STAMP: Surgically Treated Adjuvant Merkel cell carcinoma with Pembrolizumab, a Phase III Trial

This phase III trial studies how well pembrolizumab works compared to standard of care
observation in treating patients with stage I-III Merkel cell cancer that has been
completely removed by surgery (resected). Immunotherapy with monoclonal antibodies, such
as pembrolizumab, may help the body's immune system attack the cancer, and may interfere
with the ability of tumor cells to grow and spread.

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) must 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.