Melphalan, Prednisone, and Thalidomide or Lenalidomide in Treating Patients With Newly Diagnosed Multiple Myeloma - NCT00602641-54601(Clinical Trial 200652)
ClinicalConnection.com has recently undergone an update and this page may no longer be up-to-date. Please Search For Clinical Trials to view the most current clinical trials listings.
| City: |
|
La Crosse |
|
State:
|
|
WI |
| Zip Code: |
|
54601 |
| Conditions: |
|
Multiple Myeloma and Plasma Cell Neoplasm |
| Purpose: |
|
RATIONALE: Drugs used in chemotherapy, such as melphalan and prednisone, work in different
ways to stop the growth of cancer cells, either by killing the cells or by stopping them
from dividing. Thalidomide and lenalidomide may stop the growth of multiple myeloma by
blocking blood flow to the cancer. It is not yet known whether melphalan and prednisone are
more effective when given together with thalidomide or lenalidomide in treating multiple
myeloma.
PURPOSE: This randomized phase III trial is studying giving melphalan and prednisone
together with thalidomide to see how well it works compared with giving melphalan and
prednisone together with lenalidomide in treating patients with newly diagnosed multiple
myeloma.
|
| Study summary: |
|
OBJECTIVES:
Primary
- To compare progression-free survival between patients receiving melphalan, prednisone,
and thalidomide versus melphalan, prednisone, and lenalidomide in newly diagnosed
multiple myeloma patients who are not candidates for high-dose therapy.
Secondary
- To compare overall survival between both arms.
- To compare response rates and depth of response in these patients.
- To compare the incidence of toxicities in these patients.
- To validate the TC classification of myeloma as a prognostic tool using gene expression
profiling at diagnosis.
Tertiary
- To compare quality-of-life (QOL) change between arms based on the FACT-Ntx TOI from
baseline to the end of course 24 (maintenance therapy).
- To examine the impact of differential treatment responses on QOL based on the FACT-Ntx
TOI up to course 38.
- To obtain prospective data on myeloma specific QOL attributes.
OUTLINE: This is a multicenter study. Patients are stratified according to ISS stage (I-II
vs III) and age (< 65 vs ≥ 65). Patients are randomized to 1 of 2 treatment arms.
- Arm I:
- Induction therapy: Patients receive oral melphalan and oral prednisone once daily
on days 1-4, and oral thalidomide once daily on days 1-28. Treatment repeats every
28 days for up to 12 courses in the absence of disease progression or unacceptable
toxicity.
- Maintenance therapy: Patients receive oral thalidomide once daily and continue in
the absence of disease progression.
- Arm II:
- Induction therapy: Patients receive oral melphalan and oral prednisone once daily
on days 1-4, and oral lenalidomide on days 1-21. Treatment repeats every 28 days
for up to 12 courses in the absence of disease progression or unacceptable
toxicity.
- Maintenance therapy: Patients receive oral lenalidomide once daily on days 1-21.
Treatment repeats every 28 days in the absence of disease progression.
Quality of life is assessed at baseline and periodically during treatment.
Peripheral blood and bone marrow samples are collected at baseline for gene expression
profiling analysis.
After completion of study treatment, patients will be followed periodically for 10 years. |
| Criteria: |
|
DISEASE CHARACTERISTICS:
- Newly diagnosed multiple myeloma (MM), meeting the following criteria:
- Bone marrow plasmacytosis with ≥ 10% plasma cells or sheets of plasma cells or
biopsy proven plasmacytoma
- Symptomatic disease with evidence of end-organ damage at initial diagnosis that
prompted the initiation of therapy, including ≥ 1 of the following:
- Anemia
- Hypercalcemia
- Bone disease (lytic bone lesions or pathologic fracture)
- Renal dysfunction
- No smoldering MM, defined by all of the following:
- Serum monoclonal protein ≥ 3 g/dL
- Bone marrow plasma cells ≥ 10% or greater
- Absence of anemia, hypercalcemia, lytic bone lesions, or renal dysfunction
- No monoclonal gammopathy of undetermined significance, defined by all of the
following:
- Serum monoclonal protein < 3 g/dL
- Bone marrow plasma cells ≤ 10%
- Absence of anemia, hypercalcemia, lytic bone lesions, or renal dysfunction
- Previously untreated for MM
- Patients 18 to 64 years old must not be a candidate for autologous stem cell
transplantation or have declined transplantation or other alternative treatment
PATIENT CHARACTERISTICS:
- ECOG performance status 0-2
- Hemoglobin > 7 g/dL
- Platelet count > 75,000/mm³
- ANC > 1,000/mm³
- Creatinine < 2.5 mg/dL AND creatinine clearance (measured or calculated) ≥ 60 mL/min
- Direct bilirubin ≤ 1.5 mg/dL
- ALT and AST ≤ 2.5 times upper limit of normal
- No uncontrolled intercurrent illness that would limit compliance with the study
including, but not limited to, any of the following:
- Uncontrolled hypertension
- Symptomatic congestive heart failure
- Unstable angina
- Uncontrolled cardiac arrhythmia
- Uncontrolled psychiatric illness or social situation
- Prior history of Stevens Johnson syndrome
- No peripheral neuropathy ≥ grade 2
- No active uncontrolled infection
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective double-barrier contraception 4 weeks prior to,
during, and 4 weeks after completion of study treatment
- Must be able to take prophylactic aspirin 325mg/day or low-molecular weight heparin
or coumadin
- No second active malignancy requiring treatment within the past 2 years, except for
basal cell or squamous cell carcinoma of the skin or in situ carcinoma of the cervix
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- No prior treatment for myeloma except for either of the following:
- Prednisone or dexamethasone treatment for myeloma for a duration of less than 4
weeks
- Prednisone or dexamethasone in combination with thalidomide or lenalidomide for
a duration of less than 2 weeks total
- Concurrent bisphosphonates or growth factors (i.e., erythropoietin) for MM allowed
- Concurrent localized radiation therapy is allowed for pain control at the physician's
discretion |
|
|
|
| Study is available at: |
|
Gundersen Lutheran Center for Cancer and Blood
La Crosse, WI 54601
United States
Primary Contact:
Clinical Trials Office - Gundersen Lutheran Cancer Center
Email: cancerctr@gundluth.org
Phone: 608-775-2385 |
|
|
If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
|
| Trials Alerts: |
|
If you would like to be
notified of new clinical trials as they become available please
register for a free account.
|
|
| Data Source: |
|
ClinicalTrials.gov |
| Date Processed: |
|
March 22, 2011 |
Modifications to
this listing: |
|
Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
|
|
|
|
|
|
|
|