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Velcade®-Melphalan Association in Autologous Stem-Cell Transplantation (ASCT)

Primary Purpose

Multiple Myeloma

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Bortezomib
Sponsored by
University Hospital, Toulouse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Myeloma focused on measuring Multiple Myeloma, Autologous Stem Cells Transplantation, High Dose Melphalan, Bortezomib

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

At time of diagnosis

  • De novo multiple myeloma patients under 65 or in first relapse, in whom screening for chromosome 13 deletion and beta2microglobulin assay have been performed.
  • Salmon and Durie Stage: III, II, I with symptomatic bone lesion (radiological)
  • Patient's written informed consent
  • No clinical signs of heart failure or coronary insufficiency with LVEF>50%
  • No hepatic in insufficiency: bilirubin<35μmol/l and SGOT, SGPT, alkaline phosphatase less than 2.5 N
  • No respiratory insufficiency: normal pulmonary function tests and DLCO>50%
  • No pre-existing renal impairment not related to the disease
  • No history of any other malignant disease with the exception of basal cell carcinoma and stage I cervical cancer
  • Negative HIV serology
  • Effective contraception when justified

At the time of transplantation

  • Good performance status (WHO score≤2)
  • Creatinine≤170μmol/l and no ineligibility criteria for intensification
  • Stem cells harvest ≥ 5x10E6 CD34/kg for 2 ASCT
  • Absence of progressive disease before transplantation

Exclusion Criteria:

  • Known refusal of the subject to participate to the study
  • Female subject who is pregnant or breast-feeding
  • History of allergy to any of the study medications, their analogues, or excipients in the various formulations
  • Main liver insufficiency
  • ≥ Grade 3 peripheral neuropathy on clinical examination within 14 days before enrollment

Sites / Locations

  • Service of Blood Deseases - South Hospital
  • Service of Clinical Hematology - Bocage Hospital
  • Service of Clinical Hematology - Cote Basque Hospital
  • Service of Clinical Hematology - Minjoz Hospital
  • Service of Clinical Hematology - Avicenne Hospital
  • Service of Clinical Hematology - A. Morvan Hospital
  • Service of Clinical Hematology - F. Baclesse Center
  • Service of Clinical Hematology - Army Instruction Hospital of Percy
  • Service of Clinical Hematology - UH of Clermont-Ferrand
  • Service of Oncohematology - Louis Pasteur Hospital
  • Service of Hematology - Bocage Hospital
  • Service of Hematology - General Hospital
  • Service of Hematology - A. Michallon Hospital
  • Service of Hematology - Claude Hurriez Hospital
  • Service of Hematology - Léon Bérard Center
  • Service of Hematology - Edouard Herriot Hospital
  • Service of Hematology - Lyon Sud Hospital
  • Service of Hematology - Paoli Calmette Institute
  • Service of Hematology - Notre Dame du Bon Secours Hospital
  • Service of Blood Deseases - UH of Nantes
  • Service of Clinical Hematology - Archet 1 Hospital
  • Service of Oncology - Archet 1 Hospital
  • Service of Hematology - Hotel Dieu
  • Service of Hematology - Cochin Hospital
  • Service of Blood Deseases - Saint Antoine Hospital
  • Service of Hematology - Jean Bernard Hospital
  • Service of Hematology - R.Debré Hospital
  • Service of Hematology - Pontchaillou Hospital
  • Service of Hematology -Henri Becquerel Center
  • Service of Hematology - Hautepierre Hospital
  • Service of Clinical Hematology - Purpan hospital TSA 40031
  • Service of Onco-Hematology - Bretonneau Hospital
  • Service of Hematology - Brabois Hospital
  • Service of Hematology -Gustave Roussy Institute

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

bortézomib

Outcomes

Primary Outcome Measures

Evaluate the Complete Response and Very Good Partial Response (VGPR) rates 3 months after autologous blood stem cell transplantation conditioned by Velcade-Melphalan

Secondary Outcome Measures

Assess the toxicity of this Velcade-Melphalan conditioning regimen (hematological and visceral toxicity-NCI criteria) - To assess the progression-free survival after transplantation - To assess the overall survival after tran

Full Information

First Posted
March 13, 2008
Last Updated
May 10, 2017
Sponsor
University Hospital, Toulouse
Collaborators
Intergroupe Francophone du Myelome
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1. Study Identification

Unique Protocol Identification Number
NCT00642395
Brief Title
Velcade®-Melphalan Association in Autologous Stem-Cell Transplantation (ASCT)
Official Title
Velcade®-Melphalan Association as Conditioning Regimen Before Autologous Stem-cell Transplantation in Multiple Myeloma Patients Under 65 Years
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
July 2007 (undefined)
Primary Completion Date
October 2008 (Actual)
Study Completion Date
July 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Toulouse
Collaborators
Intergroupe Francophone du Myelome

