- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07606677
Peripheral Blood CyTOF Immune Model for Cervical Lesion Detection in HPV16/18+ Women
18. mai 2026 oppdatert av: 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.
Studieoversikt
Status
Har ikke rekruttert ennå
Detaljert beskrivelse
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).
Studietype
Observasjonsmessig
Registrering (Antatt)
1465
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Junfen Xu
- Telefonnummer: +86 13567147767
- E-post: xjfzu@zju.edu.cn
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
Prøvetakingsmetode
Ikke-sannsynlighetsprøve
Studiepopulasjon
HPV16/18-positive patients
Beskrivelse
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
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
The diagnostic sensitivity of the CyTOF-based immune model for detecting CIN3+ lesions in HPV16/18-positive women
Tidsramme: 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
Tidsramme: 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
Tidsramme: through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
The diagnostic sensitivity of the CyTOF-based immune model for detecting CIN2+ lesions in HPV16/18-positive women,
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Antatt)
15. mai 2026
Primær fullføring (Antatt)
31. mars 2027
Studiet fullført (Antatt)
31. mars 2028
Datoer for studieregistrering
Først innsendt
6. mai 2026
Først innsendt som oppfylte QC-kriteriene
18. mai 2026
Først lagt ut (Faktiske)
26. mai 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
26. mai 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
18. mai 2026
Sist bekreftet
1. mai 2026
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Urogenitale sykdommer
- Kjønnssykdommer
- Urogenitale neoplasmer
- Neoplasmer etter nettsted
- Neoplasmer
- Kvinnelige urogenitale sykdommer
- Kvinnelige urogenitale sykdommer og graviditetskomplikasjoner
- Livmorsykdommer
- Kjønnssykdommer, kvinner
- Genitale neoplasmer, kvinnelige
- Forstadier til kreft
- Livmor livmorhalssykdommer
- Uterine neoplasmer
- Uterine cervikale neoplasmer
- Livmor livmorhalsdysplasi
Andre studie-ID-numre
- IRB-20260080-R
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
IPD-planbeskrivelse
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.
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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