判断无法完成研究的任何情况。 |
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Exclusion criteria: |
1. Severe cardiovascular underlying diseases (Class II or above congestive heart failure, unstable angina pectoris, myocardial infarction, uncontrolled arrhythmias); 2. Previous radiotherapy to the left chest or heart, or heart surgery (including stent, valve, etc. surgeries); 3. Severe mental disorders, as judged by the researchers, that prevent the participant from completing the study; 4. Poor compliance or the researchers' judgment that the participant is unable to complete the study in any circumstances. |
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研究实施时间: Study execute time: |
从 From 2026-03-27 00:00:00至 To 2027-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-04-03 00:00:00 至 To 2027-10-27 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: |
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 |
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: |
EDC |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
EDC |
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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 |