Status:
ACTIVE_NOT_RECRUITING
Daratumumab in Treating Transplant-Eligible Patients With Multiple Myeloma
Lead Sponsor:
Mayo Clinic
Conditions:
Plasma Cell Myeloma
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
This phase II trial studies how well daratumumab works in treating transplant-eligible patients with multiple myeloma. Daratumumab is a monoclonal antibody that may interfere with the ability of cance...
Detailed Description
PRIMARY OBJECTIVE: I. To determine the percentage of patients achieving minimal residual disease (MRD) negativity by multiparameter flow cytometry (MPF) after autologous stem cell transplant (SCT) (a...
Eligibility Criteria
Inclusion
- Considered transplant eligible
- Pathologically confirmed diagnosis of multiple myeloma who are transplant eligible and have received any prior induction therapy (with or without maintenance)
- Measurable MRD in bone marrow within 28 days prior to registration (MPF method)
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1, or 2 at registration
- Absolute neutrophil count (ANC) \>= 1,000 cell/mm\^3 without growth factor support, obtained =\< 14 days prior to registration
- Platelets \>= 50,000 cells/mm\^3 for patients who have bone marrow plasmacytosis \< 50% or \>= 30,000 cells/mm\^3 for patients who have bone marrow plasmacytosis of \>= 50%, obtained =\< 14 days prior to registration
- Calculated or measured creatinine clearance \>= 30 ml/min, obtained =\< 14 days prior to registration
- Total bilirubin =\< 1.5 x upper limit of normal (ULN) unless due to Gilbert's syndrome, in which case the direct bilirubin must be =\< 1.5 X ULN, obtained =\< 14 days prior to registration
- Aspartate aminotransferase (AST)/serum glutamic-oxaloacetic transaminase (SGOT) and alanine aminotransferase (ALT)/serum glutamic-pyruvic transaminase (SGPT) =\< 3 x ULN, obtained =\< 14 days prior to registration
- Prothrombin time (PT)/international normalized ratio (INR) =\< 1.5 X ULN, obtained =\< 14 days prior to registration
- Negative urine or serum pregnancy test for women of childbearing potential
- NOTE: females of reproductive potential must adhere to the scheduled pregnancy testing as required in the Revlimid Risk Evaluation and Mitigation Strategy (REMS) program
- Provide informed written consent
- Measurable disease of multiple myeloma at the time specified by one of the following:
- If no relapse prior to transplant, values obtained at the time of diagnosis
- If disease relapse prior to transplant and the patient did not have treatment for the relapsed disease prior to transplant, the values obtained at the time of relapse immediately prior to the transplant.
- If disease relapse prior to transplant and the patient did have treatment for the relapsed disease prior to transplant, the values obtained prior to this therapy, i.e., the time of relapse
Exclusion
- Any previous ASCT for multiple myeloma (MM) (NOTE: Patient may have had prior stem cell collection before registration on the study)
- Any prior therapy with daratumumab
- Non-secretory MM or known amyloid light-chain (AL) amyloidosis
- Clinically significant active infection requiring intravenous antibiotics (=\< 14 days prior to registration)
- \>= grade 3 neuropathy and/or POEMS syndrome (plasma cell dyscrasia with polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes)
- Other prior malignancy
- Exceptions:
- Adequately treated basal cell or squamous cell skin cancer
- Any in situ cancer
- Adequately treated stage I or II cancer from which the patient is currently in complete remission, or
- Any other cancer from which the patient has been disease free for at least 3 years
- Concurrent therapy considered investigational
- NOTE: patients must not be planning to receive any radiation therapy (except localized radiation for palliative care that must be completed prior to starting cycle 1, day 1)
- Pregnant women
- Nursing women (lactating females are eligible provided that they agree not to breast feed while taking lenalidomide)
- Men or women of childbearing potential who are unwilling to employ adequate contraception
- Major surgery =\< 4 weeks prior to registration
- History of stroke/intracranial hemorrhage =\< 6 months prior to registration
- Clinically significant cardiac illness including New York Heart Association (NYHA) class III or class IV heart failure, unstable angina pectoris, myocardial infarction within the past 6 months, or \>= grade 3 cardiac arrhythmias noted =\< 14 days prior to registration
- Known human immunodeficiency virus positive (HIV+) patients
- Known hepatitis B or hepatitis C infection
- Exhibiting clinical signs of meningeal involvement of multiple myeloma
- Known severe chronic obstructive pulmonary disease or asthma defined as forced expiratory volume (FEV1) in 1 second less than \< 60% of expected
Key Trial Info
Start Date :
April 9 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 18 2026
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT03477539
Start Date
April 9 2018
End Date
December 18 2026
Last Update
August 28 2025
Active Locations (1)
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1
Mayo Clinic in Florida
Jacksonville, Florida, United States, 32224-9980