Purpose

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.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Criteria


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.

Study Design

Phase
Phase 3
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Arm A (pembrolizumab, radiation therapy)
Patients receive pembrolizumab IV over 30 minutes on day 1. Treatment repeats every 21 days for up to 17 cycles in the absence of disease progression or unacceptable toxicity. Patients may also undergo standard of care radiation therapy within 14 days of day 1, cycle 1. Patients undergo PET-CT, CT, or MRI throughout the trial. Patients may also undergo blood sample collection as clinically indicated at the discretion of the treating investigator.
  • Procedure: Biospecimen Collection
    Undergo blood sample collection
    Other names:
    • Biological Sample Collection
    • Biospecimen Collected
    • Specimen Collection
  • Procedure: Computed Tomography
    Undergo PET-CT or CT
    Other names:
    • CAT
    • CAT Scan
    • Computed Axial Tomography
    • Computerized Axial Tomography
    • Computerized axial tomography (procedure)
    • Computerized Tomography
    • Computerized Tomography (CT) scan
    • CT
    • CT Scan
    • tomography
  • Procedure: Magnetic Resonance Imaging
    Undergo MRI
    Other names:
    • Magnetic Resonance
    • Magnetic Resonance Imaging (MRI)
    • Magnetic resonance imaging (procedure)
    • Magnetic Resonance Imaging Scan
    • Medical Imaging, Magnetic Resonance / Nuclear Magnetic Resonance
    • MR
    • MR Imaging
    • MRI
    • MRI Scan
    • MRIs
    • NMR Imaging
    • NMRI
    • Nuclear Magnetic Resonance Imaging
    • sMRI
    • Structural MRI
  • Biological: Pembrolizumab
    Given IV
    Other names:
    • BCD-201
    • Keytruda
    • Lambrolizumab
    • MK-3475
    • Pembrolizumab Biosimilar BCD-201
    • SCH 900475
  • Procedure: Positron Emission Tomography
    Undergo PET-CT
    Other names:
    • Medical Imaging, Positron Emission Tomography
    • PET
    • PET Scan
    • Positron emission tomography (procedure)
    • Positron Emission Tomography Scan
    • Positron-Emission Tomography
    • proton magnetic resonance spectroscopic imaging
    • PT
  • Radiation: Radiation Therapy
    Undergo radiation therapy
    Other names:
    • Cancer Radiotherapy
    • Energy Type
    • ENERGY_TYPE
    • Irradiate
    • Irradiated
    • Irradiation
    • Radiation
    • Radiation Therapy, NOS
    • Radiotherapeutics
    • Radiotherapy
    • RT
    • Therapy, Radiation
Active Comparator
Arm B (standard of care observation, radiation therapy)
Patients receive standard of care observation every 3 months for 1 year, and then every 6 months for 5 years. Patients may also undergo standard of care radiation therapy within 14 days of day 1, cycle 1. Patients undergo PET-CT, CT, or MRI throughout the trial. Patients may also undergo blood sample collection as clinically indicated at the discretion of the treating investigator.
  • Other: Best Practice
    Receive standard of care observation
    Other names:
    • standard of care
    • standard therapy
  • Procedure: Biospecimen Collection
    Undergo blood sample collection
    Other names:
    • Biological Sample Collection
    • Biospecimen Collected
    • Specimen Collection
  • Procedure: Computed Tomography
    Undergo PET-CT or CT
    Other names:
    • CAT
    • CAT Scan
    • Computed Axial Tomography
    • Computerized Axial Tomography
    • Computerized axial tomography (procedure)
    • Computerized Tomography
    • Computerized Tomography (CT) scan
    • CT
    • CT Scan
    • tomography
  • Procedure: Magnetic Resonance Imaging
    Undergo MRI
    Other names:
    • Magnetic Resonance
    • Magnetic Resonance Imaging (MRI)
    • Magnetic resonance imaging (procedure)
    • Magnetic Resonance Imaging Scan
    • Medical Imaging, Magnetic Resonance / Nuclear Magnetic Resonance
    • MR
    • MR Imaging
    • MRI
    • MRI Scan
    • MRIs
    • NMR Imaging
    • NMRI
    • Nuclear Magnetic Resonance Imaging
    • sMRI
    • Structural MRI
  • Procedure: Positron Emission Tomography
    Undergo PET-CT
    Other names:
    • Medical Imaging, Positron Emission Tomography
    • PET
    • PET Scan
    • Positron emission tomography (procedure)
    • Positron Emission Tomography Scan
    • Positron-Emission Tomography
    • proton magnetic resonance spectroscopic imaging
    • PT
  • Radiation: Radiation Therapy
    Undergo radiation therapy
    Other names:
    • Cancer Radiotherapy
    • Energy Type
    • ENERGY_TYPE
    • Irradiate
    • Irradiated
    • Irradiation
    • Radiation
    • Radiation Therapy, NOS
    • Radiotherapeutics
    • Radiotherapy
    • RT
    • Therapy, Radiation

More Details

Status
Suspended
Sponsor
National Cancer Institute (NCI)

Study Contact

Detailed Description

PRIMARY OBJECTIVE: I. To compare recurrence free survival (RFS) and overall survival (OS) as co-primary endpoints across the two arms. SECONDARY OBJECTIVES: I. To evaluate adverse events. II. To evaluate distant metastasis free survival (DMFS). III. To evaluate the impact of radiation on clinical outcomes (OS, RFS, DMFS). OUTLINE: Patients are randomized to 1 of 2 arms. ARM A: Patients receive pembrolizumab intravenously (IV) over 30 minutes on day 1 of each cycle. Treatment repeats every 21 days for up to 17 cycles in the absence of disease progression or unacceptable toxicity. Patients may also undergo standard of care radiation therapy within 14 days of day 1, cycle 1. Patients undergo positron emission tomography (PET)-computed tomography (CT), CT, or magnetic resonance imaging (MRI) throughout the trial. Patients may also undergo blood sample collection as clinically indicated at the discretion of the treating investigator. ARM B: Patients receive standard of care observation every 3 months for 1 year, and then every 6 months for 5 years. Patients may also undergo standard of care radiation therapy within 14 days of day 1, cycle 1. Patients undergo PET-CT, CT, or MRI throughout the trial. Patients may also undergo blood sample collection as clinically indicated at the discretion of the treating investigator. After completion of study treatment, patients are followed up every 3-6 months for 5 years from the date of registration.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.