Pembrolizumab for the Treatment of PD-1 Naive Cutaneous Squamous Cell Carcinoma

Inclusion Criteria

• Male/female participants who are at least 18 years of age on the day of signing informed consent with histologically confirmed diagnosis of high-risk localized or locooregional cSCC as defined below may be enrolled in this study. * NOTE: Patients are eligible for this trial either at initial presentation for cSCC with locally advanced and/or concurrent regional nodal metastasis; or at the time of recurrence with locally advanced and/or concurrent regional nodal metastasis assuming following criteria are met per the cSCC-specific American Joint Committee on Cancer (AJCC) International Union Against Cancer (UICC) 8th edition staging classification ** T2 and Nx and M0 (tumor > 2 cm and =< 4 cm in greatest dimension) OR; ** T3 and Nx and M0 (tumor > 4 cm or minor bone erosion or perineural invasion or deep invasion) OR; *** Deep invasion is defined as invasion beyond the subcutaneous fat or > 6 mm (as measured from the granular layer of adjacent normal epidermis to the base of the tumor). *** Perineural invasion is defined as tumor cells within the nerve sheath of a nerve lying deeper than the dermis or measuring 0.1 mm or larger in caliber, or presenting with clinical or radiographic involvement of named nerves without skull base invasion or transgression. ** T4 and Nx and M0 (tumor with gross cortical bone/marrow, skull base invasion and/or skull base foramen invasion if deemed surgically resectable) OR; ** Tx and N1-3 and M0 (if deemed surgically resectable) OR; * NOTE: ** If T2, tumors must possess >= 2 National Comprehensive Cancer Network (NCCN)/Brigham and Women's Hospital (BWH) clinical or pathologic risk factor(s) as stated below. ** NCCN/BWH clinical risk factors: *** Tumors >= 20 mm on trunk or extremities (excluding pretibia, hands, feet, nail units, and ankles). *** Tumors >= 10 mm on cheeks, forehead, scalp, neck, or pretibial areas. ** NCCN/BWH pathologic risk factors: *** Poorly defined borders. *** Recurrent tumors. *** Neurologic symptoms to suggest perineural invasion. *** High-risk histologic subtypes including: poorly differentiated tumor, acantholytic (adenoid), adenosquamous, desmoplastic, or metaplastic (carcinosarcomatous) subtypes (as stated in the pathology report or written documentation by Mohs surgeon). *** Histopathologically documented perineural, lymphatic, or vascular involvement (as stated in the pathology report or written documentation by Mohs surgeon) * NOTE: Tumors of any size on the “mask areas” of the face [central face, eyelids, eyebrows, periorbital nose, lips (cutaneous and vermilion), chin, mandible, preauricular and postauricular skin/sulci, temple, ear, genitalia, hands, and feet] are not eligible. * NOTE: Patients with tumors that arise in the setting of chronic inflammation (Marjolin’s ulcer) such as chronic wounds and/or scars are excluded. * NOTE: Determination of surgical resectability must be made before enrollment by the treating surgical oncologist (or otolaryngology [ENT] surgeon or equivalent)
• A male participant must agree to use a contraception of this protocol during the treatment period and for at least 120 days after the last dose of study treatment and refrain from donating sperm during this period
• A female participant is eligible to participate if she is not pregnant, not breastfeeding, and at least one of the following conditions applies: * Not a woman of childbearing potential (WOCBP) OR * A WOCBP who agrees to follow the contraceptive guidance during the treatment period and for at least 120 days after the last dose of study treatment
• The participant (or legally acceptable representative if applicable) provides written informed consent for the trial
• Have at least a single site of measurable disease based on Response Evaluation Criteria in Solid Tumors (RECIST) 1.1. Lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions
• Willing to undergo pre-treatment biopsies. * Prior archival tumor tissue sample are not permitted. * Minimum tissue requirements: core (16G or 18G, 6 cores; preferred), punch or excisional biopsy of a tumor lesion that has not been previously irradiated
• Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1. * ECOG evaluation should be performed at screening and repeated on cycle 1 day 1
• Absolute neutrophil count (ANC) >= 1500/uL (specimen must be collected within 10 days prior to the start of study treatment)
• Platelets >= 100 000/uL (specimen must be collected within 10 days prior to the start of study treatment)
• Hemoglobin >= 9.0 g/dL or >= 5.6 mmol/L (specimen must be collected within 10 days prior to the start of study treatment) * Criteria must be met without erythropoietin dependency and without packed red blood cell (pRBC) transfusion within last 2 weeks
• Creatinine =< 1.5 x upper limit of normal (ULN) OR measured or calculated creatinine clearance (glomerular filtration rate [GFR] can also be used in place of creatinine or creatinine clearance [CrCl]) >= 30 mL/min for participant with creatinine levels > 1.5 x institutional ULN (specimen must be collected within 10 days prior to the start of study treatment) * Creatinine clearance (CrCl) should be calculated per institutional standard
• Total bilirubin =< 1.5 x ULN OR direct bilirubin =< ULN for participants with total bilirubin levels > 1.5 x ULN (specimen must be collected within 10 days prior to the start of study treatment)
• Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamic pyruvic transaminase [SGPT]) =< 2.5 x ULN (=< 5 x ULN for participants with liver metastases) (specimen must be collected within 10 days prior to the start of study treatment)
• International normalized ratio (INR) OR prothrombin time (PT) activated partial thromboplastin time (aPTT) =< 1.5 x ULN unless participant is receiving anticoagulant therapy as long as PT or aPTT is within therapeutic range of intended use of anticoagulants (specimen must be collected within 10 days prior to the start of study treatment)

