The Value of Patient-reported Outcome Measure Assessment and Circulating Tumor-DNA to Detect Early Relapse During Surveillance in Women With Vulva Cancer

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Diagnostic test, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The overall aim is to investigate different aspects of recurrence detection in women with vulva cancer (VC) to identify optimal treatment- and surveillance programs. DaVulvaRec is a Danish nationwide multicenter study with patient inclusion from Aarhus University Hospital and Rigshospitalet, Denmark. Applying a mixed method research design, the investigators will collect and analyze patient-reported outcome measures in combination with procedural data to evaluate symptomatology and map actions taken during the patient's pathway from primary disease to recurrence. Furthermore, the investigators aim to examine if circulating tumor-DNA (ctDNA) can be detected in liquid biopsies from VC patients. All patients will be followed for two years or until recurrence. Patient-reported outcome measures will be completed every four months during surveillance, and liquid biopsies will be collected prospectively for later analyses. Total number of patients to be included is 295 according to a power calculation. All patients in the clinical study will be included in the intervention group, while data on a historical control group will be obtained from The Danish Gynecological Cancer Database. Hence, the control group will consist of 1000 VC patients diagnosed between 2011-2022. Hypotheses: * All patients with VC will have specific tumor markers in the primary tumor that will be detectable in liquid biopsies as ctDNA at the time of diagnosis. * Measurement of ctDNA after primary treatment and during surveillance will allow detection of residual disease, improve allocation for adjuvant treatment, and will allow early detection of recurrent VC. * Proactive use of repeated PROM assessments in combination with procedural actions during surveillance will allow early detection of recurrent VC and early identification of late effects after treatment.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Primary or recurrent biopsy-verified squamous cell carcinoma of the vulva

• ≥ 18 years of age

• Able to understand oral and written information in Danish

Locations
Other Locations
Denmark
Aarhus University Hospital
RECRUITING
Aarhus N
Copenhagen University Hospital
RECRUITING
Copenhagen
Contact Information
Primary
Louise Krog, BSc.med.
loukrg@rm.dk
20995607
Backup
Pernille T. Jensen, Professor
petije@rm.dk
20952061
Time Frame
Start Date: 2024-08-15
Estimated Completion Date: 2030-12-31
Participants
Target number of participants: 1295
Treatments
Experimental: PROM assessment and ctDNA detection during surveillance
All participants (n=295) included in the prospective clinical study
No_intervention: Standard surveillance
Historical controls (n=1,000) who will be identified by the Danish Gynecological Cancer Database
Related Therapeutic Areas
Sponsors
Leads: University of Aarhus
Collaborators: Danish Comprehensive Cancer Center, Danish Cancer Society, Aarhus University Hospital, Rigshospitalet, Denmark

This content was sourced from clinicaltrials.gov