Sentinel Lymph Node Biopsy for Cutaneous Squamous Cell Carcinoma of the Head and Neck
Cutaneous Squamous Cell Carcinoma, Sentinel Lymph Node
About this trial
This is an interventional treatment trial for Cutaneous Squamous Cell Carcinoma
Eligibility Criteria
Inclusion Criteria: high risk features rendering the patient eligible for SLNB in this study will include two or more of the following clinical or pathological features:
- Immunocompromised
- Size more than 2 cm
- Depth more than 6 mm
- Poorly differentiated histology
- Perineural invasion > 0.1mm
- Extensive lymphovascular invasion
Exclusion Criteria:
- Evidence of lymph node metastasis (clinical, radiological, or pathological)
- Previous surgery altering lymphatic drainage of the head and neck, such as a prior neck dissection or prior neck irradiation
- Pregnancy of breast-feeding
Sites / Locations
- Jewish General HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Sentinel Lymph Node Biopsy
Standard of Care
Lymphoscintigraphy will be ordered alongside usual pre-operative investigations. Intra-operatively, the excision of the primary tumor will be done with the aim of histologically clear margins and appropriate closure as per routine practice at the operating surgeon's discretion. The patients are injected with technicium 99 pre-operatively and a sentinel lymph node biopsy will be performed with a handheld gamma probe.
These patients will be treated with standard of care, which is wide local excision of the primary tumor without performance of sentinel lymph node biopsy, if not indicated.