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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2500100336 |
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最近更新日期: Date of Last Refreshed on: |
2025-04-08 09:33:27 |
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注册时间: Date of Registration: |
2025-04-08 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: |
EB病毒相关多种新型标志物在鼻咽癌筛查中的应用评价:一项多中心前瞻性队列研究 |
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Public title: |
Evaluation of multiple novel biomarkers associated with Epstein-Barr virus in nasopharyngeal carcinoma screening: a multicenter prospective cohort study |
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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: |
EB病毒相关多种新型标志物在鼻咽癌筛查中的应用评价:一项多中心前瞻性队列研究 |
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Scientific title: |
Evaluation of multiple novel biomarkers associated with Epstein-Barr virus in nasopharyngeal carcinoma screening: a multicenter prospective cohort study |
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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: |
李彤 |
研究负责人: |
曹素梅 |
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Applicant: |
Li Tong |
Study leader: |
Cao Sumei |
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申请注册联系人电话: Applicant telephone: |
+86 20 8734 5683 |
研究负责人电话: Study leader's telephone: |
+86 20 8734 5685 |
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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: |
litong1@sysucc.org.cn |
研究负责人电子邮件: Study leader's E-mail: |
caosm@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: |
广东省广州市东风东路651号 |
研究负责人通讯地址: |
广东省广州市东风东路651号 |
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Applicant address: |
651 Dongfeng East Road, Guangzhou City, Guangdong Province |
Study leader's address: |
651 Dongfeng East Road, Guangzhou City, Guangdong Province |
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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/Yes |
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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: |
B2025-017-01 |
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 Cancer Center, Sun Yat-sen University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-02-17 00:00:00 |
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伦理委员会联系人: |
陈琼 |
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Contact Name of the ethic committee: |
Chen Qiong |
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伦理委员会联系地址: |
广东省广州市东风东路651号 |
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Contact Address of the ethic committee: |
651 Dongfeng East Road, Guangzhou City, Guangdong Province |
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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: |
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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: |
广东省广州市东风东路651号 |
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Primary sponsor's address: |
651 Dongfeng East Road, Guangzhou City, Guangdong Province |
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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: |
国家科技重大专项课题 |
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Source(s) of funding: |
National Science and Technology Major Project of China |
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Target disease: |
Nasopharyngeal carcinoma |
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Target disease code: |
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研究类型: |
诊断试验 |
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Study type: |
Diagnostic test |
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研究所处阶段: |
诊断试验新技术临床试验 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Study phase: |
Diagnostic New Technique Clincal Study |
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研究设计: |
诊断试验诊断准确性 |
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Study design: |
Diagnostic test for accuracy |
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研究目的: |
通过在4个高发现场开展3.3万人群的多中心前瞻性队列研究,比较应用P85-Ab新型抗体与传统的ELISA双抗体相比,能否提高鼻咽癌筛查的敏感度和特异度;比较采用化学发光技术的双抗体检测较传统的ELISA双抗体的检测效果;比较新型分子指标(E-CpMQ)分流后联合MRI靶向活检策略与单独鼻咽内镜检查策略在抗体初筛阳性人群中检出鼻咽癌效果。在基于卫生经济学评价的基础上,形成30-69岁高发期人群的鼻咽癌筛查的推荐意见。 |
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Objectives of Study: |
