Pembrolizumab and Radiation Therapy in Patients With Relapsed or Refractory Multiple Myeloma

Sponsor
Emory University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03267888
Collaborator
Merck Sharp & Dohme Corp. (Industry)
26
Enrollment
1
Location
1
Arm
61.7
Anticipated Duration (Months)
0.4
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This pilot clinical trial studies the side effects of pembrolizumab and radiation therapy in treating patients with stage I-III multiple myeloma that has come back after a period of improvement or that does not respond to treatment. Monoclonal antibodies, such as pembrolizumab, may block cancer growth in different ways by targeting certain cells. Radiation therapy uses high energy x-rays to kill cancer cells and shrink tumors. Giving pembrolizumab and radiation therapy may work better in treating patients with stage I-III multiple myeloma.

Condition or DiseaseIntervention/TreatmentPhase
  • Biological: Pembrolizumab
  • Radiation: Radiation Therapy
Phase 1

Detailed Description

PRIMARY OBJECTIVE:
  1. To evaluate the safety of concurrent single/low dose radiation therapy (radiotherapy) (8 Gy/1fx) in combination with pembrolizumab in relapsed or refractory myeloma patients.
SECONDARY OBJECTIVES:
  1. To characterize late toxicity (Common Terminology Criteria for Adverse Events [CTCAE] > grade 2 toxicity at 6 and 12 months) and the effect of radiation in combination with pembrolizumab on systemic response rates using international myeloma working group (IMWG) uniform response criteria for multiple myeloma at 6 months and 12 months.

  2. To assess changes in positron emission tomography/computed tomography (PET/CT) as a result of combining pembrolizumab and radiotherapy at 6 months and 12 months.

OUTLINE:

Patients undergo radiation therapy on day 1. Patients also receive pembrolizumab intravenously (IV) over 30 minutes on day 2 or 3. Courses with pembrolizumab repeat every 3 weeks for 2 years in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up at 30 days and then every 12 weeks thereafter.

Study Design

Study Type:
Interventional
Actual Enrollment :
26 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Pilot Study of Pembrolizumab and Single-Fraction, Low-Dose, Radiation Therapy in Patients With Relapsed or Refractory Multiple Myeloma
Actual Study Start Date :
May 29, 2018
Anticipated Primary Completion Date :
Jul 20, 2023
Anticipated Study Completion Date :
Jul 20, 2023

Arms and Interventions

ArmIntervention/Treatment
Experimental: Radiation therapy, pembrolizumab

Patients undergo radiation therapy on day 1. Patients also receive pembrolizumab IV over 30 minutes on day 2 or 3. Courses with pembrolizumab repeat every 3 weeks for 2 years in the absence of disease progression or unacceptable toxicity.

Biological: Pembrolizumab
Given 200 mg/kg IV.
Other Names:
  • Keytruda
  • MK-3475
  • Radiation: Radiation Therapy
    Patients will receive radiotherapy (8 Gy/1 fx) to an extra-osseous site and/or any bony site containing myeloma deposit.
    Other Names:
  • Radiotherapy
  • Outcome Measures

    Primary Outcome Measures

    1. Incidence of adverse events [Up to 12 months after study start]

      Greater than grade 2 toxicity will be assessed by Common Terminology Criteria for Adverse Events. Proportion adverse events will be reported.

    Secondary Outcome Measures

    1. Number of patients achieving any response [Up to 12 months after study start]

      According to International Myeloma Working Group (IMWG) criteria.

    2. Overall response based on baseline changes on positron emission to positron emission tomography/computed tomography [Up to 12 months after study start]

      Will be defined using International IMWG criteria.

    3. Overall survival [From first treatment on course 1, day 1 to the earlier of date of death and/or last follow up, assessed up to 12 months]

      Will be estimated using the Kaplan-Meier product-limit method.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • International Staging System (ISS) stage I-III multiple myeloma that has progressive, relapsed, or refractory disease

    • Able to give informed consent

    • Eastern Cooperative Oncology Group (ECOG) 0-1

    • Relapsed and/or refractory myeloma; there is no minimum or maximum number of previous therapies that a patient may have received previously before being put on the current trial

    • ≥ 1 osseous and/or extra-osseous lesion that can be radiated

    • Candidate for pembrolizumab (as determined by physician, and adequate organ function)

    • Candidate for radiotherapy (as determined by treatment physician); these patients can have symptomatic disease and/or asymptomatic disease; a minimum of one site of radiation is required to any osseous and/or any extra-osseous disease; radiation to any bony parts of the head and neck, skull, spine, ribs, and/or extremities are allowed; radiation to any bony part for documented lytic disease is allowed; radiation to any soft tissue plasmacytoma (including osseous and extra-osseous plasmacytoma) is allowed; the only exclusion criteria for radiation, is central nervous system (CNS) metastases

    • Measurable myeloma disease (urine protein > 200 mg in 24 hours [hr] urine collection, serum free light chain ratio > 100 with an abnormal k/l ratio, serum M protein > 0.5 g/dl); 12 of the 24 patients do not have to have measurable disease

    • Negative urine pregnancy test within 2 weeks for female subjects; female subjects 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

    • Abstinence is acceptable, if this is the usual life style and preferred contraception for the patient

    Exclusion Criteria:
    • Previous anti-programmed cell death protein 1 (PD1) or anti-PD-L1

    • Solitary plasmacytoma

    • Smoldering (asymptomatic) multiple myeloma

    • Currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigational device within 4 weeks of the first dose of treatment

    • Has a diagnosis of immunodeficiency

    • Known history of active TB (Bacillus tuberculosis)

    • Hypersensitivity to pembrolizumab or any of its recipients

    • Known additional malignancy that is progressing or requires active treatment (exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the skin)

    • 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)

    • Known history of, or any evidence of active, non-infectious pneumonitis

    • Active infection requiring systemic therapy

    • Is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the pre-screening or screening visit through 120 days after the last dose of trial treatment

    • Has a known history of human immunodeficiency virus (HIV) (HIV 1/2 antibodies)

    • Has known active hepatitis B (e.g., hepatitis B surface antigen [HBsAg] reactive) or hepatitis C (e.g., hepatitis C virus [HCV] ribonucleic acid [RNA] [qualitative] is detected)

    • Has received a live vaccine within 30 days of planned start of study therapy; NOTE: seasonal influenza vaccines for injection are generally inactivated flu vaccines and are allowed; however intranasal influenza vaccines (e.g., Flu-Mist) are live attenuated vaccines, and are not allowed

    • Patients requiring radiation for CNS diseases are excluded (CNS defined as brain soft tissue/intra parenchymal metastases within the gray and white matter of the brain and/or for cerebrospinal fluid [CSF] disseminated disease, including leptomeningeal carcinomatous disease)

    • Has a history of allogeneic stem cell transplantation

    Contacts and Locations

    Locations

    SiteCityStateCountryPostal Code
    1Emory University/Winship Cancer InstituteAtlantaGeorgiaUnited States30322

    Sponsors and Collaborators

    • Emory University
    • Merck Sharp & Dohme Corp.

    Investigators

    • Principal Investigator: Mohammad K. Khan, MD, PhD, Emory University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Mohammad K. Khan, Principal Investigator, Emory University
    ClinicalTrials.gov Identifier:
    NCT03267888
    Other Study ID Numbers:
    • IRB00097324
    • NCI-2017-01485
    • RAD4106-17
    First Posted:
    Aug 30, 2017
    Last Update Posted:
    Mar 4, 2022
    Last Verified:
    Mar 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 4, 2022