Peripheral Blood CyTOF Immune Model for Cervical Lesion Detection in HPV16/18+ Women
2026年5月18日 更新者:Wang Hui、Women's Hospital School Of Medicine Zhejiang University
Mass Cytometry-based Peripheral Blood Immune Model for Accurate Detection of Cervical Lesions in HPV16/18-positive Women: a Multicenter Study
This prospective, multicenter cohort study will recruit eligible HPV16/18-positive women from three tertiary hospitals in China.
Peripheral blood samples and clinical data (cytology, HPV genotyping, colposcopy-directed biopsy) will be collected, followed by standardized mass cytometry (CyTOF) to develop and evaluate an immune model across cervical lesion grades.
研究概览
地位
尚未招聘
详细说明
This study aimed to validate the diagnostic efficacy of our previously established CyTOF-based immune model for identifying CIN3+ lesions (including CIN3 and cervical cancer) in a multicenter prospective cohort of HPV16/18-positive women.
In addition, this study seeks to promote the standardized implementation of mass cytometry in cervical lesion triage, construct a non-invasive, high-throughput and high-accuracy immune diagnostic workflow, improve the diagnostic efficiency and precision management of HPV16/18-positive populations, and minimize unnecessary invasive examinations as well as patients' psychological burden.
Ultimately, it is expected to advance the precision-oriented optimization of national cervical cancer prevention strategies.
Meanwhile, the feasibility and clinical superiority of this model will be evaluated by comparing it with current mainstream screening modalities, such as cervical cytology, HPV genotyping and colposcopy-guided cervical biopsy, which lays a solid foundation for the subsequent development of related auxiliary diagnostic reagents and products.(1)Primary
objective: To validate the diagnostic efficacy (sensitivity, specificity, area under the curve [AUC]) of the CyTOF-based immune model for detecting CIN3+ lesions in HPV16/18-positive women.(2)Secondary
objective: To validate the diagnostic efficacy (sensitivity, specificity, AUC) of the CyTOF-based immune model for detecting CIN2+ lesions in HPV16/18-positive women, and to compare its accuracy, positive and negative predictive values with those of conventional screening methods (including cytology, HPV genotyping, and colposcopy-directed cervical biopsy).
(3)Exploratory objective: To investigate the adaptability and stability of the model across different populations (e.g., by age group and vaccination status).
研究类型
观察性的
注册 (估计的)
1465
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Junfen Xu
- 电话号码:+86 13567147767
- 邮箱:xjfzu@zju.edu.cn
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
取样方法
非概率样本
研究人群
HPV16/18-positive patients
描述
Inclusion Criteria:
- Availability of cervical cytology results
- Consent to colposcopy and cervical biopsy
- Signed informed consent
Exclusion Criteria:
- Confirmed diagnosis of CIN2 or worse
- Prior cervical ablation, cervical conization, chemoradiotherapy, or immunotherapy
- Other malignancy within the past 2 years not in complete remission
- Presence of other systemic immune disease or active infection
- Pregnancy or lactation
- Inability to comply with follow-up and examinations
- Inability to comply with study procedures, restrictions, and requirements, as determined by the investigator
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
The diagnostic sensitivity of the CyTOF-based immune model for detecting CIN3+ lesions in HPV16/18-positive women
大体时间:through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
|
AUC of the CyTOF-based immune model for detecting CIN3+ lesions in HPV16/18-positive women
大体时间:through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
|
The diagnostic specificity of the CyTOF-based immune model for detecting CIN3+ lesions in HPV16/18-positive women
大体时间:through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
The diagnostic sensitivity of the CyTOF-based immune model for detecting CIN2+ lesions in HPV16/18-positive women,
大体时间:through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
|
AUC of the CyTOF-based immune model for detecting CIN2+ lesions in HPV16/18-positive women
大体时间:through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
|
The diagnostic specificity of the CyTOF-based immune model for detecting CIN2+ lesions in HPV16/18-positive women
大体时间:through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
|
Compare the CyTOF-based immune model's accuracy with those of conventional screening methods (including cytology, HPV genotyping, and colposcopy-directed cervical biopsy)
大体时间:through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
|
Compare the CyTOF-based immune model's positive predictive values with those of conventional screening methods (including cytology, HPV genotyping, and colposcopy-directed cervical biopsy)
大体时间:through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
|
Compare the CyTOF-based immune model's negative predictive values with those of conventional screening methods (including cytology, HPV genotyping, and colposcopy-directed cervical biopsy)
大体时间:through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
|
AUC of the CyTOF-based immune model for detecting CIN3+ lesions across subgroups(e.g., by age group and vaccination status)
大体时间:through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
|
Calibration Slope of the CyTOF-based immune model for detecting CIN3+ lesions across subgroups (e.g., by age group and vaccination status)
大体时间:through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年5月15日
初级完成 (估计的)
2027年3月31日
研究完成 (估计的)
2028年3月31日
研究注册日期
首次提交
2026年5月6日
首先提交符合 QC 标准的
2026年5月18日
首次发布 (实际的)
2026年5月26日
研究记录更新
最后更新发布 (实际的)
2026年5月26日
上次提交的符合 QC 标准的更新
2026年5月18日
最后验证
2026年5月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- IRB-20260080-R
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
IPD 计划说明
All data relevant to the study will be generated in the article or uploaded as supplementary information.
Deidentified participant data will be available from Dr. Hui Wang (wang71hui@zju.edu.cn) on a reasonable request.
Protocols and statistical analysis plans will be included as supplementary information.
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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