A multicenter prospective cohort study involving 33,000 participants across four high-incidence areas will be conducted to compare the performance of the novel P85-Ab antibody with traditional ELISA double antibody assays in terms of improving the sensitivity and specificity of nasopharyngeal carcinoma (NPC) screening. The study will also compare the detection efficacy of the chemiluminescence-based double antibody assay with that of the traditional ELISA double antibody assay. Additionally, it will evaluate the diagnostic effectiveness of a combined strategy using novel molecular markers (E-CpMQ) with MRI-targeted biopsy versus a single nasopharyngoscopy strategy in antibody-positive individuals. Based on health economic evaluation, recommendations for NPC screening in high-risk populations aged 30-69 will be formulated. |
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药物成份或治疗方案详述: |
对所有入组的筛查人群,都采用化学发光法检测其外周血P85-Ab抗体、EBV VCA-IgA及EBNA1-IgA,同时采用ELISA法检测外周血EBV VCA-IgA及EBNA1-IgA。任一生物学指标检测结果阳性,均召回进行鼻咽内镜检查并同时采集左右鼻咽的鼻咽拭子进行E-CpMQ检测。鼻咽内镜检查发现可疑病变(4级)而E-CpMQ检测阴性的受试者,则根据鼻咽内镜的指示取活检进行病理检查。对于所有E-CpMQ检测阳性的受试者全部召回进行MRI检测,若MRI显示可疑病变则根据MRI的指引进行活检;若MRI结果为阴性(1~3级)而鼻咽内镜显示异常,则根据鼻咽内镜的指示取活检进行病理检查。对于MRI提示阳性(4~5级)而病理检查为非鼻咽癌的人群在半年后重新抽血复查,其他高危人群在一年后进行复查。 |
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Description for medicine or protocol of treatment in detail: |
For all enrolled screening participants, chemiluminescence assays will be used to detect serum P85-Ab antibodies, EBV VCA/IgA, and EBNA1/IgA, while ELISA assays will be used to detect serum EBV VCA/IgA and EBNA1/IgA. Any positive result from a above indicator will refer for nasopharyngoscopy, along with the collection of nasopharyngeal swabs from both sides for E-CpMQ detection. Participants with suspicious lesions (Grade 4) found by nasopharyngoscopy but negative E-CpMQ results will undergo biopsy for pathological examination based on the indications of the nasopharyngoscopy. All participants with positive E-CpMQ results will be recalled for MRI scanning, and if MRI shows suspicious lesions, biopsy will be performed according to MRI guidance. If MRI results are negative (Grade 1-3) but nasopharyngoscopy shows abnormalities, biopsy will be performed based on nasopharyngoscopy indications. For individuals with MRI-positive results (Grade 4-5) but negative pathological findings, a follow-up blood test will be conducted six months later, while other high-risk individuals will undergo a follow-up test one year later. |
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纳入标准: |
1) 筛查地区30-69岁的户籍居民; 2) 既往无鼻咽癌病史; 3) ECOG 0-2; 4) 同意签署知情同意书。 |
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Inclusion criteria |
1) Registered residents aged 30-69 in the screening area; 2) No history of nasopharyngeal cancer; 3) ECOG 0-2; 4) The participant agrees to sign the informed consent. |
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排除标准: |
1) 患有心、脑、肝、肺、肾疾病患者; 2) 自身免疫性疾病患者; 3) 目前在接受糖皮质激素或免疫抑制疗法的患者; 4) 精神状态差,意识不清楚。 |
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Exclusion criteria: |
1) Patients with heart, brain, liver, lung and kidney diseases; 2) Patients with autoimmune diseases; 3) Patients currently receiving glucocorticoid or immunosuppressive therapy; 4) People with poor mental state, unclear consciousness. |
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研究实施时间: Study execute time: |
从 From 2025-04-10 00:00:00至 To 2027-12-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2025-04-10 00:00:00 至 To 2026-12-31 00:00:00 |
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诊断试验: Diagnostic Tests: |
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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): |
本研究不进行随机分组 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
This study was not randomized |
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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: |
公开/Public |
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盲法: |
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Blinding: |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
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): |
原始数据不共享 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Raw data is not shared |
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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: |
按照电子CRF表的内容建立数据库,聘请专门的数据管理员进行管理。采用SPSS 20.0对数据资料进行整理分析。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Establish a database according to the contents of the electronic CRF table and hire a special data administrator to manage it. SPSS 20.0 are used to sort out and analyze the data. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |