Phase 2
N=36
First Autologous Transplant on Minimal Residual Disease Markers in Previously Untreated Myeloma Undergoing Initial Treatment With Velcade
Multiple Myeloma
Bottom Line
View on ClinicalTrials.gov: NCT01215344 ↗Enrolled (actual)
36
Serious AEs
25.0%
Results posted
Jun 2017
Primary outcome: Primary: The Percent of Patients With Minimal Residual Disease (MRD) Status Changing to Negative at Day 100 (Post-AHCT), Among Patients With MRD Positive at the End of Induction (EOI). — 30 percentage of participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- VELCADE (Drug); Lenalidomide (Drug); Dexamethasone (Drug); DVT prophylaxis (Drug); Bisphosphonates (Drug); Liposomal doxorubicin (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Vanderbilt-Ingram Cancer Center
- Primary completion
- Nov 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY The Percent of Patients With Minimal Residual Disease (MRD) Status Changing to Negative at Day 100 (Post-AHCT), Among Patients With MRD Positive at the End of Induction (EOI). |
30 | — |
| SECONDARY Progression Free Survival by MRD Status at Day 100. |
2.64; NA | — |
Summary
The purpose of this study is to study the MRD status after VELCADE based induction therapy (VELCADE, lenalidomide, dexamethasone or VELCADE, liposomal doxorubicin, dexamethasone) in patients with previously untreated multiple myeloma and study the impact of HDC and ASCT on MRD status post-transplant. Our hypothesis is that MRD-status will continue to increase significantly at 3 months post-transplant and will validate that HDC and ASCT needs to be performed even when patients have achieved major response after induction therapy with novel agents.
Eligibility Criteria
Inclusion Criteria
Confirmed Multiple Myeloma as defined below within 120 days of starting cycle 1:
- Bone marrow plasmacytosis with ≥ 10% plasma cells or sheets of plasma cells or biopsy proven plasmacytoma
- Presence of M protein in serum or urine or both. Conventional M spike, serum free light chains, or 24 hour urine study. Non-secretory myeloma is not eligible for this study.
- In addition patient must have one of the following organ dysfunction criteria
- Hypercalcemia
- Renal insufficiency
- Anemia
- Bone disease manifested by lytic lesion or osteoporosis (if osteoporosis is the only organ dysfunction criteria then BM should have ≥ 30% plasma cells)
- Confirmed Multiple myeloma as defined above within 90 days of starting cycle 1
- The following study assessments must be fulfilled and must be obtained with four weeks of starting cycle 1
- Hemoglobin > 7 g/dL, Platelet count > 75 X 10 to 9th power/L, and Absolute neutrophil count > 1 X 10 to 9th power/L
- Creatinine 30 ml/min/1.72 m2
- Bilirubin ≤ 1.5 mg/dL X ULN
- SGPT (ALT) and SGOT (AST) ≤ 2.5 times the upper limit of normal
- Ejection fraction ≥ 45% as measured by a MUGA scan or 2 D echocardiogram
- Pulmonary function tests show >60% predicted values for FVC, FEV1, and DLCO FEV1 must be > 1 liter.
- No prior systemic therapy with the exception of bisphosphonates for MM
- Prior glucocorticoid therapy for the treatment of multiple myeloma is not permitted EXCEPT if used in conjunction with palliative radiation to prevent vasogenic edema. In that case steroids should have been used for less than 7 days. Prior steroid use for non-malignant disorders is permitted and should have been restricted to less than the equivalent of prednisone 10 mg per day. Prior or concurrent topical or localized steroid therapy to treat non-malignant disorders is permitted
- Prior palliative and/ or localized radiation therapy is permitted provided at least 4 weeks have passed from date of last radiation therapy to starting cycle 1.
- Patients with prior solitary plasmacytoma treated with radiation therapy with curative intent are eligible if the disease has now progressed to active multiple myeloma and meeting all eligibility criteria for the protocol
- ECOG PS 0, 1 or 2
- For women of childbearing potential a negative serum pregnancy test is required within 4 weeks of starting cycle 1 and then every 4 weeks during the first 4 cycles of induction therapy
- Women of child bearing potential must be willing to refrain from sexual intercourse or willing to employ a dual method of contraception, one of which is highly effective (IUD, birth control pills, tubal ligation or partner's vasectomy) and another additional method (condom, diaphragm, or cervical cap) during the entire course of the study (start of therapy until 30 days after stem cell transplant).
- Sexually active males should be willing to use a condom (even if they have had a prior vasectomy) while having intercourse with any women during the course of the study (start of therapy until 30 days after stem cell transplant).
- Voluntary written informed consent before performance of any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the subject at any time without prejudice to future medical care.
Exclusion Criteria
- Patients with smoldering myeloma or monoclonal gammopathy of unknown significance are not eligible
- Age > 70 years or 1.5 × ULN Total Bilirubin
- Grade 2 or higher peripheral neuropathy due to ANY cause
- High index of suspicion of primary amyloid light chain (AL) amyloidosis.
- Patients with uncontrolled inter-current illness including uncontrolled hypertension, symptomatic congestive heart failure, unstable angina, uncontrolled cardiac arrhythmia, uncontrolled psychiatric illness or social situation that would limit compliance or a prior history of Steven Johnson syndrome
- Patients must not have a history of current or previous deep vein thrombosis or
Data sourced from ClinicalTrials.gov (NCT01215344). 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.