中国原发性肝癌免疫疗法的安全状况和管理实践评估

注册号:

Registration number:

ChiCTR2400085934 

最近更新日期:

Date of Last Refreshed on:

2024-06-21 10:34:47 

注册时间:

Date of Registration:

2024-06-21 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

中国原发性肝癌免疫疗法的安全状况和管理实践评估

Public title:

Evaluation of Safety Measures and Management Practices for Immunotherapy for Primary Liver Cancer in Chinese Population

注册题目简写:

English Acronym:

研究课题的正式科学名称:

肝胆肿瘤免疫治疗安全性调研

Scientific title:

Safety Study of Immunotherapy for Hepatobiliary Tumors

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:

林志珊 

研究负责人:

徐立; 孙惠川 

Applicant:

Lin Zhishan 

Study leader:

Xu Li; Sun Huichuan 

申请注册联系人电话:

Applicant telephone:

+86 138 2600 6928

研究负责人电话:

Study leader's
telephone:

+86 135 2765 6798

申请注册联系人传真 :

Applicant Fax:

研究负责人传真:

Study leader's fax:

申请注册联系人电子邮件:

Applicant E-mail:

linzhsh@sysucc.org.cn

研究负责人电子邮件:

Study leader's E-mail:

xuli@sysucc.org.cn

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:

广州市越秀区东风东路651号

研究负责人通讯地址:

广州市越秀区东风东路651号; 上海市徐汇区枫林路180号

Applicant address:

Building 1, 651 Dongfeng East Road, Yuexiu District, Guangzhou City

Study leader's address:

No. 651 Dongfeng East Road, Yuexiu District, Guangzhou City; 180 Fenglin Road, Xuhui District, Shanghai

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:

申请人所在单位:

中山大学附属肿瘤医院

Applicant's institution:

Sun Yat-sen University Cancer Center

研究负责人所在单位:

中山大学附属肿瘤医院; 复旦大学附属中山医院

Affiliation of the Leader:

Sun Yat-sen University Cancer Center; Zhongshan Hospital Affiliated to Fudan University

是否获伦理委员会批准:

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

B2021-290-01; B2021-348R

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:

中山大学肿瘤防治中心伦理委员会;复旦大学附属中山医院伦理委员会

Name of the ethic committee:

Ethics Committee of Sun Yat-sen University Cancer Prevention and Treatment Center; Ethics Committee of Zhongshan Hospital Affiliated to Fudan University

伦理委员会批准日期:

Date of approved by ethic committee:

2021-09-22 00:00:00

伦理委员会联系人:

陈琼

Contact Name of the ethic committee:

Chen Qiong

伦理委员会联系地址:

广东省广州市先烈南路23号翠园楼316 室;上海市徐汇区枫林路180号复旦大学附属中山医院5号楼412室

Contact Address of the ethic committee:

Room 316, Cuiyuan Building, No. 23 Xianlie South Road, Guangzhou, Guangdong Province; Room 412, Building 5, Zhongshan Hospital Affiliated to Fudan University, 180 Fenglin Road, Xuhui District, Shanghai

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 20 8734 3009

伦理委员会联系人邮箱:

Contact email of the ethic committee:

llwyh@sysucc.org.cn

研究实施负责(组长)单位:

复旦大学附属中山医院;中山大学附属肿瘤医院

Primary sponsor:

Zhongshan Hospital Affiliated to Fudan University; Sun Yat-sen University Cancer Center

研究实施负责(组长)单位地址:

上海市徐汇区枫林路180号;广州市越秀区东风东路651号

Primary sponsor's address:

180 Fenglin Road, Xuhui District, Shanghai; 651 Dongfeng East Road, Yuexiu District, Guangzhou

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

广东省

市(区县):

Country:

China

Province:

Guangdong Province

City:

单位(医院):

中山大学附属肿瘤医院

具体地址:

广州市越秀区东风东路651号

Institution
hospital:

Sun Yat-sen University Cancer Center

Address:

No. 651 Dongfeng East Road, Yuexiu District, Guangzhou City

国家:

中国

省(直辖市):

上海市

市(区县):

Country:

China

Province:

Shanghai

City:

单位(医院):

复旦大学附属中山医院

具体地址:

上海市徐汇区枫林路180号

Institution
hospital:

Zhongshan Hospital Affiliated to Fudan University

Address:

180 Fenglin Road, Xuhui District, Shanghai

经费或物资来源:

Source(s) of funding:

None

研究疾病:

肝胆恶性肿瘤  

Target disease:

Hepatobiliary Malignancies

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:

回顾性研究 

Study phase:

Retrospective study

研究设计:

连续入组 

Study design:

Sequential 

研究目的:

本次调研的目的在于通过收集肝胆肿瘤患者在接受 PD-1/PD-L1 免疫治疗药物治疗后的不良反应发生情况、患者生活质量及其影响因素等信息,从肿瘤患者的角度出发,关注其身体健康、心理健康和社会适应性等。  

Objectives of Study:

The purpose of this survey is to collect information on the incidence of adverse reactions, quality of life, and influencing factors of liver and gallbladder tumor patients after receiving PD-1/PD-L1 immunotherapy drugs. From the perspective of tumor patients, attention is paid to their physical health, psychological health, and social adaptability.

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. 正在参加其他PD-1/PD-L1 药物的临床试验 2. 医生判断理解力或依从性不佳,不适合参加本次调研

Exclusion criteria:

1. Currently participating in clinical trials of other PD-1/PD-L1 drugs 2. Judged by doctors to have poor understanding or compliance, and not suitable for participating in this survey

研究实施时间:

Study execute time:

From 2022-05-06 00:00:00 To 2025-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-05-06 00:00:00 To 2025-12-31 00:00:00

干预措施:

Interventions:

组别:

连续入组(第一部分)

样本量:

1100

Group:

Case series (Part 1)

Sample size:

干预措施:

干预措施代码:

Intervention:

N/A

Intervention code:

组别:

连续入组(第二部分)

样本量:

300

Group:

Case series (Part 2)

Sample size:

干预措施:

干预措施代码:

Intervention:

N/A

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

广东省 

市(区县):

 

Country:

China

Province:

Guangdong Province

City:

单位(医院):

中山大学附属肿瘤医院 

单位级别:

三甲 

Institution
hospital:

Sun Yat-sen University Cancer Center

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

上海 

市(区县):

 

Country:

China

Province:

Shanghai

City:

单位(医院):

复旦大学附属中山医院 

单位级别:

三甲 

Institution
hospital:

Zhongshan Hospital Affiliated to Fudan University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

不良反应评估量表

指标类型:

主要指标

Outcome:

Adverse reaction assessment scale

Type:

Primary indicator

测量时间点:

测量方法:

问卷调查法

Measure time point of outcome:

Measure method:

Questionnaire Survey Method

指标中文名:

生活质量评估量表(EORTC QLQ-C30)

指标类型:

主要指标

Outcome:

Quality of Life Assessment Scale (EORTC QLQ-C30)

Type:

Primary indicator

测量时间点:

测量方法:

问卷调查法

Measure time point of outcome:

Measure method:

Questionnaire Survey Method

指标中文名:

中国患者免疫治疗特异性问卷

指标类型:

次要指标

Outcome:

Chinese Patient Immunotherapy Specific Questionnaire

Type:

Secondary indicator

测量时间点:

测量方法:

问卷调查法

Measure time point of outcome:

Measure method:

Questionnaire Survey Method

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

组织:

Sample Name:

None

Tissue:

None

人体标本去向

其它  

说明

Fate of sample:

0thers  

Note:

None

征募研究对象情况:

Recruiting status:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age years

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):

Randomization Procedure (please state who generates the random number sequence and by what method):

None

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):

文章发表后原始数据将上传到 Research Data Deposit(RDD网站),网址 www.researchdata.org.cn

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

After publication, the raw data will be uploaded to Research Data Deposit (www.researchdata.org.cn)

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:

本调研采用线上问卷分发和回收方式进行数据的采集

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

This survey adopts the form of online questionnaire distribution and collection for data collection

数据与安全监察委员会:

Data and Safety Monitoring Committee:

暂未确定/Not yet

注册人:

Name of Registration:

 2024-06-21 10:34:44