Skip to content

Dynamic Study of Circulating Free DNA in Peripheral Blood of Advanced and Recurrent Metastatic Cervical Cancer

Dynamic Study of Circulating Free DNA in Peripheral Blood of Advanced and Recurrent Metastatic Cervical Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116570
Enrollment
Unknown
Registered
2026-01-12
Start date
2026-01-15
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced and recurrent metastatic cervical cancer.

Interventions

Advanced stage (stage II-IVA) :N/A
Late stage (stage IVB and recurrent metastatic) :N/A

Sponsors

Zhejiang Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Cervical cancer (any histological type) confirmed by pathological diagnosis; 2.Including patients with clinical staging of stage II-IVA, stage IVB, and recurrent metastatic cervical cancer; 3.PCR testing of cervical exfoliated cells or serum confirmed positive for high-risk HPV genotypes; 4.Patients receive anti-tumor treatment according to clinical guidelines; 5.Blood samples are collected before, during, after treatment, and during follow-up, with 0.5 ml of plasma/serum per sample; 6.Blood samples are from clinically remaining samples and stored in a biobank; 7.KPS score >= 70; 8.Age 18-80; 9.ECOG performance status score 0-2; 10.patients with follow-up conditions.

Exclusion criteria

Exclusion criteria: 1.Cervical cancer patients with no pathological support for the primary lesion; 2.Those in whom double primary or multiple primary cancers cannot be excluded; 3.Patients with a history of or current other malignant tumors; 4.low-risk HPV infection; 5.PCR testing for HPV typing in cervical cancer tissue, cervical exfoliated cells, and serum all show HPV negative; 6.Patients whom the investigator deems unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Serum/Plasma HPV Cell-Free DNA (cfDNA);

Countries

China

Contacts

Public ContactZhuomin Yin

Zhejiang Cancer Hospital

yinzm@zjcc.org.cn+86 571 8812 2032

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026