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Stage I Multiple Myeloma Treatment (IFM-01-04)

Primary Purpose

Multiple Myeloma

Status
Unknown status
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
zometa
Sponsored by
Centre Hospitalier Universitaire de Nice
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Myeloma focused on measuring stage I multiple myeloma

Eligibility Criteria

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

Inclusion Criteria:

  • stage I multiple myeloma without bones injuries

Exclusion Criteria:

  • abnormal kidney function
  • VIH infection
  • Hepatic incapacity
  • pregnancy
  • Associate pathology

Sites / Locations

  • Service de Medecine interne, Hôpital l'ARCHET, CHU de Nice

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

1

2

Arm Description

patients receiving zometa treatment

No treatment, just follow-up

Outcomes

Primary Outcome Measures

Survival without progress

Secondary Outcome Measures

predictive factors of a fast evolution of multiple myeloma
Secondary effects of zolédronate

Full Information

First Posted
August 12, 2008
Last Updated
March 23, 2012
Sponsor
Centre Hospitalier Universitaire de Nice
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1. Study Identification

Unique Protocol Identification Number
NCT00733538
Brief Title
Stage I Multiple Myeloma Treatment
Acronym
IFM-01-04
Official Title
Stage I Multiple Myeloma Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
February 2009
Overall Recruitment Status
Unknown status
Study Start Date
December 2004 (undefined)
Primary Completion Date
November 2009 (Actual)
Study Completion Date
November 2012 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Nice

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Assessment of survival without progression of stage I MM in two groups: arm A: simple survey and arm B: administration of Zoledronate. Describe different progression's type noticed and define the prognosis factors of a fast evolution.
Detailed Description
RATIONAL: Multiple Myeloma in spite of therapy progresses mainly due to stem cell auto transplant, still remain a deadly disease. About 2000 new cases are diagnosed every year in France. The asymptomatic Stage I MM according to Duries and Salmon's staging are usually only watch over and only treated at progression. Zoledronate is a third generation aminobiphosphonate (BP), probably the most powerful among the available compounds which received market clearance authorisation in MM with bone damage. During MM, bone's hyper resorption is premature. Interactions exist between tumor growth and bone lyses. Zoledronate's got a proper antimyeloma's action (induce plasma cells apoptosis). We propose to test the early use of Zoledronate as soon as stage I MM to delay progression. STUDY'S OBJECTIVES: PRINCIPAL: Assessment of survival without progression stage I MM in two groups: A arm: simple survey and B arm: administration of BP. SECONDARY: Describe different progression's type noticed (bone/extra bone) and define the prognosis factor of a fast stage I MM evolution (standard factors, cytogenetic 13 deletion, bone's restructuring strains: crosslaps, bone alkaline phosphatase), list side effects. STUDY'S KIND: Multicenter international randomised trial, open labelled, with individual profit. CONTRIBUTING CENTERS: Intergroupe Francophone du Myélome's centers. INCLUSIONS CRITERIA: Asymptomatic stage I MM without bone's lesion on the standard radiographs. STUDY'S MONITORING: After checking inclusion and non inclusion specifications, the patient will be included in the study and randomized (A arm or B arm) before all treatment. The randomisation will be done by center and stratified according to the diagnostic date witch a year or not. Arm A: simple survey as standard practice. Arm B: a 15 minutes infusion of Zoledronate every month until progression or a maximum of 18 infusions if no progression. The exams are the one usually defined according to good clinical practices guidelines besides cytogenetic, bone's restructuring strain and serum creatin dosage before each infusion in B arm. STATISTICAL PURPOSES: The minimum number of patients required showing a median survival time increase without progression of 26 months in the control arm and 38 months in the BP arm is about 175 patients in each arm for a 48 months inclusion's period, and a monitoring of 24 months after the last inclusion (i.e. a study's length of 6 years).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Myeloma
Keywords
stage I multiple myeloma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
350 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
patients receiving zometa treatment
Arm Title
2
Arm Type
No Intervention
Arm Description
No treatment, just follow-up
Intervention Type
Drug
Intervention Name(s)
zometa
Intervention Description
patients receiving treatment during their follow-up
Primary Outcome Measure Information:
Title
Survival without progress
Time Frame
every month during 6 years
Secondary Outcome Measure Information:
Title
predictive factors of a fast evolution of multiple myeloma
Time Frame
every month during 6 years
Title
Secondary effects of zolédronate
Time Frame
every month during six years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: stage I multiple myeloma without bones injuries Exclusion Criteria: abnormal kidney function VIH infection Hepatic incapacity pregnancy Associate pathology
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Gabriel FUZIBET, PU-PH
Organizational Affiliation
service de médecine interne, CHU de Nice
Official's Role
Principal Investigator
Facility Information:
Facility Name
Service de Medecine interne, Hôpital l'ARCHET, CHU de Nice
City
Nice
ZIP/Postal Code
06202
Country
France

12. IPD Sharing Statement

Learn more about this trial

Stage I Multiple Myeloma Treatment

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