The Addition of Pembrolizumab to Postoperative Radiotherapy in Cutaneous Squamous Cell Cancer of the Head and Neck

Inclusion Criteria

• •Histologic diagnosis of cutaneous squamous cell carcinoma of the head and neck that has been resected with no evidence of gross residual disease (margin positivity is acceptable)
• •Patients must have undergone resection of the disease and demonstrate high risk pathologic features including:
• •* T4
• •* Node positive disease
• •* T2/T3N0 disease with any 1 additional feature, including:
• •* Recurrent Disease
• •* Perineural invasion
• •* Lymphovascular space invasion
• •* Poorly differentiated histology
• •* Positive Margins
• •* Satellitosis or in-transit metastases
• •Patients are required to have computerized tomography (CT) neck and chest or positron emission tomography/computerized tomography (PET/CT) and have no documented evidence of distant metastases
• •Patients must not have a history of the following immunosuppressive conditions:bone marrow transplantation and/or organ transplants and/or chronic rheumatic conditions that require active immunosuppressive therapy. Patients with a history of chronic lymphoid or leukemic malignancies which are not under active therapy (no active therapy within the last 3 months) will be eligible. Patients with chronic lymphoid or leukemic malignancies are eligible with or without active disease as long as they have not had treatment within the past three months.
• •Patients may not have had prior therapy with a checkpoint inhibitor (e.g. anti-CTLA-4, anti-PD-1 or anti-PD-L1 therapy)
• •Patients may not have had prior radiotherapy (\>30Gy) to the area requiring treatment that would result in any overlap of tissue in both fields
• •Patients may have received chemotherapy or radiation for a previous, curatively treated malignancy provided at least 2 years have elapsed and there is no current evidence of disease (patients with previous or concurrent additional skin cancers are eligible)
• •Eastern Cooperative Oncology Group (ECOG) Performance Status 0-1
• •Female subject of childbearing potential should have a negative urine or serum pregnancy within 72 hours prior to receiving the first dose of study medication. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
• •Female subjects of childbearing potential should be willing to use 2 methods of birth control or be surgically sterile, or abstain from heterosexual activity for the course of the study through 120 days after the last dose of study medication. Subjects of childbearing potential are those who have not been surgically sterilized or have not been free from menses for \> 1 year.
• •Male subjects should agree to use an adequate method of contraception starting with the first dose of study therapy through 120 days after the last dose of study therapy.
• •Patients must have adequate laboratory values
• •* Absolute neutrophil count ≥ 1,500/mcL
• •* Platelets ≥ 100,000/mcL
• •* Hemoglobin ≥ 9g/dL or ≥5.6mmol/L without transfusion
• •* Serum creatinine ≤ 1.5 times upper limit of normal (ULN) or measured creatinine clearance ≥60mL/min for subject with creatinine levels \>1.5 times institutional ULN
• •* Serum bilirubin ≤ 1.5 times ULN or direct bilirubin ≤ ULN for subjects with total bilirubin levels \> 1.5 ULN
• •* Aspartate aminotransferase (AST (SGOT)) and alanine aminotransferase (ALT (SPGT)) ≤ 2.5 times ULN or ≤ 5 times ULN for subjects with liver metastases
• •* Albumin ≥ 2.5mg/dL