Developing a Combined Molecular Screening and Triage Test for Cervical Cancer in Self-samples (COMBISCREEN)

Universiteit Antwerpen

Status: Enrolling

Conditions: HPV-Related Cervical Carcinoma; Human Papilloma Virus; Uterine Cervical Neoplasm; Uterine Cervical Dysplasia

Treatments: Device: Colli-Pee 20mL device with UCM; Device: Evalyn Brush

Study type: Interventional

Funder types: Other

Identifiers

NCT06598176

B3002023000030

Details and patient eligibility

About

The goal of the COMBISCREEN project is to develop a fully molecular cervical screening and triage approach that is applicable on self-samples, which are an easily accessible and non-invasive source of biomarkers. The project allows a one-step screening and triage modality and thereby identifies women with clinically relevant disease that are in need of treatment.

Full description

Currently, there is still 37% of the Flemish population eligible for cervical cancer screening that remains un(der)screened. Self-collected urine and vaginal samples that can be collected from home and are non-invasive provide an attractive alternative for this group. The aim of this study is to collect different samples from patients with a cervical cancer or a scheduled conization in order to identify potential biomarkers for cervical cancer and cervical intraepithelial neoplasia (CIN). These samples include a home-collected first-void urine (Colli-Pee 20mL prefilled with urine conservation medium (UCM)) and vaginal self-sample (Evalyn Brush), as well as a clinician collected cervical smear, blood sample and when appropriate also a tissue sample. A tissue sample will only be collected when the patient is undergoing surgical procedures for their standard therapy. As such, they do not undergo additional invasive procedures as part of the study. The samples are collected prior to starting therapeutic processes (e.g. conization, chemotherapy, radiotherapy, surgery...). The presence of biomarkers (e.g. human papillomavirus (HPV) and DNA methylation) for cervical cancer and cervical intraepithelial neoplasia (CIN) will be determined and compared in each of the sample types. The results of the biomarker assays will also be compared to clinical results from cytology and histology in order to determine the accuracy.

Enrollment: 100 estimated patients

Sex: Female

Ages: 25 to 64 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Female
• 25 until 64 years old
• Diagnosed with cervical cancer (CIN3+, irrespective of stage) OR in need of conization (irrespective of diagnostic or therapeutic purposes)
• Has not started any form of cancer treatment prior to study enrollment
• Written informed consent must be obtained from patient
• Is able to understand the information brochure and what the study is about

Exclusion criteria

• Women that underwent hysterectomy
• Pregnant women or 6 weeks post-partum
• Treatment for cervical (pre)cancer in the last 6 months before participation in the study
• Participating in another interventional clinical study (where e.g., a medical device, drug, or vaccine is evaluated) at the same time of participating in this study. Participation in another observational or low-interventional clinical study at the same time is allowed.
• Unable to give informed consent
• Patient has severe anaemia
• Patient received blood transfusion two weeks before sample collection
• Blood sampling would compromise patients' overall health
• Patients who are positive for Human Immunodeficiency Virus (HIV), Hepatitis B or Hepatitis C.
• Patients who are alcoholic or drug abusers
• Patients with a history or current evidence of any condition or abnormality that might confound the results of the study, or is not in the best interest of the patient to participate, in the opinion of the investigator.

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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100 participants in 1 patient group

Sample collection

Experimental group

Description:

Women will collect one first-void urine sample and one vaginal self-sample at home, one day prior to a scheduled appointment at the hospital. During the hospital visit, an additional clinician collected cervical smear and a blood sample will be collected for the study. In case, the patient also undergoes a surgical intervention for their standard treatment plan, the tissue that is collected there, will also be used and analysed for our study. Cytology and histology results will be used as reference test.

Treatment:

Device: Evalyn Brush

Device: Colli-Pee 20mL device with UCM