High Risk Myelodysplasia Treated by Azacytidine : Genetic and Epigenetic (MYRAGE) (MYRAGE)
Primary Purpose
High-risk Myelodysplastic Syndromes With Excess Blasts
Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Myelogram
Sponsored by
About this trial
This is an interventional screening trial for High-risk Myelodysplastic Syndromes With Excess Blasts focused on measuring Myelodysplastic syndromes
Eligibility Criteria
Pre-inclusion Criteria:
- patient benefiting from social welfcare
- patient followed at the University Hospital of Nancy
- patient aged 18 years or older
- patient informed on research organization and having signed an informed pre-inclusion consent
- No personal history of myelodysplastic syndrome
- clinical exam adapted to research
- one or more blood cytopenia
Inclusion Criteria:
- patient benefiting from social welfcare
- patient followed at the University Hospital of Nancy
- patient aged 18 years or older
- patient informed on research organization and having signed an informed inclusion consent
- definitive diagnosis of high risk myelodysplastic syndrome with excess blasts
- eligibility to an Azacytidine therapy as first-line treatment
Exclusion Criteria:
- personal history or current other cancer
- immediate acute myeloid leukemia
- personal history of demethylation treatment
- pregnant or breast feeding women
- life-theatening condition
- guardianship
- imprisoned patients
Sites / Locations
- CHRU de Nancy
- BROSEUSRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Patients with High-risk MDS With Excess Blasts
Arm Description
Outcomes
Primary Outcome Measures
Methylation level of the Differentially Methylated Regions (DMR)
Overall response by IWG 2006 response criteria (complete remission / partial remission / non response)
Secondary Outcome Measures
Methylation level of the Differentially Methylated Regions (DMR)
Cytogenetic response by IWG 2006 response criteria (major / minor / no response)
Hematologic improvement by IWG 2006 response criteria (major / minor / no response)
Transfusion independence (yes/no)
General condition improvement (yes/no)
Full Information
NCT ID
NCT03217903
First Posted
July 3, 2017
Last Updated
August 5, 2019
Sponsor
Central Hospital, Nancy, France
Collaborators
Inserm U954 - N-GERE (Nutrition, Genetics and Exposition to Environmental Risk)
1. Study Identification
Unique Protocol Identification Number
NCT03217903
Brief Title
High Risk Myelodysplasia Treated by Azacytidine : Genetic and Epigenetic (MYRAGE)
Acronym
MYRAGE
Official Title
High Risk Myelodysplasia Treated by Azacytidine : Genetic and Epigenetic (MYRAGE)
Study Type
Interventional
2. Study Status
Record Verification Date
August 2019
Overall Recruitment Status
Unknown status
Study Start Date
October 12, 2017 (Actual)
Primary Completion Date
January 1, 2022 (Anticipated)
Study Completion Date
January 1, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Central Hospital, Nancy, France
Collaborators
Inserm U954 - N-GERE (Nutrition, Genetics and Exposition to Environmental Risk)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Myelodysplastic syndromes (MDS) are the most frequent myeloid neoplasms in Western Countries.They mainly affect patients aged 65 years or older. This is a very heterogenous group of diseases, which prognosis is evaluated with International Prognosis Scoring System. High risk MDS present with high frequency of transformation into acute myeloid leukemia. Treatment of high risk MDS often is based on hypomethylating agents, such as 5'-azacytidine (Azacytidine), with a complete response in approximativel 20% of cases..
This treatment is based on 4-week cycles, with daily injection during the first week and rest during the 3 next weeks of the cycle.
Azacytidine efficacy is commonly evaluated with clinical and biological parameters determined by the International Working Group 2006. These parameters are usually evaluated after at least 6 cycles of treatments.
There is a response with Azacytidine treatment in 60% of cases, including 40% of partial responses and 20% of complete responses. In 40% of patients, there is no response, which means that the disases is stable or in progression under therapy.
In this regard, early evaluation of treatment response is an issue. We want to improve our knowledge about early response criteria in Azacytidine-treated high-risk MDS, focusing on SMD with excess blasts, which represent 30 to 40% of total MDS.
Then, the investigator team want to compare DNA methylation profile at diagnosis and after 3 cycles of Azacytidine treatment.
Main objective :
Identify DNA methylation profiles related to response to Azacytidine therapy, after only 3 cycles of treatment, in high risk MDS with excess blasts.
Secondary objective :
Identify at diagnosis DNA methylation profiles that are predicitive of response to Azacytidin, in high risk MDS with excess blasts.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
High-risk Myelodysplastic Syndromes With Excess Blasts
Keywords
Myelodysplastic syndromes
7. Study Design
Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
32 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Patients with High-risk MDS With Excess Blasts
Arm Type
Experimental
Intervention Type
Diagnostic Test
Intervention Name(s)
Myelogram
Intervention Description
Bone marrow aspiration after 3 cycles of Azacytidine treatment
Primary Outcome Measure Information:
Title
Methylation level of the Differentially Methylated Regions (DMR)
Time Frame
3 months (after 3 cycles of treatment)
Title
Overall response by IWG 2006 response criteria (complete remission / partial remission / non response)
Time Frame
At the treatment response assessment (After 6-12 cycles of treatment up to 52 weeks)
Secondary Outcome Measure Information:
Title
Methylation level of the Differentially Methylated Regions (DMR)
Time Frame
At diagnosis
Title
Cytogenetic response by IWG 2006 response criteria (major / minor / no response)
Time Frame
At the treatment response assessment (After 6-12 cycles of treatment up to 52 weeks)
Title
Hematologic improvement by IWG 2006 response criteria (major / minor / no response)
Time Frame
At the treatment response assessment (After 6-12 cycles of treatment up to 52 weeks)
Title
Transfusion independence (yes/no)
Time Frame
At the treatment response assessment (After 6-12 cycles of treatment up to 52 weeks)
Title
General condition improvement (yes/no)
Time Frame
At the treatment response assessment (After 6-12 cycles of treatment up to 52 weeks)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Pre-inclusion Criteria:
patient benefiting from social welfcare
patient followed at the University Hospital of Nancy
patient aged 18 years or older
patient informed on research organization and having signed an informed pre-inclusion consent
No personal history of myelodysplastic syndrome
clinical exam adapted to research
one or more blood cytopenia
Inclusion Criteria:
patient benefiting from social welfcare
patient followed at the University Hospital of Nancy
patient aged 18 years or older
patient informed on research organization and having signed an informed inclusion consent
definitive diagnosis of high risk myelodysplastic syndrome with excess blasts
eligibility to an Azacytidine therapy as first-line treatment
Exclusion Criteria:
personal history or current other cancer
immediate acute myeloid leukemia
personal history of demethylation treatment
pregnant or breast feeding women
life-theatening condition
guardianship
imprisoned patients
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Julien BROSÉUS, MD, PhD
Phone
(+ 33) 3 83 15 49 14
Email
j.broseus@chru-nancy.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Aurore PERROT, MD, PhD
Phone
(+33) 3 83 15 51 66
Email
au.perrot@chru-nancy.fr
Facility Information:
Facility Name
CHRU de Nancy
City
Nancy
ZIP/Postal Code
54035
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Julien BROSEUS, MCU-PH
Facility Name
BROSEUS
City
Vandoeuvre les Nancy
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Julien BROSEUS
12. IPD Sharing Statement
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High Risk Myelodysplasia Treated by Azacytidine : Genetic and Epigenetic (MYRAGE)
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