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Intensification with autologous stem cell (ASCT) is currently the most effective treatment for subjects under 65 and the essential goal is to achieve complete response (CR) or very good partial response (VGPR= greater than 90% reduction of monoclonal component). However, only 50% of patients achieve this CR/VGPR even with tandem ASCT early in the course of disease. Optimization of the conditioning regimen could improve this CR/VGPR rate. The combinaison of Velcade and HD Melphalan has never been evaluated. However, at conventional doses, Velcade potentiates the antimyeloma effect of Melphalan without inducing any common toxicity. This study will be conducted in patients under the age of 65 with de novo multiple myeloma or in first relapse, with Salmon and Durie stage of III, II, I with one symptomatic bone lesion (radiological)and no contraindication to intensification. The primary objective will be to increase the CR/VGPR rate 3 months after autologous peripheral blood stem cell transplantation conditioned by Velcade-Melphalan from 40% to 70%. With alpha=5% and bêta=10%, 61 patients will be included. Secondary objectives will be to assess the toxicity of the Velcade-Melphalan conditioning regimen, the progression-free survival and the overall survival after intensification. Response rates will be evaluated according to the response criteria defined by. Analysis will be performed on an intention-to-treat basis. After conventional induction therapy and PBSC collection, patients will be offered this new conditioning regimen. they will be free to refuse this regimen, in which case they will receive standard intensification therapy by Melphalan 200 mg/m² followed by autologous stem cell transplantation. Evaluation will occur at 3 months post intensification.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Myeloma
Keywords
Multiple Myeloma, Autologous Stem Cells Transplantation, High Dose Melphalan, Bortezomib

