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注册号: Registration number: |
ChiCTR2600124408 |
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最近更新日期: Date of Last Refreshed on: |
2026-05-12 09:51:11 |
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注册时间: Date of Registration: |
2026-05-12 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: |
一项真实世界回顾性研究:泽贝妥单抗/利妥昔单抗联合 CHOP(HI-CHOP/R-CHOP)治疗初治弥漫性大B细胞淋巴瘤(DLBCL)的长期随访研究 |
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Public title: |
A Long-term Follow-up Retrospective Study of Zebetuximab/Rituximab Combined with CHOP (HI-CHOP/R-CHOP) in the Treatment of Newly Diagnosed Diffuse Large B-Cell Lymphoma (DLBCL) |
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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: |
一项真实世界回顾性研究:泽贝妥单抗/利妥昔单抗联合 CHOP(HI-CHOP/R-CHOP)治疗初治弥漫性大B细胞淋巴瘤(DLBCL)的长期随访研究 |
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Scientific title: |
A Long-term Follow-up Retrospective Study of Zebetuximab/Rituximab Combined with CHOP (HI-CHOP/R-CHOP) in the Treatment of Newly Diagnosed Diffuse Large B-Cell Lymphoma (DLBCL) |
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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: |
李志铭 |
研究负责人: |
李志铭 |
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Applicant: |
Li Zhiming |
Study leader: |
Li Zhiming |
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申请注册联系人电话: Applicant telephone: |
+86 13719189172 |
研究负责人电话:
Study leader's |
+86 20 87343765 |
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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: |
lizhm@sysucc.org.cn |
研究负责人电子邮件: Study leader's E-mail: |
lizhm@sysucc.org.cn |
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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: |
中国广东省广州市越秀区东风东路651号先烈南路青菜岗21号 |
研究负责人通讯地址: |
中国广东省广州市越秀区东风东路651号先烈南路青菜岗21号 |
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Applicant address: |
No.651 Dongfeng East Road, No.21 Qingcaigang Xianlie South Road, Yuexiu District, Guangzhou, Guangdong, China |
Study leader's address: |
No.651 Dongfeng East Road, No.21 Qingcaigang Xianlie South Road, Yuexiu District, Guangzhou, Guangdong, China |
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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: |
中山大学肿瘤防治中心 |
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Applicant's institution: |
Sun Yat-sen University Cancer Center |
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研究负责人所在单位: |
中山大学肿瘤防治中心 |
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Affiliation of the Leader: |
Sun Yat-sen University Cancer Center |
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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: |
B2026-093-01 |
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: |
中山大学肿瘤防治中心伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Sun Yat-sen University Cancer Center |
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伦理委员会批准日期: Date of approved by ethic committee: |
2026-02-10 00:00:00 | ||
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伦理委员会联系人: |
潘旭芝 |
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Contact Name of the ethic committee: |
Pan Xuzhi |
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伦理委员会联系地址: |
中国广东省广州市越秀区东风东路651号、先烈南路青菜岗21号 |
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Contact Address of the ethic committee: |
No.651 Dongfeng East Road, No.21 Qingcaigang Xianlie South Road, Yuexiu District, Guangzhou, Guangdong, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 20 87343009 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
panxzh@sysucc.org.cn |
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研究实施负责(组长)单位: |
中山大学肿瘤防治中心 |
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Primary sponsor: |
Sun Yat-sen University Cancer Center |
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研究实施负责(组长)单位地址: |
中国广东省广州市越秀区东风东路651号、先烈南路青菜岗21号 |
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Primary sponsor's address: |
No.651 Dongfeng East Road, No.21 Qingcaigang Xianlie South Road, Yuexiu District, Guangzhou, Guangdong, China |
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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: |
自选课题(自筹) |
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Source(s) of funding: |
Self-selected Project (Self-financed) |
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研究疾病: |
弥漫大B细胞淋巴瘤 |
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Target disease: |
Diffuse large B‑cell lymphoma |
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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: |
队列研究 |
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Study design: |
Cohort study |
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研究目的: |
1、疗效假设:在真实世界广泛人群中,Hi-CHOP 方案(泽贝妥单抗 + CHOP)治疗初治 CD20 阳性 DLBCL 的 5 年 OS率非劣于 R-CHOP 方案,且可能展现更优的长期无进展生存获益; 2、安全性假设:Hi-CHOP 方案的长期不良事件(AE)、严重不良事件(SAE)发生率及严重程度分布,与 R-CHOP 方案具有可比性,无新增远期安全性风险; 3、亚组假设:在不同预后分层人群(如 IPI 评分、年龄、合并症状态)中,Hi-CHOP 方案的长期疗效与安全性优势 / 非劣效性保持一致。 |
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Objectives of Study: |
1.Efficacy HypothesisIn a broad real-world population, the 5-year overall survival (OS) rate of the Hi-CHOP regimen (Zercepac® plus CHOP) for previously untreated CD20-positive diffuse large B-cell lymphoma (DLBCL) is non-inferior to that of the R-CHOP regimen, and may demonstrate superior long-term progression-free survival benefits. 2.Safety HypothesisThe incidence rate and severity distribution of long-term adverse events (AEs) and serious adverse events (SAEs) associated with the Hi-CHOP regimen are comparable to those of the R-CHOP regimen, with no additional long-term safety risks. 3.Subgroup HypothesisThe consistent long-term efficacy advantages / non-inferiority and safety profile of the Hi-CHOP regimen are maintained across patient subgroups with different prognostic stratifications (e.g., IPI score, age, comorbidity status). |
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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.人口学信息、用药信息关键数据缺失; |
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Exclusion criteria: |
1.Key data on demographic information and medication information are missing. |
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研究实施时间: Study execute time: |
从 From 2026-02-10 00:00:00至 To 2027-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-05-19 00:00:00 至 To 2027-12-31 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: |
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: |
电子采集和管理系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Electronic Data Capture |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |