沉默PD-L1的新型DC疫苗联合CIK治疗胃癌术后病人的随机对照Ⅱ期临床试验

注册号:

Registration number:

ChiCTR1800015690 

最近更新日期:

Date of Last Refreshed on:

2018-04-21 22:36:19 

注册时间:

Date of Registration:

2018-04-18 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

沉默PD-L1的新型DC疫苗联合CIK治疗胃癌术后病人的随机对照Ⅱ期临床试验

Public title:

A randomized controlled phase II clinical trial of a novel DC vaccine silencing PD-L1 combined with CIK for postoperative gastric cancer patients

注册题目简写:

English Acronym:

研究课题的正式科学名称:

沉默PD-L1的新型DC疫苗联合CIK治疗胃癌术后病人的随机对照Ⅱ期临床试验

Scientific title:

A randomized controlled phase II clinical trial of a novel DC vaccine silencing PD-L1 combined with CIK for postoperative gastric cancer patients

研究课题代号(代码):

Study subject ID:

国家国际科技合作专项项目(No. 2015DFA31650)

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:

李玉民 

研究负责人:

李玉民 

Applicant:

Yu-min Li 

Study leader:

Yu-min Li 

申请注册联系人电话:

Applicant telephone:

+86 13893615421

研究负责人电话:

Study leader's
telephone:

+86 13893615421

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:

liym@lzu.edu.cn

研究负责人电子邮件:

Study leader's E-mail:

liym@lzu.edu.cn

申请单位网址(自愿提供):

Applicant website(voluntary supply):

http://www.ldey.cn/Item/1171.aspx

研究负责人网址(自愿提供):

Study leader's website(voluntary supply):

http://www.lzu.edu.cn/v2013/leader/liyumin.html

申请注册联系人通讯地址:

甘肃省兰州市城关区萃英门82号

研究负责人通讯地址:

甘肃省兰州市城关区天水南路222号

Applicant address:

82 Cuiyingmen, Chengguan District, Lanzhou, Gansu, China

Study leader's address:

222 Tianshui Road South, Chengguan District, Lanzhou, Gansu, China

申请注册联系人邮政编码:

Applicant postcode:

730030

研究负责人邮政编码:

Study leader's postcode:

730030

申请人所在单位:

兰州大学第二医院

Applicant's institution:

Lanzhou University Second Hospital

研究负责人所在单位:

兰州大学

Affiliation of the Leader:

Lanzhou 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:

2017A-044

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:

兰州大学第二医院医学伦理委员会

Name of the ethic committee:

Medical Ethics Committee of Lanzhou University Second Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2017-06-22 00:00:00

伦理委员会联系人:

焦作义

Contact Name of the ethic committee:

Zuo-yi Jiao

伦理委员会联系地址:

甘肃省兰州市城关区萃英门82号

Contact Address of the ethic committee:

82 Cuiyingmen, Chengguan District, Lanzhou 730030, Gansu, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

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:

兰州大学

Primary sponsor:

Lanzhou University

研究实施负责(组长)单位地址:

甘肃省兰州市城关区天水南路222号

Primary sponsor's address:

222 South Tianshui Road, Chengguan District, Lanzhou 730030, Gansu, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

甘肃

市(区县):

兰州

Country:

China

Province:

Gansu

City:

Lanzhou

单位(医院):

兰州大学第二医院

具体地址:

甘肃省兰州市城关区萃英门82号 Institution hospital:

Institution
hospital:

Lanzhou University Second Hospital

Address:

82 Cuiyingmen, Chengguan District, Lanzhou 730030, Gansu, China

经费或物资来源:

国家国际科技合作专项项目(No. 2015DFA31650)

Source(s) of funding:

International S&T Cooperation Program of China (No. 2015DFA31650)

研究疾病:

胃癌  

Target disease:

Gastric cancer

研究疾病代码:

C16.9

Target disease code:

C16.9

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

II期临床试验 

Study phase:

2

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

①评估沉默PD-L1的新型DC疫苗联合CIK治疗胃癌术后患者的疗效。 ②建立标准化的胃癌DC疫苗生产流程及临床疗效评价体系,制定应用规范和行业标准。  

Objectives of Study:

1. Evaluate the efficacy of a novel DC vaccine silencing PD-L1 combined with CIK for postoperative gastric cancer patients; 2. Establish a standardized production process and clinical efficacy evaluation system of gastric cancer DC vaccine , draw up the application standards and industry standards.

药物成份或治疗方案详述:

药物成分:沉默PD-L1并负载胃癌全抗原的DC疫苗,CIK 治疗方案:胃癌术后,常规放化疗结束或不能耐受放化疗的患者,给予DC疫苗治疗 

Description for medicine or protocol of treatment in detail:

Description for medicine: A DC vaccine silenced PD-L1 and loaded with full gastric cancer antigen, CIK Protocol of treatment: Patients with gastric cancer, post-operation, completed the conventional radiotherapy and chemotherapy, or not tolerate radiotherapy and chemotherapy, treated with DC vaccine. 

纳入标准:

Inclusion criteria

排除标准:

1.T细胞淋巴瘤患者;
2.严重过敏体质者,尤其是细胞因子IL-2过敏患者;
3.HIV感染者;
4.急性感染者,及严重感染未控制或高热患者;
5.严重免疫缺陷疾病或自身免疫性疾病患者;
6.曾进行骨髓、干细胞或器官移植者;
7.正在使用免疫抑制药物,或器官移植后长期使用免疫抑制剂的患者;
8.脏器功能不全及近期心肌梗塞史(3个月内)患者;
9.严重凝血功能异常者;
10.妊娠或哺乳期妇女;
11.精神病患者及严重抑郁症,以及可能影响其知情同意能力的精神性或成瘾性疾病患者;
12.无法获得免疫状况及进行临床随访评价的患者,以及依从性差的患者;
13.其他研究者认为不适合入组者。

Exclusion criteria:

1. T-cell lymphoma;
2. Those with severe allergic constitution, especially those with cytokine IL-2 allergy;
3. HIV-infected persons;
4. Acute infection, severe infection with uncontrolled or high fever;
5. Patients with severe immunodeficiency or autoimmune diseases;
6. Persons who have undergone bone marrow, stem cell or organ transplantation;
7. Patients who are using immunosuppressive drugs or who have been using immunosuppressants for a long period of time after organ transplantation;
8. patients with organ dysfunction and recent history of myocardial infarction (within 3 months);
9. Severe abnormal coagulation;
10. Pregnant or lactating women;
11. Persons with mental illness and severe depression, as well as persons with mental or addictive diseases that may affect their ability to give informed consent;
12. Patients without access to immunity and clinical follow-up evaluation, as well as patients with poor compliance;
13. Other researchers did not consider it appropriate to join the group.

研究实施时间:

Study execute time:

From 2018-05-01 00:00:00 To 2021-04-30 00:00:00  

征募观察对象时间:

Recruiting time:

From 2018-06-01 00:00:00 To 2020-05-31 00:00:00

干预措施:

Interventions:

组别:

A组

样本量:

38

Group:

A

Sample size:

干预措施:

PD-L1沉默DC-CIK

干预措施代码:

Intervention:

DC-CIK with PD-L1 silenced

Intervention code:

组别:

B组

样本量:

38

Group:

B

Sample size:

干预措施:

普通DC-CIK

干预措施代码:

Intervention:

Ordinary DC-CIK

Intervention code:

组别:

C组

样本量:

38

Group:

C

Sample size:

干预措施:

常规治疗

干预措施代码:

Intervention:

General treatment

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

甘肃 

市(区县):

兰州 

Country:

China

Province:

Gansu

City:

Lanzhou

单位(医院):

兰州大学第二医院 

单位级别:

三级甲等医院 

Institution
hospital:

Lanzhou University Second Hospital ?

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

甘肃 

市(区县):

兰州 

Country:

China

Province:

Gansu

City:

Lanzhou

单位(医院):

兰州军区总医院 

单位级别:

三级甲等医院 

Institution
hospital:

Lanzhou Military General Hospital

Level of the institution:

Tertiary A Hospital

测量指标:

Outcomes:

指标中文名:

树突状细胞表面标志

指标类型:

主要指标

Outcome:

Dendritic cell surface markers

Type:

Primary indicator

测量时间点:

转染沉默前后,树突状细胞成熟时

测量方法:

流式细胞计数

Measure time point of outcome:

Before or after silencing, Dendritic cell maturation;

Measure method:

FCM

指标中文名:

CIK表面标志

指标类型:

主要指标

Outcome:

CIK surface markers

Type:

Primary indicator

测量时间点:

CIK回输前

测量方法:

流式细胞计数

Measure time point of outcome:

Before CIK transfusion

Measure method:

FCM

指标中文名:

DC-CIK功能检测

指标类型:

主要指标

Outcome:

DC-CIK function detection

Type:

Primary indicator

测量时间点:

DC-CIK回输前

测量方法:

酶联免疫吸附试验

Measure time point of outcome:

Before DC-CIK transfusion

Measure method:

ELISA

指标中文名:

KPS评分

指标类型:

主要指标

Outcome:

KPS score

Type:

Primary indicator

测量时间点:

治疗前,治疗后d3,d28,以后半年内每2个月随访一次,半年后每6个月随访一次

测量方法:

体检

Measure time point of outcome:

pre-treatment, post-treatment d3, d28, then every 2-month during the first half year, every 6-month after half year

Measure method:

physical examination

指标中文名:

血、尿、粪常规,肝、肾功,凝血功能

指标类型:

次要指标

Outcome:

Blood, urine, fecal routine, liver, renal function, coagulation function

Type:

Secondary indicator

测量时间点:

治疗前,治疗后d3,d28,以后半年内每2个月随访一次,半年后每6个月随访一次

测量方法:

血清、尿液、粪便

Measure time point of outcome:

pre-treatment, post-treatment d3, d28, then every 2-month during the first half year, every 6-month after half year

Measure method:

serum, urine, feces

指标中文名:

肿瘤病灶评估

指标类型:

主要指标

Outcome:

Tumor lesions assessment

Type:

Primary indicator

测量时间点:

治疗前,治疗后d3,d28,以后半年内每2个月随访一次,半年后每6个月随访一次

测量方法:

体检,影像,胃镜

Measure time point of outcome:

pre-treatment, post-treatment d3, d28, then every 2-month during the first half year, every 6-month after half year

Measure method:

physical examination, imageology, gastroscopy

指标中文名:

外周血淋巴细胞亚群

指标类型:

主要指标

Outcome:

Peripheral blood lymphocyte subsets

Type:

Primary indicator

测量时间点:

治疗前,治疗后d3,d28,以后半年内每2个月随访一次,半年后每6个月随访一次

测量方法:

流式细胞计数

Measure time point of outcome:

pre-treatment, post-treatment d3, d28, then every 2-month during the first half year, every 6-month after half year

Measure method:

FCM

指标中文名:

血浆细胞因子

指标类型:

主要指标

Outcome:

Plasma cytokines

Type:

Primary indicator

测量时间点:

治疗前,治疗后d3,d28,以后半年内每2个月随访一次,半年后每6个月随访一次

测量方法:

酶联免疫吸附试验

Measure time point of outcome:

pre-treatment, post-treatment d3, d28, then every 2-month during the first half year, every 6-month after half year

Measure method:

ELISA

指标中文名:

肿瘤标志物

指标类型:

主要指标

Outcome:

Tumor markers

Type:

Primary indicator

测量时间点:

治疗前,治疗后d3,d28,以后半年内每2个月随访一次,半年后每6个月随访一次

测量方法:

血清

Measure time point of outcome:

pre-treatment, post-treatment d3, d28, then every 2-month during the first half year, every 6-month after half year

Measure method:

serum

指标中文名:

淋巴细胞功能试验

指标类型:

主要指标

Outcome:

Lymphocyte function test

Type:

Primary indicator

测量时间点:

治疗前,治疗后d28

测量方法:

患者外周血单个核细胞

Measure time point of outcome:

pre-treatment, post-treatment d28

Measure method:

peripheral blood mononuclear cell of patients

指标中文名:

生存率和生存期

指标类型:

主要指标

Outcome:

Survival rate and survival time

Type:

Primary indicator

测量时间点:

治疗后6个月、1年、18个月、2年、3年、5年

测量方法:

生存分析

Measure time point of outcome:

6-moth, 1-year, 18-month, 2-year, 3-year, 5-year post-treatment

Measure method:

survive analysis

指标中文名:

安全性评价

指标类型:

主要指标

Outcome:

safety evaluation

Type:

Primary indicator

测量时间点:

治疗后d3,d28,以后半年内每2个月随访一次,半年后每6个月随访一次

测量方法:

不良反应

Measure time point of outcome:

post-treatment d3, d28, then every 2-month during the first half year, every 6-month after half year

Measure method:

adverse reactions

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

血液

组织:

血液

Sample Name:

blood

Tissue:

blood

人体标本去向

使用后保存  

说明

提取细胞

Fate of sample:

Preservation after use  

Note:

extract cells

标本中文名:

胃癌标本

组织:

Sample Name:

gastric cancer specimens

Tissue:

gastric

人体标本去向

使用后保存  

说明

提取细胞

Fate of sample:

Preservation after use  

Note:

extract cells

征募研究对象情况:

Recruiting status:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 80 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):

由随机分组设计者用SPSS软件生成随机数字,把1-114号数字随机分为A、B、C组,每组38例,分别单独装入顺序编号、不透明、密封的信封,一式4份,随机分组设计者、课题负责人、临床医生、数据管理者各保留一份。随机分组设计者不参与后期的实验研究。

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

The random group designer used SPSS software to generate random numbers. The number 1-114 was randomly divided into A,B,C groups. 38 patients in each group were individually loaded with sequential numbered, opaque and sealed envelopes, and 4 copies were assigned. Group designers, project man

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:

对数据收集和数据分析者施盲

Blinding:

Blind to data collector and data analyst.

试验完成后的统计结果(上传文件):

Calculated Results after
the Study Completed(upload file):

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):

原始数据会在2021年10月31日之前上传至ResMan系统。

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

The data will be uploaded to ResMane and accessible to public before October 31, 2021.

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:

采用病例记录表记录数据,Excel汇总整理。

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

The data will be managed by case record form and collected by Excel.

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2018-04-15 21:35:46