Exclusion Criteria

• Diagnosis of immunodeficiency, immunosuppression and/or is receiving systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to the first dose of trial treatment
• Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (eg, CTLA-4, OX-40, CD137)
• Prior chemotherapy, targeted small molecule therapy within 2 weeks prior to study day 1 or who has not recovered (i.e., =< grade 1 or at baseline) from adverse events due to a previously administered agent
• Has received prior radiotherapy within 2 weeks of start of study intervention. Participants must have recovered from all radiation-related toxicities, not require corticosteroids, and not have had radiation pneumonitis. A 2-week washout is permitted for palliative radiation (=< 2 weeks of radiotherapy) to non-central nervous system (CNS) disease
• Is currently participating in or has participated in a study of an investigational agent or has used an investigational device within 4 weeks prior to the first dose of study intervention
• A WOCBP who has a positive urine pregnancy test at screening. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required
• Has received a live vaccine within 30 days prior to the first dose of study drug. * Examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus Calmette–Guerin (BCG), and typhoid vaccine. * Seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed; however, intranasal influenza vaccines (eg, FluMist) are live attenuated vaccines and are not allowed
• Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy (in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of immunosuppressive therapy within 14 days prior to the first dose of study drug
• Has active autoimmune disease that has required systemic treatment in the past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs). * Note: Replacement therapy (eg., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment and is allowed
• Concurrent non-hematologic malignancy other than cSCC within 3 years of data of first planned dose of therapy except for tumors with a negligible risk of metastasis and/or death as defined below: * Adequately treated non-invasive malignancies including but not limited to melanoma in situ (MIS), basal cell carcinoma (BCC), carcinoma in situ (CIS) of cervix, or ductal carcinoma in situ (DCIS) of breast may be enrolled. * Low-risk early stage prostate adenocarcinoma (T1-T2a N0 M0 and Gleason score =< 6 and prostate specific antigen [PSA] =< 10 ng/mL) for which the management plan is active surveillance, or prostate adenocarcinoma with biochemical-only recurrence with documented PSA doubling time of > 12 months for which the management plan is active surveillance may be enrolled. * Indolent hematologic malignancies for which the management plan is active surveillance including but not limited to chronic lymphocytic leukemia (CLL)/indolent lymphoma may be enrolled ** Patients with high-risk hematologic malignancies (chronic myelogenous leukemia [CML], acute lymphoblastic leukemia [ALL], AML, Hodgkin’s or non-Hodgkin’s lymphoma) are excluded even if the management plan is active surveillance
• Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis. * Note: Participants with previously treated brain metastases may participate provided they are radiologically stable, i.e. without evidence of progression for at least 4 weeks by repeat imaging (note that the repeat imaging should be performed during screening), clinically stable and without requirement of steroid treatment for at least 14 days prior to first dose of study intervention
• Has severe hypersensitivity (>= grade 3) to pembrolizumab and/or any of its excipients
• Has a history of (non-infectious) pneumonitis that required steroids or has current pneumonitis
• Has an active infection requiring systemic therapy
• Has a known history of human immunodeficiency virus (HIV) infection
• Has a known history of hepatitis B (defined as hepatitis B surface antigen [HBsAg] reactive) and/or known active hepatitis C virus (defined as anti-HCV reactive) infection. * Patients with treated hepatitis B/C with no evidence of active infection may be enrolled
• Has a known history of active TB (Bacillus tuberculosis)
• Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the study, interfere with the subject’s participation for the full duration of the study, or is not in the best interest of the subject to participate, in the opinion of the treating investigator
• Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial
• Is pregnant or breastfeeding or expecting to conceive or father children within the projected duration of the study, starting with the Screening visit through 120 days after the last dose of trial treatment
• Has had an allogenic tissue/solid organ transplant