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