(Cost)-Effectiveness of Optical Coherence Tomography (OCT) in Basal Cell Carcinoma (BCC) (ROCTI)
Basal Cell Carcinoma, Optical Coherence Tomography
About this trial
This is an interventional diagnostic trial for Basal Cell Carcinoma focused on measuring Basal Cell Carcinoma, Optical Coherence Tomography, Punch biopsy
Eligibility Criteria
Inclusion Criteria:
- Adult patient (>18 years)
- Clinical and dermoscopic suspicion of BCC
- BCC is in the differential diagnosis and a biopsy would normally be obtained to confirm the diagnosis and subtype or exclude other skin lesions.
Exclusion Criteria:
- Patients with BCC in the high-risk zone of the face (ear, nose, eye region)
- Patients with a large BCC referred to our (tertiary care) head and neck tumour working group.
Sites / Locations
- Maastricht UMC+
Arms of the Study
Arm 1
Arm 2
Other
No Intervention
Optical Coherence Tomography arm
Regular care arm
In the intervention arm, OCT imaging is performed which will take about 3 minutes. The decision on the most adequate treatment strategy will be based directly on the OCT diagnosis, but only when there is certainty about the presence of BCC and BCC subtype according to the OCT diagnosis. A 'safety' biopsy will be performed after the OCT scan. In patients where the OCT diagnosis leaves doubt or it is certain that there is no BCC, a biopsy will be taken anyway and the treatment decision will be based on the result of this punch biopsy.
In patients assigned to regular care, the result of punch biopsy will always be used to decide which treatment is most adequate. Therefore, a next consultation will be planned to discuss the outcome of the biopsy and the intended treatment strategy.