Velcade, Melphalan, Prednisone And Thalidomide Versus Velcade, Melphalan, Prednisone in Multiple Myeloma Patients
Study Details
Study Description
Brief Summary
The proposed study will evaluate whether the combination of VELCADE, Thalidomide , Melphalan and Prednisone (V-MPT), as induction treatment for newly diagnosed elderly MM patients, improves outcomes compared to the combination VELCADE-MP.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 3 |
Detailed Description
This phase III study represents a prospective randomized open label multicenter trial to evaluate whether the combination of VELCADE, Melphalan, Prednisone and Thalidomide (V-MPT), as induction treatment for newly diagnosed elderly MM patients, improves outcomes compared to the combination VELCADE-MP.
Subjects will be randomized in a 1:1 allocation between:
Arm A: 250 patients: V-MPT treatment Arm B: 250 patients: V-MP treatment Patients excluded from randomization are to be registered in Arm C. Patients randomized in arm A (Thalidomide based) will be further enrolled in the sub-study about the DVT prophylaxis.
Patients will be evaluated at scheduled visits in up to 3 study periods: pre-treatment, treatment and long-term follow-up (LTFU).
- Pre-treatment period:
Screening visits, performed at study entry. After providing written informed consent to participate in the study, patients will be evaluated for study eligibility After registration subjects will be randomized.
- Treatment period:
Subjects in Arm A will receive:
- Induction therapy:
nine 5-week courses of VELCADE/Melphalan/Prednisone/Thalidomide (V-MPT)
- Maintenance therapy:
Thalidomide in combination with VELCADE
Subjects in Arm B will receive:
- Induction therapy:
nine 5-week courses of VELCADE/Melphalan/Prednisone (V-MP)
-
No maintenance therapy is scheduled At the end of induction treatment or at the time of discontinuation of all study drugs, all patients are to attend study center visits on an every 6 to 8-week basis, until development of confirmed Progressive Disease (PD)
-
LTFU period:
After development of confirmed PD all patients are to be followed for survival every 3 months via telephone or office visit.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Arm A: VMPT Induction therapy with nine 5-week courses of VELCADE/Melphalan/Prednisone/Thalidomide (V-MPT) followed by maintenance therapy with Thalidomide and VELCADE |
Drug: Bortezomib, Melphalan, Prednisone, Thalidomide
Induction therapy:
9 courses with weekly VELCADE (4 doses) in combination with oral Melphalan 9 mg/m2,oral Prednisone 60 mg/m2 once daily on Days 1 to 4 of each course and Thalidomide 50 mg/day continuously. The dose of VELCADE is 1.3 mg/m2 administered as a bolus IV injection, on days 1, 8, 15, 22.
Maintenance therapy:
Thalidomide 50 mg/day continuously in combination with VELCADE 1.3 mg or maximum dose tolerated/m2/2 weeks. The maintenance will be initiated at the end of the 9th course and will be stopped after progression. The median expected duration of the maintenance treatment is approximately 2 years.
Other Names:
|
| Active Comparator: VMP Induction therapy with nine 5-week courses of either VELCADE/Melphalan/Prednisone (V-MP). No maintenance is scheduled. |
Drug: Bortezomib, Melphalan, Prednisone
Induction therapy: 9 courses with weekly VELCADE(4 doses) in combination with oral Melphalan 9 mg/m2 and oral Prednisone 60 mg/m2 once daily on Days 1 to 4 of each course. No maintenance therapy is scheduled
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Determine whether the V-MPT combination improves progression free survival (PFS) [Approximately 24 months]
Secondary Outcome Measures
- Determine whether the VMPT combination improves:Response rate, Overall Survival rate, Time and duration of response, Assess the safety, Assess the prognostic factors [Approximately 24 months]
Eligibility Criteria
Criteria
Inclusion Criteria:
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Age > 65 year old and not a candidate for stem cell transplant, or younger who refuses or is not eligible for high-dose therapy
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Symptomatic multiple myeloma or asymptomatic multiple myeloma with related organ or tissue damage
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Presence of measurable disease
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Karnofsky performance status (PS) > 60%
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Able to read and complete the HRQOL instruments
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Agrees to use an acceptable barrier method for contraception for the duration of the study
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Pretreatment clinical laboratory values within 14 days of randomization:
platelet count ≥ 100x109/L
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hemoglobin ≥ 8 g/dL
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absolute neutrophil count (ANC) ≥ 1.0x109/L
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AST ≤ 2.5 times the upper limit of normal
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ALT ≤ 2.5 times the upper limit of normal
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total bilirubin ≤ 1.5 times the upper limit of normal
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serum creatinine ≤ 2.5mg/dL
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corrected serum calcium <14 mg/dL (<3.5 mmol/L)
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Subjects (or their legally acceptable representatives) must have signed an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study.
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Women of child-bearing potential must agree to use 2 methods of contraception: 1 effective (for example hormonal or tubal ligation) and 1 barrier (for example latex condom, diaphragm) for at least 4 weeks before starting the therapy, during the Treatment Period, and for 4 weeks after the last dose;
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Males must agree to use barrier contraception (latex condoms) when engaging in reproductive activity during the Treatment Period and for 4 weeks after the last dose.
Exclusion Criteria:
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Diagnosis of smoldering multiple myeloma or MGUS.
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Diagnosis of Waldenstrom's disease
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Prior or current systemic therapy for multiple myeloma including steroids (with exception of emergency use of a short course [maximum 4 days] of steroids before randomization or prior or current use of biphosphonates)
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Radiation therapy within 30 days before randomization
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Plasmapheresis within 30 days before randomization
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Major surgery within 30 days before randomization (Kyphoplasty is not considered major surgery)
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History of allergic reaction attributable to compounds containing boron or mannitol, or to Thalidomide
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Peripheral neuropathy Grade 2 or higher, as defined by National Cancer Institute Common Toxicity Criteria (NCI CTC) 3.0
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Uncontrolled or severe cardiovascular disease including myocardial infarction within 6 months of enrollment, New York Heart Association (NYHA) Class III or IV heart failure, uncontrolled angina, clinically significant pericardial disease, or cardiac amyloidosis
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Other malignancy within the past 5 years. Exceptions: basal cell or non metastatic squamous cell carcinoma of the skin, cervical carcinoma in situ or FIGO Stage 1 carcinoma of the cervix
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Concurrent medical condition or disease (e.g., active systemic infection, uncontrolled diabetes, pulmonary disease) that is likely to interfere with study procedures or results, or that in the opinion of the investigator would constitute a hazard for participating in this study
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Use of any investigational drugs within 30 days before randomization.
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Pregnant or lactating women. A serum β-hCG pregnancy test must be performed at the Screening visit, for female patients of child-bearing potential. If the test is positive, the patient must be excluded from the study. Confirmation that the patient is not pregnant must be established by a negative serum or urinary pregnancy test with the result obtained 1 day prior to the Baseline visit (or the day of the visit if results are available before drug delivery).
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | A.O.U. S. Giovanni Battista | Torino | Italy | 10126 |
Sponsors and Collaborators
- Fondazione EMN Italy Onlus
Investigators
- Principal Investigator: Mario Boccadoro, MD, Divisione di Ematologia dell'Università di Torino, A.O.U. S. Giovanni Battista, Torino;Italy
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- GIMEMA-MM-03-05
- 2005-004745-33