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
61 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
bortézomib
Intervention Type
Drug
Intervention Name(s)
Bortezomib
Other Intervention Name(s)
Velcade
Intervention Description
bortezomib-Melphalan
Primary Outcome Measure Information:
Title
Evaluate the Complete Response and Very Good Partial Response (VGPR) rates 3 months after autologous blood stem cell transplantation conditioned by Velcade-Melphalan
Time Frame
3 months after autologous stem cell transplantation
Secondary Outcome Measure Information:
Title
Assess the toxicity of this Velcade-Melphalan conditioning regimen (hematological and visceral toxicity-NCI criteria) - To assess the progression-free survival after transplantation - To assess the overall survival after tran
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: At time of diagnosis De novo multiple myeloma patients under 65 or in first relapse, in whom screening for chromosome 13 deletion and beta2microglobulin assay have been performed. Salmon and Durie Stage: III, II, I with symptomatic bone lesion (radiological) Patient's written informed consent No clinical signs of heart failure or coronary insufficiency with LVEF>50% No hepatic in insufficiency: bilirubin<35μmol/l and SGOT, SGPT, alkaline phosphatase less than 2.5 N No respiratory insufficiency: normal pulmonary function tests and DLCO>50% No pre-existing renal impairment not related to the disease No history of any other malignant disease with the exception of basal cell carcinoma and stage I cervical cancer Negative HIV serology Effective contraception when justified At the time of transplantation Good performance status (WHO score≤2) Creatinine≤170μmol/l and no ineligibility criteria for intensification Stem cells harvest ≥ 5x10E6 CD34/kg for 2 ASCT Absence of progressive disease before transplantation Exclusion Criteria: Known refusal of the subject to participate to the study Female subject who is pregnant or breast-feeding History of allergy to any of the study medications, their analogues, or excipients in the various formulations Main liver insufficiency ≥ Grade 3 peripheral neuropathy on clinical examination within 14 days before enrollment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Murielle ROUSSEL, MD
Organizational Affiliation
Purpan Hospital - UH Toulouse
Official's Role
Principal Investigator
Facility Information:
Facility Name
Service of Blood Deseases - South Hospital
City
Amiens
ZIP/Postal Code
80054
Country
France
Facility Name
Service of Clinical Hematology - Bocage Hospital
City
Angers
ZIP/Postal Code
49033
Country
France
Facility Name
Service of Clinical Hematology - Cote Basque Hospital
City
Bayonne
ZIP/Postal Code
64109
Country
France
Facility Name
Service of Clinical Hematology - Minjoz Hospital
City
Besançon
ZIP/Postal Code
25030
Country
France
Facility Name
Service of Clinical Hematology - Avicenne Hospital
City
Bobigny
ZIP/Postal Code
93009
Country
France
Facility Name
Service of Clinical Hematology - A. Morvan Hospital
City
Brest
ZIP/Postal Code
29609
Country
France
Facility Name
Service of Clinical Hematology - F. Baclesse Center
City
Caen
ZIP/Postal Code
14076
Country
France
Facility Name
Service of Clinical Hematology - Army Instruction Hospital of Percy
City
Clamart
ZIP/Postal Code
92141
Country
France
Facility Name
Service of Clinical Hematology - UH of Clermont-Ferrand
City
Clermont-Ferrand
ZIP/Postal Code
63003
Country
France
Facility Name
Service of Oncohematology - Louis Pasteur Hospital
City
Colmar
ZIP/Postal Code
68024
Country
France
Facility Name
Service of Hematology - Bocage Hospital
City
Dijon
ZIP/Postal Code
21034
Country
France
Facility Name
Service of Hematology - General Hospital
City
Dunkerque
ZIP/Postal Code
59385
Country
France
Facility Name
Service of Hematology - A. Michallon Hospital
City
Grenoble
ZIP/Postal Code
38043
Country
France
Facility Name
Service of Hematology - Claude Hurriez Hospital
City
Lille
ZIP/Postal Code
59037
Country
France
Facility Name
Service of Hematology - Léon Bérard Center
City
Lyon
ZIP/Postal Code
69008
Country
France
Facility Name
Service of Hematology - Edouard Herriot Hospital
City
Lyon
ZIP/Postal Code
69437
Country
France
Facility Name
Service of Hematology - Lyon Sud Hospital
City
Lyon
ZIP/Postal Code
69495
Country
France
Facility Name
Service of Hematology - Paoli Calmette Institute
City
Marseille
ZIP/Postal Code
13273
Country
France
Facility Name
Service of Hematology - Notre Dame du Bon Secours Hospital
City
Metz
ZIP/Postal Code
57038
Country
France
Facility Name
Service of Blood Deseases - UH of Nantes
City
Nantes
ZIP/Postal Code
44035
Country
France
Facility Name
Service of Clinical Hematology - Archet 1 Hospital
City
Nice
ZIP/Postal Code
06202
Country
France
Facility Name
Service of Oncology - Archet 1 Hospital
City
Nice
ZIP/Postal Code
06202
Country
France
Facility Name
Service of Hematology - Hotel Dieu
City
Paris
ZIP/Postal Code
75004
Country
France
Facility Name
Service of Hematology - Cochin Hospital
City
Paris
ZIP/Postal Code
75014
Country
France
Facility Name
Service of Blood Deseases - Saint Antoine Hospital
City
Paris
ZIP/Postal Code
75571
Country
France
Facility Name
Service of Hematology - Jean Bernard Hospital
City
Poitiers
ZIP/Postal Code
86021
Country
France
Facility Name
Service of Hematology - R.Debré Hospital
City
Reims
ZIP/Postal Code
51032
Country
France
Facility Name
Service of Hematology - Pontchaillou Hospital
City
Rennes
ZIP/Postal Code
35033
Country
France
Facility Name
Service of Hematology -Henri Becquerel Center
City
Rouen
ZIP/Postal Code
76038
Country
France
Facility Name
Service of Hematology - Hautepierre Hospital
City
Strasbourg
ZIP/Postal Code
67098
Country
France
Facility Name
Service of Clinical Hematology - Purpan hospital TSA 40031
City
Toulouse
ZIP/Postal Code
31059
Country
France
Facility Name
Service of Onco-Hematology - Bretonneau Hospital
City
Tours
ZIP/Postal Code
37044
Country
France
Facility Name
Service of Hematology - Brabois Hospital
City
Vandoeuvre
ZIP/Postal Code
54511
Country
France
Facility Name
Service of Hematology -Gustave Roussy Institute
City
Villejuif
ZIP/Postal Code
94805
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
19884643
Citation
Roussel M, Moreau P, Huynh A, Mary JY, Danho C, Caillot D, Hulin C, Fruchart C, Marit G, Pegourie B, Lenain P, Araujo C, Kolb B, Randriamalala E, Royer B, Stoppa AM, Dib M, Dorvaux V, Garderet L, Mathiot C, Avet-Loiseau H, Harousseau JL, Attal M; Intergroupe Francophone du Myelome (IFM). Bortezomib and high-dose melphalan as conditioning regimen before autologous stem cell transplantation in patients with de novo multiple myeloma: a phase 2 study of the Intergroupe Francophone du Myelome (IFM). Blood. 2010 Jan 7;115(1):32-7. doi: 10.1182/blood-2009-06-229658. Epub 2009 Nov 2.
Results Reference
result

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Velcade®-Melphalan Association in Autologous Stem-Cell Transplantation (ASCT)

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