- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT00558896
CC-4047 and Dexamethasone in Treating Patients With Relapsed or Refractory Multiple Myeloma or Amyloidosis
A Phase II Trial of CC-4047 Plus Dexamethasone in Patients With Relapsed of Refractory Multiple Myeloma or Amyloidosis
RATIONALE: Biological therapies, such as CC-4047, may stimulate the immune system in different ways and stop cancer cells from growing. Dexamethasone and CC-4047 may stop the growth of cancer cells by blocking blood flow to the cancer. Giving CC-4047 together with dexamethasone may kill more cancer cells.
PURPOSE: This phase II trial is studying how well giving CC-4047 together with dexamethasone works in treating patients with relapsed or refractory multiple myeloma or amyloidosis.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
OBJECTIVES:
- To assess the response rate and duration of remission with low-dose CC-4047 plus dexamethasone in patients with relapsed or refractory multiple myeloma or amyloidosis.
- To assess the toxicity of CC-4047 plus dexamethasone in this patient population.
- To assess in an expansion cohort the response rate with an increase in CC-4047 dose among patients who fail to respond adequately to the initial starting dose following the first 2 courses of treatment.
- To assess the response rate and duration of remission with CC-4047 plus dexamethasone in patients with lenalidomide resistant or refractory multiple myeloma.
- To assess the response rate and duration of remission with CC-4047 plus dexamethasone in patients with previously treated light chain amyloidosis.
- To assess the response rate and duration of remission with low- and high-dose CC-4047 plus dexamethasone in patients with lenalidomide and bortezomib refractory multiple myeloma.
- To assess the response rate and duration of remission with high-dose CC-4047 plus dexamethasone in patients with relapsed or refractory myeloma who received ≤ 3 treatment regimens.
OUTLINE: Patients are grouped according to disease status (relapsed/refractory myeloma [closed to accrual as of 8/5/2008] vs lenalidomide resistant/refractory myeloma [closed to accrual as of 4/2/2009] vs previously treated light chain amyloidosis vs lenalidomide and bortezomib resistant/refractory myeloma {low-dose/day}[closed to accrual as of 11/20/09] vs lenalidomide and bortezomib resistant/refractory myeloma (high-dose/day) vs relapsed/refractory myeloma {high-dose/day}).
Patients receive oral CC-4047 on days 1-28 and oral dexamethasone on days 1, 8, 15, and 22. Treatment repeats every 28 days in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed for 4 weeks and then at 6 months.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Phase 2
Kontakte und Standorte
Studienorte
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Arizona
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Scottsdale, Arizona, Vereinigte Staaten, 85259-5499
- Mayo Clinic in Arizona
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Florida
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Jacksonville, Florida, Vereinigte Staaten, 32224
- Mayo Clinic in Florida
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Minnesota
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Rochester, Minnesota, Vereinigte Staaten, 55905
- Mayo Clinic
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-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
DISEASE CHARACTERISTICS:
- Symptomatic multiple myeloma
Previously treated disease meeting one of the following criteria:
- Have light-chain amyloidosis that has been treated with at least one prior regimen
Symptomatic (relapsed or refractory) multiple myeloma
- Patients must have received 1-3 treatment regimens
- Induction therapy followed by autologous stem cell transplantation and consolidation considered one regimen
Measurable disease, as defined by 1 of the following:
- Serum monoclonal protein ≥ 1.0 g by protein electrophoresis
- More than 200 mg of monoclonal protein in the urine on 24-hour electrophoresis
- Serum immunoglobulin free light chain (FLC) > 10 mg/dL and an abnormal FLC ratio
- Measurable soft tissue plasmacytoma, not previously irradiated
- More than 30% plasma cells in bone marrow
- At least 10% plasma cells as measured by bone marrow aspirate, bone marrow biopsy, or labeling index
- No monoclonal gammopathy of undetermined significance (not applicable for patients with amyloid)
- No smoldering myeloma (not applicable for patients with amyloid)
PATIENT CHARACTERISTICS:
- ECOG performance status 0, 1, or 2
- ANC ≥ 1,000/μL
- Platelet count ≥ 75,000/μL
- Creatinine ≤ 2.5 mg/dL
Not pregnant or nursing
- Women must refrain from breastfeeding during study participation and for at least 28 days after discontinuation of study drug
- Negative pregnancy test
Fertile female patients must use two reliable forms of contraception simultaneously at least 28 days before beginning, during, and at least 28 days after completion of study drug
- The two methods of reliable contraception must include one highly effective method (i.e., intrauterine device [IUD], hormonal [birth control pills, injections, or implants], tubal ligation, or partner's vasectomy) and one additional effective (barrier) method (i.e., latex condom, diaphragm, or cervical cap)
- Fertile male patients must use a latex condom (even if they have undergone a prior vasectomy) while having intercourse with any woman, while taking the drug and for 28 days after stopping treatment
- Men must agree to abstain from donating semen or sperm during study participation and for 28 days after discontinuation of study drug
- Willing to abstain from donating blood during study participation and for 28 days after discontinuation of study drug
- No uncontrolled infection
- No other active malignancy
No New York Heart Association class III or IV cardiac disease (all patients)
- Serum troponin T > 0.10 ng/mL (amyloid patients only)
- No known positivity for HIV or active hepatitis infection
- No active deep vein thrombosis or pulmonary embolism that has not been therapeutically anticoagulated
- No condition, including the presence of laboratory abnormalities, that places the patient at unacceptable risk for participating in the study or confounds the ability to interpret data from the study
- No known hypersensitivity to thalidomide or lenalidomide including development of erythema nodosum if characterized by a desquamating rash
- No peripheral neuropathy > grade 2
PRIOR CONCURRENT THERAPY:
- All previous cancer therapy, including chemotherapy and investigational agents, must have been discontinued ≥ 2 weeks prior to study registration
- No radiotherapy ≤ 14 days prior to study registration
- No other concurrent anti-myeloma therapy
- No concurrent radiotherapy, except for palliation of a single painful bone lesion or fracture
- Routine concurrent bisphosphonate therapy allowed for patients with myeloma bone disease
- Willing and able to take aspirin or alternate prophylactic anticoagulation
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Nicht randomisiert
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Relapsed Myeloma (<4 Prior Regimens)
Pomalidomide: 2 mg orally once daily, days 1-28 of 28 day cycle Dexamethasone: 40 mg on days 1, 8, 15 ad 22 of 28 day cycle |
40 mg/day administered through PO (with food) at Days 1, 8, 15, 22 per cycle.
2 or 4 mg/day administered through PO at days 1 - 28 or days 1-21 (see Arm description for specific dosing).
Andere Namen:
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Experimental: Lenalidomide Refractory Myeloma
Pomalidomide: 2 mg orally once daily, days 1-28 of 28 day cycle Dexamethasone: 40 mg on days 1, 8, 15 ad 22 of 28 day cycle |
40 mg/day administered through PO (with food) at Days 1, 8, 15, 22 per cycle.
2 or 4 mg/day administered through PO at days 1 - 28 or days 1-21 (see Arm description for specific dosing).
Andere Namen:
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|
Experimental: Bortezomib/Lenalidomide Refractory/Relapsed Myeloma
Pomalidomide: 2 mg orally once daily, days 1-28 of 28 day cycle Dexamethasone: 40 mg on days 1, 8, 15 ad 22 of 28 day cycle |
40 mg/day administered through PO (with food) at Days 1, 8, 15, 22 per cycle.
2 or 4 mg/day administered through PO at days 1 - 28 or days 1-21 (see Arm description for specific dosing).
Andere Namen:
|
|
Experimental: Bortezomib/Lenalidomide Relapsed/Refractory Myeloma
Pomalidomide: 4 mg orally once daily, days 1-28 of 28 day cycle Dexamethasone: 40 mg on days 1, 8, 15 ad 22 of 28 day cycle |
40 mg/day administered through PO (with food) at Days 1, 8, 15, 22 per cycle.
2 or 4 mg/day administered through PO at days 1 - 28 or days 1-21 (see Arm description for specific dosing).
Andere Namen:
|
|
Experimental: Relapsed Myeloma (< 4 Prior Regimens)
Pomalidomide: 4 mg orally once daily, days 1-28 of 28 day cycle Dexamethasone: 40 mg on days 1, 8, 15 ad 22 of 28 day cycle |
40 mg/day administered through PO (with food) at Days 1, 8, 15, 22 per cycle.
2 or 4 mg/day administered through PO at days 1 - 28 or days 1-21 (see Arm description for specific dosing).
Andere Namen:
|
|
Experimental: Relapsed/Refractory Myeloma
Pomalidomide: 4 mg orally once daily, days 1-21 of 28 day cycle Dexamethasone: 40 mg on days 1, 8, 15 ad 22 of 28 day cycle |
40 mg/day administered through PO (with food) at Days 1, 8, 15, 22 per cycle.
2 or 4 mg/day administered through PO at days 1 - 28 or days 1-21 (see Arm description for specific dosing).
Andere Namen:
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Experimental: Relapsed Amyloidosis
Pomalidomide: 2 mg orally once daily, days 1-28 of 28 day cycle Dexamethasone: 40 mg on days 1, 8, 15 ad 22 of 28 day cycle |
40 mg/day administered through PO (with food) at Days 1, 8, 15, 22 per cycle.
2 or 4 mg/day administered through PO at days 1 - 28 or days 1-21 (see Arm description for specific dosing).
Andere Namen:
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
The Number of Confirmed Hematologic Responses (Complete, Partial, or Very Good Partial Response)
Zeitfenster: Duration of study (up to 3 years)
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Response that was confirmed on 2 consecutive evaluations
|
Duration of study (up to 3 years)
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Progression Free Survival (PFS)
Zeitfenster: Duration of study (up to 5 years)
|
PFS was defined as the time from registration to progression or death due to any cause. PFS was analyzed using Kaplan Meier method. Progression was defined as any one or more of the following:
|
Duration of study (up to 5 years)
|
|
Duration of Response
Zeitfenster: Duration of study (up to 5 years)
|
Duration of response was calculated from the documentation (date) of first response (CR, VGPR, or PR) until the date of progression or last follow-up in the subset of patients who responded.
Kaplan Meier method was used to compute this outcome.
|
Duration of study (up to 5 years)
|
Mitarbeiter und Ermittler
Sponsor
Mitarbeiter
Ermittler
- Studienstuhl: Martha Q. Lacy, MD, Mayo Clinic
Publikationen und hilfreiche Links
Allgemeine Veröffentlichungen
- Dispenzieri A, Buadi F, Laumann K, LaPlant B, Hayman SR, Kumar SK, Dingli D, Zeldenrust SR, Mikhael JR, Hall R, Rajkumar SV, Reeder C, Fonseca R, Bergsagel PL, Stewart AK, Roy V, Witzig TE, Lust JA, Russell SJ, Gertz MA, Lacy MQ. Activity of pomalidomide in patients with immunoglobulin light-chain amyloidosis. Blood. 2012 Jun 7;119(23):5397-404. doi: 10.1182/blood-2012-02-413161. Epub 2012 Apr 4.
- Lacy MQ, Allred JB, Gertz MA, Hayman SR, Short KD, Buadi F, Dispenzieri A, Kumar S, Greipp PR, Lust JA, Russell SJ, Dingli D, Zeldenrust S, Fonseca R, Bergsagel PL, Roy V, Stewart AK, Laumann K, Mandrekar SJ, Reeder C, Rajkumar SV, Mikhael JR. Pomalidomide plus low-dose dexamethasone in myeloma refractory to both bortezomib and lenalidomide: comparison of 2 dosing strategies in dual-refractory disease. Blood. 2011 Sep 15;118(11):2970-5. doi: 10.1182/blood-2011-04-348896. Epub 2011 Jun 20.
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Herz-Kreislauf-Erkrankungen
- Gefäßerkrankungen
- Stoffwechselerkrankungen
- Erkrankungen des Immunsystems
- Neubildungen nach histologischem Typ
- Neubildungen
- Lymphoproliferative Erkrankungen
- Immunproliferative Erkrankungen
- Hämatologische Erkrankungen
- Hämorrhagische Störungen
- Hämostasestörungen
- Paraproteinämien
- Bluteiweißstörungen
- Proteostase-Mängel
- Multiples Myelom
- Neubildungen, Plasmazelle
- Amyloidose
- Plasmazytom
- Physiologische Wirkungen von Arzneimitteln
- Autonome Agenten
- Agenten des peripheren Nervensystems
- Entzündungshemmende Mittel
- Antineoplastische Mittel
- Immunologische Faktoren
- Antiemetika
- Magen-Darm-Mittel
- Glukokortikoide
- Hormone
- Hormone, Hormonersatzstoffe und Hormonantagonisten
- Antineoplastische Mittel, hormonell
- Angiogenese-Inhibitoren
- Angiogenese-modulierende Mittel
- Wuchsstoffe
- Wachstumshemmer
- Dexamethason
- Pomalidomid
Andere Studien-ID-Nummern
- CDR0000574742
- P30CA015083 (US NIH Stipendium/Vertrag)
- 07-003064 (Andere Kennung: Mayo Clinic IRB)
- NCI-2009-01283 (Registrierungskennung: NCI-CTRP)
- MC0789 (Andere Kennung: Mayo Clinic Cancer Center)
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