NOAC9 - Circulating Tumor DNA Guided Follow-Up in Anal Cancer
Anal Cancer
About this trial
This is an interventional diagnostic trial for Anal Cancer focused on measuring Anal cancer, Circulating Tumor DNA, Plasma HPV, Follow-up
Eligibility Criteria
Inclusion Criteria:
- Patients with SCCA eligible for definitive (chemo)radiotherapy
- ≥ 18 of years
- Written and oral consent
Exclusion Criteria:
- Conditions that will contraindicate blood samples
- Conditions that will contraindicate a PET-CT scan.
- Potential lack of compliance to standard FU program and study participation.
Sites / Locations
- Department of Oncology Herlev and Gentofte Hospital
- Department of Oncology, Vejle Hospital
- Aarhus University Hospital
- Tampere University Hospital
- Turku University Hospital
- Haukeland University Hospital
- Oslo University Hospital
- University Hospital of North Norway
- St. Olav's University Hospital
- Sahlgrenska University Hospital
- Skåne University Hospital Lund
- Karonlinska University Hospital
- Norrlands University Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
No Intervention
Experimental
No Intervention
ARM A: HPV positive standard of care follow-up
ARM B: HPV positive ctDNA guided imaging in follow-up
ARM O: HPV negative observational arm
The national follow-up program + collection of blood samples for retrospective translational research
The national follow-up program + ctDNA guided additional imaging + collection of blood samples for retrospective translational research
Patients with HPV negative disease will be included in an observational arm (ARM O) ARM O: The national follow-up program + collection of blood samples for retrospective translational research