|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR2200060450 |
|
最近更新日期: Date of Last Refreshed on: |
2022-07-15 10:49:50 |
|
注册时间: Date of Registration: |
2022-06-01 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
基于循环肿瘤DNA动态监控中国外周T细胞淋巴瘤(PTCL)患者疗效研究 |
|
Public title: |
Dynamic monitoring of peripheral T-cell lymphoma (PTCL) patients in China based on circulating tumor DNA |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
基于循环肿瘤DNA动态监控中国外周T细胞淋巴瘤(PTCL)患者疗效研究 |
|
Scientific title: |
Dynamic monitoring of peripheral T-cell lymphoma (PTCL) patients in China based on circulating tumor DNA |
|
研究课题代号(代码): Study subject ID: |
|
|
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: |
|
申请注册联系人: |
刘科宇 |
研究负责人: |
马军 |
|
Applicant: |
Keyu Liu |
Study leader: |
Ma Jun |
|
申请注册联系人电话: Applicant telephone: |
+86 451-87672631 |
研究负责人电话:
Study leader's |
+86 13304518000 |
|
申请注册联系人传真 : Applicant Fax: |
+86 451-87672631 |
研究负责人传真: Study leader's fax: |
+86 0451-87650339 |
|
申请注册联系人电子邮件: Applicant E-mail: |
gesiza@163.com |
研究负责人电子邮件: Study leader's E-mail: |
mjun0322@126.com |
|
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): |
||
|
申请注册联系人通讯地址: |
黑龙江省哈尔滨市道里区地段街149号 |
研究负责人通讯地址: |
黑龙江省哈尔滨市道里区地段街149号 |
|
Applicant address: |
149 Diduan Street, Daoli District, Harbin, Heilongjiang, China |
Study leader's address: |
149 Diduan Street, Daoli District, Harbin, Heilongjiang |
|
申请注册联系人邮政编码: Applicant postcode: |
150010 |
研究负责人邮政编码: Study leader's postcode: |
150010 |
|
申请人所在单位: |
哈尔滨市第一医院 |
||
|
Applicant's institution: |
Harbin First Hospital |
||
|
研究负责人所在单位: |
|
||
|
Affiliation of the Leader: |
|
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
IIT2022-001 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
|
批准本研究的伦理委员会名称: |
哈尔滨市第一医院血液肿瘤研究中心伦理委员会 |
||
|
Name of the ethic committee: |
Ethics Committee of Hematological Tumor Research Center of Harbin The First Hospital |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2022-07-07 00:00:00 | ||
|
伦理委员会联系人: |
程梅 |
||
|
Contact Name of the ethic committee: |
Cheng Mei |
||
|
伦理委员会联系地址: |
黑龙江省哈尔滨市道里区地段街149号 |
||
|
Contact Address of the ethic committee: |
149 Diduan Street, Daoli District, Harbin, Heilongjiang |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
0451-84883432 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
|
|
研究实施负责(组长)单位: |
哈尔滨市第一医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Harbin First Hospital |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
黑龙江省哈尔滨市道里区地段街151号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
151 Diduan Street, Daoli District, Harbin, Heilongjiang |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
北京橡鑫生物科技有限公司 |
||||||||||||||||||||||
|
Source(s) of funding: |
Beijing AcornMed Biotechnology Co., Ltd. |
||||||||||||||||||||||
|
研究疾病: |
外周T细胞淋巴瘤 |
||||||||||||||||||||||
|
Target disease: |
Peripheral T-cell lymphoma |
||||||||||||||||||||||
|
研究疾病代码: |
|
||||||||||||||||||||||
|
Target disease code: |
|
||||||||||||||||||||||
|
研究类型: |
观察性研究 |
||||||||||||||||||||||
|
Study type: |
Observational study |
||||||||||||||||||||||
|
研究所处阶段: |
探索性研究/预试验 | ||||||||||||||||||||||
|
Study phase: |
0 |
||||||||||||||||||||||
|
研究设计: |
连续入组 |
||||||||||||||||||||||
|
Study design: |
Sequential |
||||||||||||||||||||||
|
研究目的: |
(1)主要目的:PTCL患者基线时期、4周期治疗后和治疗完全结束后ctDNA浓度动态变化与终期疗效相关性分析,探索ctDNA作为疗效监测指标的可行性。 (2)次要目的:PTCL患者诊断时期组织DNA与外周血ctDNA在检出突变位点的一致性分析与符合率分析;PTCL患者诊断时期外周血ctDNA浓度与PET-CT TMTV肿瘤负荷的相关性分析;PTCL患者初诊时期基线突变图谱绘制,建立PTCL患者基因突变数据库;关联分析CD30表达情况与PTCL患者的疗效。 |
||||||||||||||||||||||
|
Objectives of Study: |
(1) Primary objective: Explore the feasibility of ctDNA as a therapeutic effect monitoring indicator based on the correlation between the dynamic changes of ctDNA concentration at baseline, after 4 cycles of treatment and after complete treatment and the terminal efficacy of PTCL patients. (2) Secondary objective: Analyse the consistency and coincidence rate of tissue DNA and ctDNA in peripheral blood in PTCL patients at diagnosis; Correlate analysis between ctDNA concentration in peripheral blood and tumor load of PET-CT TMTV at diagnosis in PTCL patients; Draw the mutation map of PTCL patients at diagnosis, and establish the gene mutation database of PTCL patients; Correlate analysis of CD30 expression and efficacy of PTCL patients. |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
本研究不涉及试验用药 |
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
This study does not involve trial medication |
||||||||||||||||||||||
|
纳入标准: |
(1)根据2016 WHO造血和淋巴组织肿瘤分类,组织病理确诊为初诊PTCL患者; |
||||||||||||||||||||||
|
Inclusion criteria |
(1)According to the 2016 WHO Classification of hematopoietic and lymphoid tumors, the histopathological diagnosis is confirmed as a newly diagnosed PTCL patient; |
||||||||||||||||||||||
|
排除标准: |
(1)以前或目前患有其他恶性血液肿瘤; |
||||||||||||||||||||||
|
Exclusion criteria: |
(1)Patient with a previous or current history of other hematologic malignancies; |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2022-05-31 00:00:00至 To 2024-04-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2022-05-31 00:00:00 至 To 2023-07-31 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
|
||||||
|
性别: |
男女均可 |
Gender: |
Both |
||||||
|
随机方法(请说明由何人用什么方法产生随机序列): |
不适用 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
N/A |
||||||||
|
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 |
|
盲法: |
|
|
Blinding: |
|
是否共享原始数据: IPD sharing |
否No |
|
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): |
不共享 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Not shared |
|
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: |
不共享 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Not shared |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |