Dynamic Monitoring of ctDNA and HPV DNA in Plasma for the Early Prediction of Recurrence After Cervical Cancer Surgery

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorThe Third Affiliated Hospital of Guangzhou Medical University

About this trial

Assess the sensitivity, specificity, positive predictive value, and negative predictive value of dynamic monitoring of circulating tumor DNA (ctDNA) combined with circulating HPV DNA (cfHPV DNA) for early prediction of recurrence in cervical cancer post-surgery or post-treatment, and compare its advantages and disadvantages with existing diagnostic methods.

Eligibility criteria

Qualifiers

Patients with newly diagnosed HPV-positive cervical malignancy at stages I-IV who have not undergone surgery, radiation therapy, or chemotherapy.

Patients must be older than 18 years of age.

Cervical cancer patients who are eligible for surgery and/or chemoradiotherapy.

Estimated life expectancy of more than three months.

Disqualifiers

Patients who are participating in other clinical trials.

Pregnant or breastfeeding women.

Patients with severe mental illness.

Patients who voluntarily withdraw.

Trial design

Treatments tested in this trial

  • Assess the risk of recurrence and the efficacy of medication

Treatment groups

No treatment groups listed