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NCT Number: NCT06495554

Danish Vulva Cancer Recurrence Study

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Aarhus University Hospital, Aarhus N, Denmark

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Primary or recurrent biopsy-verified squamous cell carcinoma of the vulva
  • ≥ 18 years of age
  • Able to understand oral and written information in Danish

Exclusion criteria

  • Active treatment for concurrent cancer and/or dissemination of concurrent cancer

Treatment and study plan

Measurement of circulating tumor-DNA

Diagnostic Test

Liquid biopsies will be collected at baseline and prospectively during follow-up to measure circulating tumor-DNA.

Collection of patient-reported outcomes

Other

Patient-reported outcomes will be collected at baseline and prospectively during follow-up.

Algorithmically determined telephone interview with a nurse

Other

Dependent on the patient's responses on the patient-reported outcome measures.

Primary outcomes

  1. Recurrence-free survival

    Time frame: Two years

  2. Overall survival

    Time frame: Two years

Secondary outcomes

  1. Symptomatology preceding a recurrence

    Time frame: Two years

  2. Improved quality-of-life as a result of proactive management of late effects on an individual level

    Time frame: Two years

  3. Improved survival as a result of proactive management of late effects on group level

    Time frame: Two years

  4. ctDNA detection at time of diagnosis in relation to disease stage

    Time frame: Two years

  5. ctDNA detection after end of treatment in relation to residual disease

    Time frame: Two years

  6. ctDNA detection during surveillance in relation to recurrent disease

    Time frame: Two years

Study contacts

Contact information is provided by the study sponsor or research team.

Louise Krog, BSc.med.

CONTACT

[email protected]

20995607 ext. +45

Pernille T. Jensen, Professor

CONTACT

[email protected]

20952061 ext. +45

Sponsors and collaborators

Lead sponsor

University of Aarhus

Other

Collaborators

  • Aarhus University Hospital
  • Danish Cancer Society
  • Danish Comprehensive Cancer Center
  • Rigshospitalet, Denmark

Registry information

Official study title

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

Acronym: DaVulvaRec

Important dates

Study start
2024
Primary completion
2028
Study completion
2030
First posted
Jul 10, 2024
Registry last updated
Apr 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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