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Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Myelodysplastic Syndrome Low Risk

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT02757989
Recruitment Status : Recruiting
First Posted : May 2, 2016
Last Update Posted : May 27, 2019
Neovii Biotech
Information provided by (Responsible Party):
Groupe Francophone des Myelodysplasies

Brief Summary:
Comparison of survival in patients with or without a matched donor at 36 months

Condition or disease Intervention/treatment Phase
MDS Other: transplantation Not Applicable

Detailed Description:

Patients with a matched donor (8/8 at molecular level unrelated donor or matched sibling) received an allogeneic hematopoietic stem cell transplantation.

Patients without a matched donor received the best available treatment. All patients will be followed at least 36 months or until the end of the study.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 105 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Low or Intermediate-1 Myelodysplastic Syndrome: A Prospective Multicenter Phase II Study Based on Donor Availability on Behalf of the GFM & SFGM-TC
Actual Study Start Date : May 31, 2016
Estimated Primary Completion Date : May 2020
Estimated Study Completion Date : April 2021

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Experimental: Patients with donor
Patients with a matched donor (8/8 at molecular level unrelated donor or matched sibling)
Other: transplantation
allogeneic hematopoietic stem cell transplantation in patients with donor

No Intervention: Patients without donor
Patients without a matched donor

Primary Outcome Measures :
  1. overall survival [ Time Frame: 36 months ]
    comparison of overall survival in patients with or without a matched donor (8/8 unrelated donor or matched sibling) at 36 months

Secondary Outcome Measures :
  1. quality of life [ Time Frame: 12, 24 and 36 months ]
    comparison of quality of life in patients with or without a matched donor, quality of life assessed by questionnaire (EORTC version 3) at inclusion, 12, 24 and 36 months

  2. number of patients with complete response at 36 month [ Time Frame: 36 months ]
    comparison between patients with or without a donor for cumulative incidence of complete response at 36 month

  3. number of patients with transformation in AML at 36 month [ Time Frame: 36 months ]
    comparison between patients with or without a donor for cumulative incidence of transformation in AML at 36 month

  4. proportion of patients with iron overload [ Time Frame: 16 months ]
    proportion of patients with iron overload (Serum Ferritin (SF)>1000 ng/mL or Red Blood Cells transfusion>20) at time of inclusion and at 16 month after inclusion for non-transplanted patients and 12 months post-transplant for transplanted patients

  5. evolution of innovative iron markers including Non-transferrin binding iron (NTBI), labile plasmatic Iron (LPI) and Hepcidine [ Time Frame: 3 and 16 months ]
    evolution of innovative iron markers including Non-transferrin binding iron (NTBI), labile plasmatic Iron (LPI) and Hepcidine measured at time of inclusion, at 3 month and 16 month post-inclusion for all patients; In transplanted patients these markers will be measured just before conditioning regimen (J-5), Just before the transplantation (J0), at D7, 30, 100 and 12 month after transplant.

  6. efficiency of chelation [ Time Frame: 3 and 16 months ]
    the effect of chelation will be assessed at 3 month after inclusion for all patient and post transplant by measuring Serum ferritin level

  7. number of patients with adverse events grade III and IV as assessed by CTCAE v4.0 [ Time Frame: 36 months ]
    comparison between patients with or without a donor for number of Grade III and IV toxicities (hematological and non-hematological) recorded according to NCI CTCAE criteria versions 4.0 during the 36 months

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   18 Years to 69 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  1. Signed Informed consent
  2. Classical IPSS intermediate 1 or low myelodysplastic syndrome associated with at least one poor prognosis feature:

    1. Intermediate or higher risk revised IPSS
    2. RBC transfusion dependent anemia and failure to 2 or more lines or therapy (including EPO, Lenalidomide or demethylating agent…)
    3. thrombocytopenia < 20 G/L requiring transfusion
    4. neutropenia < 0.5 G/L associated with severe infection (defined as requiring hospitalization)
  3. Patient aged ≥ 18 and < 70 years For young patients, 18-45 years, Fanconi disease and dyskeratosis should be ruled out
  4. Patient for whom a transplantation from a matched donor, (8/8 (HLA A, B, C, DRB1) identical at molecular level)unrelated donor or matched sibling), is considered irrespective of donor availability
  5. Performance status 0-2 on the Eastern Cooperative Oncology Group (ECOG) Scale (At time of screening)
  6. Negative pregnancy and adequate contraception (including in male patients wishing to father), if relevant.
  7. Wash-out of at least 30 days since a previous treatment with Vidaza, Lenalidomide, EPO or any other treatment inducing cytopenias.

