- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT00948922
Melphalan+Bortezomib as a Conditioning Regimen for Autologous and Allogeneic Stem Cell Transplants in Multiple Myeloma
27. August 2019 aktualisiert von: H. Lee Moffitt Cancer Center and Research Institute
Evaluation of Melphalan+Bortezomib as a Conditioning Regimen for Autologous and Allogeneic Stem Cell Transplants in Multiple Myeloma After Cytoreductive Therapy
The purpose of this study is to evaluate the effectiveness of Bortezomib when added to standard chemotherapy medicine(s) for treatment of Multiple Myeloma.
Studienübersicht
Status
Abgeschlossen
Bedingungen
Detaillierte Beschreibung
The primary objectives of this study are:
- To determine the 2 year-progression free survival in multiple myeloma with an allogeneic transplant using a conditioning regimen of melphalan + fludarabine + Bortezomib in patients < 60 years of age and available HLA-matched donor and compare it with the 2 year-progression-free-survival after an autologous stem cell transplant with melphalan+Bortezomib conditioning in patients < 60 years.
- To determine the 2 year-progression free survival in multiple myeloma with an autologous stem cell transplant using a conditioning regimen of melphalan + Bortezomib. for patients > 60 years of age and patients < 60 years of age who decline allogeneic stem cell transplant.
The secondary objectives of this study are:
- To determine the overall survival in multiple myeloma with autologous or allogeneic stem cell transplants using the above conditioning regimens
- To determine the response rates in multiple myeloma using the above regimens.
- To determine minimal residual disease status using allele specific oligonucleotides (ASO-PCR) by PCR and flow-cytometry for multiple myeloma cells.
- To correlate minimal residual disease status with 2 year progression free survival and overall survival.
- To determine the incidence of acute and chronic graft-versus-host disease (GVHD) in multiple myeloma with allogeneic stem cell transplant using the above conditioning regimen.
- To examine quality of life in patients treated with allogeneic and autologous stem cell transplants using the above conditioning regimen.
Studientyp
Interventionell
Einschreibung (Tatsächlich)
124
Phase
- Phase 2
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
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Florida
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Tampa, Florida, Vereinigte Staaten, 33612
- H. Lee Moffitt Cancer Center
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Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
18 Jahre und älter (Erwachsene, Älterer Erwachsener)
Akzeptiert gesunde Freiwillige
Nein
Studienberechtigte Geschlechter
Alle
Beschreibung
Inclusion Criteria:
Multiple Myeloma Criteria(International Uniform Response Criteria for Multiple Myeloma)
- Patients with responsive disease after any line of induction therapy
- A complete response
- A very good partial response
- A partial response
- Patients greater than or equal to 18 years of age are eligible. There is upper age limit of 60 years for allogeneic transplants.
- Patients must have a histologically confirmed diagnosis.
- All patients should have a life expectancy of at least 12 weeks.
- Patients must have undergone a complete psychosocial evaluation and have been considered capable of compliance.
- Meet the following criteria for allogeneic hematopoietic cell transplant:
- Must have an identified donor match defined as: HLA-A, HLA-B, HLA- C, DRB1 8/8 allele matched sibling, family member, or unrelated donor. [7/8 would go on separate mismatched trials] and be < 60 years of age.
- Calculated hematopoietic cell transplantation-specific comorbidity index (HCT-CI) <3
Exclusion Criteria:
- Patients who do not achieve at least a partial response (PR) by the criteria mentioned above with induction therapy.
- Patient has a platelet count of <30 x 10^9/L within 14 days before enrollment.
- Patient has >/= Grade 2 peripheral neuropathy within 30 days before enrollment.
- Patient has an absolute neutrophil count of <1.0 x 10^9/L within 30 days before enrollment.
- Myocardial infarction within 6 months prior to enrollment or has New York Hospital Association (NYHA) Class III or IV heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute ischemia or active conduction system abnormalities. Prior to study entry, any ECG abnormality at screening has to be documented by the investigator as not medically relevant in order for the subject to be considered eligible. Left ventricular ejection fraction (LVEF) by multiple gated acquisition (MUGA) scan < 40%.
- Patient has hypersensitivity to bortezomib, boron or mannitol.
- Female subject is pregnant or breast-feeding. Confirmation that the subject is not pregnant must be established by a negative serum beta-human chorionic gonadotropin (beta-hCG) pregnancy test result obtained during screening. Pregnancy testing is not required for post-menopausal or surgically sterilized women.
- Patient has received other investigational drugs with 30 days before enrollment
- Serious medical or psychiatric illness likely to interfere with participation in this clinical study.
- Patients with a diffusing capacity of lung for carbon monoxide (DLCO) less than 50% (adjusted) of normal or with symptomatic obstructive or restrictive lung disease are ineligible.
- Patients with a total bilirubin greater than 2.0 mg/dL excluding Gilbert's syndrome and serum glutamate oxaloacetate transaminase (SGOT) or serum glutamate pyruvate transaminase (SGPT) greater than two and a half times normal (unless due to primary malignancy), or a history of severe hepatic dysfunction are ineligible.
- Calculated creatinine clearance </= 30 ml/min within 30 days before enrollment
- Patients with active infections are ineligible.
- Patients who are HIV positive are ineligible.
- Patients with active leptomeningeal involvement are ineligible. Patients with a history of previous cerebrospinal fluid (CSF) tumor involvement without symptoms or signs are eligible provided the CSF is now free of disease on lumbar puncture, and MRI of the brain shows no tumor involvement. Patients with severe symptomatic central nervous system (CNS) disease of any etiology are ineligible.
- Patients with uncontrolled insulin-dependent diabetes mellitus defined as a random glucose level of > 400 in the 30 days prior to initiation of study therapy; or uncompensated major thyroid or adrenal dysfunction are ineligible.
- Patients with an Eastern Cooperative Oncology Group (ECOG) performance status of >/= 2(Karnofsky < 50%) are ineligible.
- Patients with an ECOG performance status of 2 to 3(Karnofsky 30-50%), secondary to bone pain, may be enrolled.
- Patients with an ECOG performance status of 2 to 3(Karnofsky 30-50%), secondary to a potentially reversible disease-related problem, may be enrolled.
- Patients with any previous malignancy other than non-melanoma skin cancer are ineligible, unless the patient is without evidence of disease >/= 5 years after the treatment for the cancer was completed.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Nicht randomisiert
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Sonstiges: A: Allogeneic Stem Cell Transplant
Allogeneic Stem Cell Transplant: Fludarabine+Melphalan+Bortezomib followed by Allogeneic Rescue.
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AUTOLOGOUS ARM: Day -3 bortezomib (1.3 mg/m^2) as an intravenous push over 3 to 5 seconds (follows Melphalan infusion).
ALLOGENEIC ARM: Day -3 bortezomib (1.3 mg/m^2) as an intravenous push over 3 to 5 seconds (follows fludarabine and melphalan infusion).
Andere Namen:
AUTOLOGOUS ARM: Day -4 and Day -3 Melphalan 100 mg/m^2/day IV over 30 minutes.
ALLOGENEIC ARM: Day -4, Day -3 Melphalan 70 mg/m^2/day IV over 30 minutes.
Andere Namen:
Days -6,-5,-4,-3 Fludarabine 30 mg/m^2/day IV
Andere Namen:
Allogeneic Stem Cell Transplant: Allogeneic Peripheral Blood Stem Cell Rescue.
Day 0 Infusion of allogeneic peripheral blood stem cells.
For the allogeneic matched-related donors peripheral blood stem cells will be harvested with GCSF mobilization and infused fresh to the recipients.
Allogeneic donor stem cells may also be cryopreserved if they cannot be infused fresh.
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Sonstiges: B: Autologous Stem Cell Transplant
Autologous Stem Cell Transplant: Melphalan+Bortezomib followed by Autologous Rescue.
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AUTOLOGOUS ARM: Day -3 bortezomib (1.3 mg/m^2) as an intravenous push over 3 to 5 seconds (follows Melphalan infusion).
ALLOGENEIC ARM: Day -3 bortezomib (1.3 mg/m^2) as an intravenous push over 3 to 5 seconds (follows fludarabine and melphalan infusion).
Andere Namen:
AUTOLOGOUS ARM: Day -4 and Day -3 Melphalan 100 mg/m^2/day IV over 30 minutes.
ALLOGENEIC ARM: Day -4, Day -3 Melphalan 70 mg/m^2/day IV over 30 minutes.
Andere Namen:
Autologous Stem Cell Transplant: Autologous Peripheral Blood Stem Cell Rescue.
Stem cell mobilization with granulocyte colony-stimulating factor (GCSF) at a dose of 10 μg/kg/day as per institutional standards.
CD34+ peripheral blood stem cells will be collected following the administration of G-CSF as per institutional standards.
Day 0 Infusion of autologous stem cells.
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Sonstiges: BE: Group B Expansion
Group B Expansion on Bortezomib Maintenance: Autologous Only.
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AUTOLOGOUS ARM: Day -3 bortezomib (1.3 mg/m^2) as an intravenous push over 3 to 5 seconds (follows Melphalan infusion).
ALLOGENEIC ARM: Day -3 bortezomib (1.3 mg/m^2) as an intravenous push over 3 to 5 seconds (follows fludarabine and melphalan infusion).
Andere Namen:
AUTOLOGOUS ARM: Day -4 and Day -3 Melphalan 100 mg/m^2/day IV over 30 minutes.
ALLOGENEIC ARM: Day -4, Day -3 Melphalan 70 mg/m^2/day IV over 30 minutes.
Andere Namen:
Autologous Stem Cell Transplant: Autologous Peripheral Blood Stem Cell Rescue.
Stem cell mobilization with granulocyte colony-stimulating factor (GCSF) at a dose of 10 μg/kg/day as per institutional standards.
CD34+ peripheral blood stem cells will be collected following the administration of G-CSF as per institutional standards.
Day 0 Infusion of autologous stem cells.
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Progression Free Survival (PFS)
Zeitfenster: End of 2 year, post transplant follow-up
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PFS: Number of participants, per treatment arm with progression free survival at time of analysis.
