Overview
Efficacy of Personalised Irradiation with Rhenium-Skin Cancer Therapy (SCT) for the treatment of non-melanoma skin cancer; a phase IV multi-centre, international, open label, single arm study.
Eligibility
Inclusion Criteria:
- Stage I or II BCC or SCC (SCC Well to Moderately Differentiated), and clinically node negative disease
- Confirmed Histology, and with depth of lesion noted
- Subjects with up to 3 lesions suitable to enter the study (subjects with more than 3 lesions are not excluded from the study, however 3 target lesions are determined for study evaluation only.)
- Subjects able and willing to comply with the requirements of the study
- Age >=18 years
- Informed Consent signed by the subject consenting to undergo the study
- Lesions up to 8cm2
- Lesions with a depth up to 3mm confirmed on biopsy report AND deemed appropriate clinically by treating clinician
- Subjects who are not deemed suitable for surgery, for example due to tumour location, performance status or other comorbidities as deemed relevant by the treating clinician
- Patients who may have declined Surgery and/or fractionated Radiation Therapy
Exclusion Criteria:
- Inability to personally provide written informed consent or to understand and collaborate throughout the study
- Inability or unwillingness to comply with study requirements
- Prior treatment with surgery or radiation therapy for their target lesion(s)
- Depth of lesion greater than 3mm as defined by Biopsy and/or clinical assessment
- Lupus and Scleroderma
- Basal cell naevus syndrome, xeroderma, vitiligo and albinism
- Prior laser at the tumour site
- Malignant melanoma systemic therapy ongoing
- Any ongoing treatment for malignancy, or in the last 4 weeks prior to study entry
- A tumour affecting nerves or bony structures
- Clinical concern of metastatic disease
- Pregnancy and/or Lactation
- Pathological exclusions: Perineural Invasion, Lymphovascular invasion
- Anatomical exclusions: NMSC's of the Medial canthus, eyelid margin (upper and lower), Vermillion lip