|
注册号: Registration number: |
ChiCTR1900021395 |
|
最近更新日期: Date of Last Refreshed on: |
2019-02-24 17:39:41 |
|
注册时间: Date of Registration: |
2019-02-18 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
非小细胞肺癌免疫状态及免疫疗效评估 |
|
Public title: |
Molecular characterization of clinical responses to PD-1/PD-L1 inhibition in non-small cell lung cancer |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
非小细胞肺癌免疫状态及免疫疗效评估 |
|
Scientific title: |
Molecular characterization of clinical responses to PD-1/PD-L1 inhibition in non-small cell lung cancer |
|
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: |
王建飞 |
研究负责人: |
白春学 洪群英 |
|
Applicant: |
Jianfei Wang |
Study leader: |
Chunxue Bai,Qunying Hong |
|
申请注册联系人电话: Applicant telephone: |
+86 15910397982 |
研究负责人电话:
Study leader's |
+86 18621170011; 13816880830 |
|
申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
+86 021 64187165 | |
|
申请注册联系人电子邮件: Applicant E-mail: |
wangjianfei@gloriousmed.com |
研究负责人电子邮件: Study leader's E-mail: |
qyhong68@hotmail.com |
|
申请单位网址(自愿提供): Applicant website(voluntary supply): |
https://www.gloriousmed.com |
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: |
北京市朝阳区南湖东园122号博泰国际B座1009室 |
研究负责人通讯地址: |
上海市徐汇区枫林路180号 |
|
Applicant address: |
Room 1009, Botai international Building B, 122 Nanhu Park East, Wangjing Street, Chaoyang District, Beijing, China |
Study leader's address: |
180 Fenglin Road, Xuhui District, Shanghai, China |
|
申请注册联系人邮政编码: Applicant postcode: |
100102 |
研究负责人邮政编码: Study leader's postcode: |
|
|
申请人所在单位: |
上海仁东医学检验所有限公司 |
||
|
Applicant's institution: |
GloriousMed Technology Co.,Ltd. |
||
|
研究负责人所在单位: |
复旦大学附属中山医院 |
||
|
Affiliation of the Leader: |
Zhongshan Hospital Fudan University |
||
|
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: |
B2018-284R |
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: |
复旦大学附属中山医院伦理委员会 |
||
|
Name of the ethic committee: |
Ethics committee of zhongshan hospital fudan university |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2018-12-28 00:00:00 | ||
|
伦理委员会联系人: |
复旦大学附属中山医院 |
||
|
Contact Name of the ethic committee: |
Zhongshan Hospital, Fudan University |
||
|
伦理委员会联系地址: |
上海市徐汇区枫林路180号 |
||
|
Contact Address of the ethic committee: |
180 Fenglin Road, Xuhui District, Shanghai, China |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 021 64041990-3257 |
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: |
复旦大学附属中山医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Zhongshan Hospital, Fudan University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
上海市徐汇区枫林路180号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
180 Fenglin Road, Xuhui District, Shanghai, China |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
上海仁东医学检验所有限公司 |
||||||||||||||||||||||
|
Source(s) of funding: |
GloriousMed Technology Co.,Ltd. |
||||||||||||||||||||||
|
研究疾病: |
非小细胞肺癌 |
||||||||||||||||||||||
|
Target disease: |
NSCLC |
||||||||||||||||||||||
|
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: |
通过本前瞻性观察研究,完成大样本检测/临床数据的积累,确立非小细胞肺癌患者PD-1/PD-L1抑制剂疗效相关生物标志物及其cut-off值,从而构建综合预测模型。其次进行免疫疗效探索分析,分析不同突变类型(SNV/Indel/CNV)的数量/占比对于免疫治疗的影响;验证已知的DNA修复相关基因/免疫治疗耐药/超进展进行基因与免疫治疗之间的关系。同时进行免疫治疗液体活检探索,基于ctDNA技术来分析治疗前外周血的TMB,用以预测免疫治疗的疗效;比较治疗前后ctDNA中突变谱的变化,用以分析免疫治疗的疗效,鉴别假进展以及提前预知耐药/进展。 |
||||||||||||||||||||||
|
Objectives of Study: |
The main purposes of this prospective observational study are to accumulate large and complete samples and clinical data, to verify the biomarkers and their cut-off values related to the efficacy of PD-1/PD-L1 inhibitors in Chinese NSCLC patients, and to construct a comprehensive predictive model from those data. The secondary purposes are to explore the relationship between numbers and/or frequencies of certain genetic variations (SNVs/Indels/CNVs) and immunotherapy response, and to verify the influence of known DNA repair-related genes on immunotherapy resistance and /or hyper-progression disease. This study will also focus on application of liquid biopsy, especially the mutation spectrum and TMB in circulating tumor DNA (ctDNA), in discriminating pseudo-progression and predicting resistance or progression of immunotherapy. |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||
|
纳入标准: |
|||||||||||||||||||||||
|
Inclusion criteria |
|||||||||||||||||||||||
|
排除标准: |
(1) 入组前14天内或研究期间需要接受全身用皮质类固醇(剂量相当于或高于10mg/天强的松)或其他免疫抑制药物治疗的受试者; |
||||||||||||||||||||||
|
Exclusion criteria: |
1. Subjects who need to receive systemic corticosteroid (equivalent to or higher than 10mg/ day prednisone) or other immunosuppressive drugs within 14 days before enrollment or during the study period; |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2018-11-30 00:00:00至 To 2020-03-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2019-03-31 00:00:00 至 To 2019-09-30 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): |
无 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
No |
||||||||
|
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 |
|
盲法: |
Open |
|
Blinding: |
Open |
|
试验完成后的统计结果(上传文件): |
|
|
Calculated Results after
|
|
|
是否共享原始数据: IPD sharing |
是Yes |
|
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): |
各中心项目结束后,数据分析完毕即各中心负责人均可拿到分析结果 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
After the end of each center project, the data analysis is completed, which means that the person in charge of each center can get the analysis results |
|
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: |
本研究设置了CRF表,会在每个实施医院派专人负责CRF表信息的搜集。 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
In this study, CRF tables were set up, and special personnel were assigned to collect CRF table information in each hospital. |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |