Carcinoma, Basal Cell
Conditions
Brief summary
A prospective clinical, uncontrolled, open-label, explorative phase 2a trial on patients with histologically-confirmed superficial and nodular basal cell carcinoma (BCC). The study assesses tolerability and tumor clearance after laser-assisted topical delivery of topical ingenol mebutate.
Detailed description
Patients will receive ablative fractional laser (AFXl)-assisted ingenol mebutate (IM) as a treatment for their cutaneous basal cell carcinoma (BCC). Treatment areas consisting of tumors and a 5 mm margin will undergo AFXl exposure (CO2 laser) followed by IM 0.015% or 0.05% under occlusion for 2-3 days. . local skin reactions are monitored at baseline (day1), day 3/4, day 8, day 15, day 29, day 90, and tumor response monitored at baseline, day 29, and day 90. An additional repeat AFXl-IM treatment on day 29 will be offered if tumors persist, based on clinical evaluation and imaging on day 30. Primary outcome: 1. severity and duration of clinical local skin reactions including erythema, scaling, edema, blistering, erosion/ulceration and crusting using a 0-4-point scale at all visits from baseline to day 90. 2. To monitor BCC tumor response on clinical assessments supported by non-invasive imaging techniques including optical coherence tomography (OCT) and reflectance confocal microscopy (RCM) at baseline, day 29 and day 90.
Interventions
DRUGAFXl-assisted ingenol mebutate delivery
Patients will receive ablative fractional laser (AFXl)-assisted ingenol mebutate (IM) as a treatment for their cutaneous basal cell carcinoma (BCC). Treatment areas consisting of tumors and a 5 mm margin will undergo AFXl exposure (CO2 laser) followed by IM 0.015% or 0.05% under occlusion for 2-3 days. . local skin reactions are monitored at baseline (day1), day 3/4, day 8, day 15, day 29, day 90, and tumor response monitored at baseline, day 29, and day 90. An additional repeat AFXl-IM treatment on day 29 will be offered if tumors persist, based on clinical evaluation and imaging on day 30.
Sponsors
LEO Pharma
Merete Haedersdal
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Subjects who meet all of the following criteria are eligible to participate in this study * Patients with histologically verified, low-risk, previously untreated superficial or nodular BCCs on the scalp, face, extremities or trunk * \> 18 years of age at baseline * Legally competent, able to give verbal and written consent * Communicate in Danish verbally as well as in writing * Subject in good general health, is willing to participate and able to give informed consent, and can comply with protocol requirements. * Fitzpatrick skin phototype I-III * Female subjects of childbearing potential must be confirmed not pregnant by a negative urine pregnancy test prior to trial treatment.
Exclusion criteria
Subjects meeting any one of the following criteria are not eligible to participate in this study * Patients with o High-risk BCC * Tumors on the following anatomical locations: * Midface region * Orbital areas * Ears * ii. Size: * \> 20 mm in facial/scalp areas * \> 50 mm in non-facial/non-scalp areas * Subtype: * Morpheaform * Medical history * Gorlin syndrome o Immunosuppressive medication * Subjects with a known allergy to IM. * Individuals with other skin diseases in the area of research interest * Subjects with tattoo in the treatment area which may interfere with or confound evaluation of the study * Subjects with a history of keloids which is deemed clinically relevant in the opinion of the investigator * Subjects with Fitzpatrick skin phototype IV-VI * Lactating or pregnant women
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in occurrence of local skin reactions | 0-90 days | Non-blinded, clinical evaluation of local erythema, edema, flaking, crusting/scabbing, pustulation, scarring, hypo(hyperpigmentation, infection in treated areas will be performed by physician using an FDA-approved 0-4 point lsr scale at day 1, 3/4, 8, 15, 29 and 90 after AFXl exposure. Standardized, clinical photographs are taken to document skin reactions at each visit |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Tumor response clinically | baseline, day 29, day 90 | Tumor clearance (yes or no) will be evaluated clinically at baseline, at day 29 and day 90. If residual tumor is identified at day 90 patients will receive conventional treatment according to national guidelines. |
| Tumor response by imaging techniques | baseline, day 29, day 90 | Clearance (yes or no) will be evaluated using non-invasive reflectance confocal microscopy and optical coherence tomography at baseline, day 30 and day 90.f residual tumor is identified at day 90 patients will receive conventional treatment according to national guidelines. |
| Tumor response - histology | At day 90 | HIstological verification of tumor clearance will be performed at day 90 after first treatment using tissue sections from a punch biopsy (up to 4 mm). If residual tumor is identified at day 90 patients will receive conventional treatment according to national guidelines. |
Countries
Denmark
Outcome results
None listed