Testing Pembrolizumab Versus Observation in Patients With Merkel Cell Carcinoma After Surgery, STAMP Trial

Inclusion Criteria:

   - Patient must be >= 18 years of age

   - Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status: 0,
   1, or 2 (However, those patients with a performance state of 3 because they are wheel
   chair bound due to congenital or traumatic events more than one year before the
   diagnosis of Merkel cell carcinoma are eligible).

   - Patient must not be pregnant or breast-feeding due to the unknown effects of the study
   drug in this setting. All patients of childbearing potential must have a blood test or
   urine study within 2 weeks prior to randomization to rule out pregnancy. A patient of
   childbearing potential is anyone, regardless of sexual orientation or whether they
   have undergone tubal ligation, who meets the following criteria: 1) has achieved
   menarche at some point, 2) has not undergone a hysterectomy or bilateral oophorectomy;
   or 3) has not been naturally postmenopausal (amenorrhea following cancer therapy does
   not rule out childbearing potential) for at least 24 consecutive months (i.e., has had
   menses at any time in the preceding 24 consecutive months).

   - Patients on Arm A pembrolizumab (MK-3475) must not conceive or father children by
   using accepted and effective method(s) of contraception or by abstaining from sexual
   intercourse from the time of registration, while on study treatment, and continue for
   120 days after the last dose of study treatment. For patients on Arm B only receiving
   radiation therapy, contraception use should be per institutional standard.

   - Patient must have a histological confirmation of diagnosis of Merkel cell carcinoma
   (MCC), pathologic stages (American Joint Committee on Cancer [AJCC] version 8) I-IIIb.

      - Stage I patients with negative sentinel lymph node biopsy are ineligible.
      Patients who have a positive biopsy or for whom no biopsy was done are eligible.

      - Patients with distant metastatic disease (stage IV) are ineligible.

      - The primary tumor must have grossly negative margins. (Microscopically positive
      margins are allowed).

      - Cancers of unknown primary that have regional disease only are eligible.

      - Complete nodal dissection is not required for eligibility.

   - Patients with all macroscopic Merkel cell carcinoma (either identified by physical
   exam or imaging) have been completely resected by surgery within 16 weeks before
   randomization.

   - All patients must have disease-free status documented by a complete physical
   examination and conventional imaging studies within 8 weeks prior to randomization.

   - Patient may not have a history of distant metastatic disease.

      - NOTE: Loco-regional recurrent disease is acceptable, as long as this is not
      metastatic (prior surgery with or without radiation therapy is acceptable).

   - For patients with initial presentation of Merkel cell carcinoma, patient must have no
   previous systemic therapy or radiation therapy prior to surgery for Merkel cell
   carcinoma and cannot have completed adjuvant radiation therapy for Merkel cell
   carcinoma more than 6 weeks prior to randomization. Patients actively undergoing
   radiation therapy or having completed adjuvant radiation therapy within 6 weeks of
   randomization are eligible, as long as resection date is within 16 weeks of
   randomization. Patients with prior radiation at a non-Radiation Oncology Core (IROC)
   provider are eligible for the trial. If the patient has not received radiation, and
   treatment at a Radiation Oncology Core (IROC) provider is not possible, the patient
   can start and complete radiation prior to randomization, with recommendations to
   follow radiation protocol guidelines with submission of treatment records.

   - White blood count >= 2000/uL (within 4 weeks prior to randomization).

   - Absolute neutrophil count (ANC) >= 1000/uL (within 4 weeks prior to randomization).

   - Platelets >= 75 x 10^3/uL (within 4 weeks prior to randomization).

   - Hemoglobin >= 8 g/dL (>= 80 g/L; may be transfused) (within 4 weeks prior to
   randomization).

   - Creatinine =< 2.0 x institutional upper limit of normal (ULN) (within 4 weeks prior to
   randomization).

   - Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =< 2.5 x
   institutional ULN (within 4 weeks prior to randomization).

   - Total bilirubin =< 2.0 x institutional ULN, (except patients with Gilbert's syndrome,
   who must have a total bilirubin less than 3.0 mg/dL) (within 4 weeks prior to
   randomization).

   - Patients who are human immunodeficiency virus (HIV)+ with undetectable HIV viral load
   are eligible provided they meet all other protocol criteria for participation.

   - Patients with hepatitis B virus (HBV) or hepatitis C virus (HCV) infection are
   eligible provided viral loads are undetectable. Patients on suppressive therapy are
   eligible.

   - Patients must not be on active immunosuppression, have a history of life threatening
   virus, have had other (beside non-melanoma skin cancers, or recent indolent cancers
   e.g.: resected low grade prostate cancer) invasive cancer diagnoses in the last two
   years, or have had immunotherapy of any kind within the last 2 years prior to
   randomization.

   - Patients must not have a history of (non-infectious) pneumonitis that required
   steroids or has current pneumonitis.

   - Operative notes from patient's surgical resection must be accessible.