Exclusion Criteria:

  1. MDS classified according to classical IPSS as intermediate 2 or High risk
  2. Transformation in Acute myeloid Leukemia (AML)
  3. Severe active infection or any other uncontrolled severe condition.
  4. Organ dysfunctions including the following

    • Hepatic : total bilirubin > 2 times upper limit of normal (ULN) (except moderate unconjugated hyperbilirubinemia due to intra medullary hemolysis or Gilbert syndrome) , alanine transaminase (ALT) and aspartate transaminase (AST) > 3xULN
    • Symptomatic respiratory chronic failure
    • Symptomatic cardiac failure
    • Renal clearance < 60ml/min
  5. Prior malignancy (except in situ cervix carcinoma, limited basal cell carcinoma, or other tumors if not active during the last 3 years)
  6. MDS with the following causal germline disease : Fanconi anemia, GATA2 related syndromes and telomere disorders

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT02757989

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Contact: Marie Robin, MD +33 1 42 49 96 60
Contact: Marie Sébert, MD +33 1 71 20 70 23

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CHU d'Amiens Recruiting
Amiens, France, 80054
Contact: Amandine Charbonnier, MD    +33 3 22 45 59 14   
Principal Investigator: Amandine Charbonnier, MD         
CHU d'Angers Recruiting
Angers, France, 49933
Contact: Sylvain Thépot, MD    +33 2 41 35 44 66   
Principal Investigator: Sylvain Thépot, MD         
Centre hospitalier Victor Dupouy Not yet recruiting
Argenteuil, France, 95100
Contact: Ahmad Aljijakli, MD    +33 1 34 23 22 39   
Principal Investigator: Ahmad Aljijakli, MD         
CHU Jean Minjoz Recruiting
Besançon, France, 25030
Contact: Eric Deconinck, MD, PHD    +33 3 81 66 83 51   
Principal Investigator: Eric Deconinck, MD, PHD         
Principal Investigator: Ana Berceanu, MD         
Hôpital Avicenne Not yet recruiting
Bobigny, France, 93009
Contact: Thorsten Braun, MD    +33 1 48 95 70 57   
Principal Investigator: Thorsten Braun, MD         
CHU de Haut Lévèque Recruiting
Bordeaux, France, 33604
Contact: Edouard Forcade, MD    +33 5 57 65 67 27   
Principal Investigator: Edouard Forcade, MD         
Principal Investigator: Sophie Dimicoli-Salazar, MD         
CHRU Côte de Nacre Recruiting
Caen, France, 14033
Contact: Stéphane Cheze, MD    +33 2 31 27 23 60   
Principal Investigator: Stéphane Cheze, MD         
Principal Investigator: Oumedaly Reman, MD         
CHU Estaing Recruiting
Clermont Ferrand, France, 63000
Contact: Jacques Olivier Bay, MD    +33 4 73 75 00 65   
Principal Investigator: Jacques Olivier Bay, MD         
Principal Investigator: Benoit De Renzis, MD         
CHSF Gilles de Corbeil Not yet recruiting
Corbeil-Essonnes, France, 91106
Contact: Stéphanie Haïat, MD    +33 1 61 69 61 69   
Principal Investigator: Stéphanie Haïat, MD         
Hôpital Henri Mondor Not yet recruiting
Créteil, France, 94010
Contact: Andrea Toma, MD    +33 1 49 81 20 60   
Principal Investigator: Andrea Toma, MD         
CHU de Grenoble Recruiting
Grenoble, France, 38043
Contact: Martin Carré, MD    +33 4 76 76 57 55   
Principal Investigator: Martin Carré, MD         
Principal Investigator: Sophie Park, MD, PHD         
CH Le Mans Not yet recruiting
Le Mans, France, 72037
Contact: Kamel Laribi, MD    +33 2 43 43 43 61   
Principal Investigator: Kamel Laribi, MD         
Hôpital Saint Vincent de Paul Recruiting
Lille, France, 59020
Contact: Laurent Pascal, MD, PHD    +33 3 20 87 45 32   
Principal Investigator: Laurent Pascal, MD, PHD         
Hôpital Huriez Recruiting
Lille, France, 59037
Contact: Ibrahim Yakoub-Agha, MD, PHD    +33 3 20 44 55 51   
Principal Investigator: Ibrahim Yakoub-Agha, MD, PHD         
Hôpital Dupuytren Not yet recruiting
Limoges, France, 87042
