Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07493928

HPV After chemoRadioTherapy

Implementation of HPV Testing in Patients After Radiotherapy for Cervical Cancer

Status
Recruiting
Phase
Study type
Observational
Enrollment
120 (estimated)
Sponsor
General University Hospital, Prague · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The HART (HPV After chemoRadiotherapy) study is a prospective multicenter observational trial designed to evaluate the clinical utility of HPV testing in the follow-up of patients treated with definitive chemoradiotherapy (CRT) for cervical cancer. Current surveillance after CRT relies mainly on clinical examination and imaging, while the role of HPV-based molecular monitoring remains insufficiently defined. The study plans to enroll 120 patients with FIGO stage IB-IVA cervical cancer treated with primary radiotherapy with curative intent. HPV detection will be performed using two complementary approaches: PCR-based detection of HPV DNA from a cervical swab and analysis of circulating HPV tumor DNA (ctDNA) in peripheral blood. Samples will be collected before treatment and during follow-up at 3, 12, and 24 months after completion of CRT. The primary objective is to determine the sensitivity of these methods for detecting disease recurrence during a two-year follow-up period. Secondary objectives include evaluation of HPV clearance after treatment, comparison of HPV genotypes before and after therapy in cases of persistence, and comparison of the diagnostic performance of cervical HPV testing and ctDNA detection. The study aims to generate evidence supporting the integration of HPV-based molecular monitoring into routine follow-up, potentially enabling earlier detection of recurrence and more individualized surveillance strategies for patients after CRT for cervical cancer.

Conditions

Timeline

Start date
2026-02-01
Primary completion
2028-02-01
Completion
2030-02-01
First posted
2026-03-25
Last updated
2026-03-25

Locations

1 site across 1 country: Czechia

Source: ClinicalTrials.gov record NCT07493928. Inclusion in this directory is not an endorsement.