Phase 2
N=101
Tadalafil and Lenalidomide Maintenance With or Without Activated Marrow Infiltrating Lymphocytes (MILs) in High Risk Myeloma
Multiple Myeloma
Bottom Line
View on ClinicalTrials.gov: NCT01858558 ↗Enrolled (actual)
101
Serious AEs
92.1%
Results posted
Jun 2020
Primary outcome: Primary: Feasibility of MILs as Assessed by the Ability to Harvest, Expand, and Infuse the MILs Product — 71; 46; 1; 4 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- aMIL (Biological); No aMIL (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
- Primary completion
- Jun 2019
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Feasibility of MILs as Assessed by the Ability to Harvest, Expand, and Infuse the MILs Product |
71; 46; 1; 4; 1; 1 | — |
| SECONDARY Toxicity as Determined by Total Number of Grade 3 or Higher Adverse Events |
129; 65 | — |
| SECONDARY Overall Survival (OS) |
55 | — |
| SECONDARY Progression-free Survival (PFS) |
21.82 | — |
Summary
This research is being done to find out if altering the immune system by giving activated marrow infiltrating lymphocytes (MILs) can improve outcomes for multiple myeloma patients who receive a standard autologous stem cell transplant.
Eligibility Criteria
Inclusion Criteria
- Age 18 - 80 years old;
- Patients with active myeloma requiring systemic treatment;
- Newly diagnosed patients. Relapsed myeloma patients that have not previously had a transplant;
- Meeting criteria for high-risk disease;
- Measurable serum and/or urine M-protein from prior to induction therapy documented and available. A positive serum free lite assay is acceptable;
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 - 2 (see Appendix C).
- Meet all institutional requirements for autologous stem cell transplantation;
- The patient must be able to comprehend and have signed the informed consent;
- Patients must have had > than PR after last therapy.
Exclusion Criteria
- Diagnosis of any of the following cancers:
- POEMS syndrome (plasma cell dyscrasia with polyneuropathy, organomegaly, endocrinopathy, monoclonal protein [M-protein] and skin changes);
- Non-secretory myeloma (no measurable protein on Serum Free Lite Assay);
- Plasma cell leukemia;
- Diagnosis of amyloidosis;
- Failed to achieve at least a partial response (PR) to latest therapy;
- Previous hematopoietic stem cell transplantation;Patients can have had prior relapsed disease as long as they have never been previously transplanted;
- Known history of HIV infection;
- Use of corticosteroids (glucocorticoids) within 21 days of bone marrow collection;
- Use of any myeloma-specific therapy within 21 days of bone marrow collection;
- Infection requiring treatment with antibiotics, antifungal, or antiviral agents within seven days of registration;
- Participation in any clinical trial within 28 days of registration on this trial, which involved an investigational drug or device;
- History of malignancy other than multiple myeloma within five years of registration, except adequately treated basal or squamous cell skin cancer;
- Active autoimmune disease (e.g., rheumatoid arthritis, multiple sclerosis, systemic lupus erythematosis) requiring active systemic treatment. Hypothyroidism without evidence of Grave's disease or Hashimoto's thyroiditis is permitted.
- Human T-lymphotropic virus (HTLV) 1 or 2 positive;
- Known hypersensitivity to Prevnar or any of its components;
- Contraindication to phosphodiesterase-5 inhibitors (e.g. currently on nitrates).
Data sourced from ClinicalTrials.gov (NCT01858558). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.