Survival time will be measured from the date of transplant to the date of progression, death or the last follow-up, whichever comes first.
Progressive Disease (PD): Increase of ≥ 25% from lowest response value in any one or more of the following: Serum M-component and/or; Urine M-component and/or; Only in patients without measurable serum and urine M-protein levels; the difference between involved and uninvolved FLC levels.
The absolute increase must be > 10 mg/dL; Bone marrow plasma cell percentage; absolute percentage ≥ 10%; Definite development of new bone lesions or soft tissue plasmacytomas or definite increase in the size of existing bone lesions or soft tissue plasmacytomas; Development of hypercalcemia that can be attributed solely to the plasma cell proliferative disorder.
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End of 2 year, post transplant follow-up
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Overall Survival (OS) Rate
Zeitfenster: End of 2 year, post transplant follow-up
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Overall survival in participants with multiple myeloma treated with Bortezomib (Velcade®) containing conditioning regimen and autologous as well as allogeneic transplantation.
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End of 2 year, post transplant follow-up
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Molecular Complete Response (CR) Rates in Patients With Multiple Myeloma
Zeitfenster: End of 2 year, post transplant follow-up
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Complete Response according to International Myeloma Working Group uniform response criteria.
CR: Negative immunofixation on the serum and urine and disappearance of any soft tissue plasmacytomas and < 5% plasma cells in bone marrow.
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End of 2 year, post transplant follow-up
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Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Percentage of Participants With Acute or Chronic Graft-versus-host Disease (GVHD) Following Transplant
Zeitfenster: End of 2 year, post transplant follow-up
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Percentage of participants with Acute or Chronic GVHD following transplant
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End of 2 year, post transplant follow-up
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Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Mitarbeiter
Ermittler
- Hauptermittler: Melissa Alsina, MD, H. Lee Moffitt Cancer Center and Research Institute
- Hauptermittler: Jose Ochoa-Bayona, MD, H. Lee Moffitt Cancer Center and Research Institute
Publikationen und hilfreiche Links
Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.
Nützliche Links
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Tatsächlich)
18. Juni 2009
Primärer Abschluss (Tatsächlich)
20. April 2017
Studienabschluss (Tatsächlich)
14. Mai 2019
Studienanmeldedaten
Zuerst eingereicht
28. Juli 2009
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
28. Juli 2009
Zuerst gepostet (Schätzen)
29. Juli 2009
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
18. September 2019
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
27. August 2019
Zuletzt verifiziert
1. Juni 2019
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Herz-Kreislauf-Erkrankungen
- Gefäßerkrankungen
- Erkrankungen des Immunsystems
- Neubildungen nach histologischem Typ
- Neubildungen
- Lymphoproliferative Erkrankungen
- Immunproliferative Erkrankungen
- Hämatologische Erkrankungen
- Hämorrhagische Störungen
- Hämostasestörungen
- Paraproteinämien
- Bluteiweißstörungen
- Multiples Myelom
- Neubildungen, Plasmazelle
- Physiologische Wirkungen von Arzneimitteln
- Molekulare Mechanismen der pharmakologischen Wirkung
- Antineoplastische Mittel
- Immunsuppressive Mittel
- Immunologische Faktoren
- Antineoplastische Mittel, alkylierend
- Alkylierungsmittel
- Myeloablative Agonisten
- Melphalan
- Bortezomib
- Fludarabin
Andere Studien-ID-Nummern
- MCC-15697
- XO5271 (Andere Zuschuss-/Finanzierungsnummer: Millennium)
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
Klinische Studien zur Multiples Myelom
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University Hospital, CaenLaphalAbgeschlossen
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PETHEMA FoundationRekrutierungDe novo multiple myeloma | Anitocabtagen -AutoleucelSpanien
Klinische Studien zur Bortezomib
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The First Affiliated Hospital of Soochow UniversityUnbekanntMultiples Myelom durch Labortests nachgewiesenChina
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Zhongnan HospitalRekrutierungAkute myeloische Leukämie | BortezomibChina
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Weill Medical College of Cornell UniversityGlaxoSmithKline; Millennium Pharmaceuticals, Inc.AbgeschlossenNon-Hodgkin-LymphomVereinigte Staaten
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International Extranodal Lymphoma Study Group (IELSG)BeendetLymphom, Schleimhaut-assoziiertes lymphatisches GewebeSchweiz
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Dana-Farber Cancer InstituteBeth Israel Deaconess Medical Center; Brigham and Women's Hospital; Millennium...AbgeschlossenLymphoplasmatisches Lymphom | Waldenströms MakroglobulinämieVereinigte Staaten
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OncotherapeuticsMillennium Pharmaceuticals, Inc.BeendetMultiples MyelomVereinigte Staaten
-
Janssen-Cilag International NVAbgeschlossen
-
University of ArkansasMillennium Pharmaceuticals, Inc.BeendetMultiples MyelomVereinigte Staaten
-
International Extranodal Lymphoma Study Group (IELSG)AbgeschlossenLymphom, Schleimhaut-assoziiertes lymphatisches GewebeSchweiz