Contact: Pascal Turlure, MD    +33 5 55 05 80 39   
Principal Investigator: Marie-Pierre Gourin, MD         
Principal Investigator: Pascal Turlure, MD         
Centre hospitalier Lyon Sud Recruiting
Lyon, France, 69495
Contact: Hélène Labussière-Wallet, MD, PHD    +33 4 78 86 22 05   
Principal Investigator: Hélène Labussière-Wallet, MD, PHD         
Principal Investigator: Eric Wattel, MD, PHD         
GHEF, site de Meaux Not yet recruiting
Meaux, France, 77100
Contact: Loïc Fouillard, MD    +33 1 64 35 38 76   
Principal Investigator: Loïc Fouillard, MD         
CHRU de Montpellier Recruiting
Montpellier, France, 34295
Contact: Nathalie Fegueux, MD    +33 4 67 33 83 63   
Principal Investigator: Nathalie Fegueux, MD         
CHU de Nantes Recruiting
Nantes, France, 44093
Contact: Patrice Chevallier, MD    +33 2 40 08 33 33   
Principal Investigator: Patrice Chevallier, MD         
Principal Investigator: Pierre Peterlin, MD         
CHU de Nice Recruiting
Nice, France, 06202
Contact: Thomas Cluzeau, MD    +33 4 92 03 58 44   
Principal Investigator: Thomas Cluzeau, MD         
CHU de Nîmes Not yet recruiting
Nîmes, France, 30029
Contact: Stefan Wickenhauser, MD    +33 4 66 68 32 31   
Principal Investigator: Stefan Wickenhauser, MD         
Hôpital Saint Louis Recruiting
Paris, France, 75010
Contact: Marie Robin, MD    +33 1 42 49 96 60   
Principal Investigator: Marie Robin, MD         
Principal Investigator: Marie Sébert, MD         
Hôpital Pitié Salpétrière Not yet recruiting
Paris, France, 75013
Contact: Stéphanie Nguyen-Quoc, MD    +33 1 42 16 28 25   
Principal Investigator: Stéphanie Nguyen-Quoc, MD         
Hôpital Cochin Not yet recruiting
Paris, France, 75014
Contact: Lise Willems, MD    +33 1 58 41 26 70   
Principal Investigator: Lise Willems, MD         
Hôpital Necker Recruiting
Paris, France, 75015
Contact: Olivier Hermine, MD, PHD    +33 1 44 49 53 68   
Principal Investigator: Olivier Hermine, MD, PHD         
Principal Investigator: Felipe Suarez, MD         
CH Joffre Not yet recruiting
Perpignan, France, 66046
Contact: Laurence Sanhes, MD    +33 4 68 61 64 48   
Principal Investigator: Laurence Sanhes, MD         
CHU de Poitiers Recruiting
Poitiers, France, 86021
Contact: Natacha Maillard, MD    +33 5 48 44 44 44   
Principal Investigator: Jose Miguel Torregrosa Diaz, MD         
Principal Investigator: Natacha Maillard, MD         
CH René Dubos Not yet recruiting
Pontoise, France, 95300
Contact: Ioana-Dana Vaida, MD    +33 1 30 75 49 28   
Principal Investigator: Ioana-Dana Vaida, MD         
CHU de Reims Not yet recruiting
Reims, France, 51092
Contact: Chantal Himberlin, MD    +33 3 26 78 36 44   
Principal Investigator: Chantal Himberlin, MD         
Hôpital Pontchaillou Not yet recruiting
Rennes, France, 35033
Contact: Stanislas Nimubona, MD    +33 2 99 28 95 21   
Principal Investigator: Stanislas Nimubona, MD         
Centre Henri Becquerel Recruiting
Rouen, France, 76038
Contact: Aspasia Stamatoullas, MD    +33 2 32 08 22 88   
Principal Investigator: Aspasia Stamatoullas, MD         
Institut Curie Not yet recruiting
Saint-Cloud, France, 92210
Contact: Jacques Vargaftig, MD    +33 1 47 11 15 36   
Principal Investigator: Jacques Vargaftig, MD         
Institut de cancérologie Lucien Neuwirth Not yet recruiting
Saint-Priest-en-Jarez, France, 42271
Contact: Jérôme Cornillon, MD    +33 4 77 91 70 60   
Principal Investigator: Jérôme Cornillon, MD         
Hôpital civil Not yet recruiting
Strasbourg, France, 67091
Contact: Shanti Natarajan-Amé, MD    +33 3 88 11 67 28   
Principal Investigator: Shanti Natarajan-Amé, MD         
IUCT-Oncopole Recruiting
Toulouse, France, 31059
Contact: Anne Huynh, MD    +33 5 31 15 61 91   
Principal Investigator: Anne Huynh, MD         
Principal Investigator: Odile Beyne-Rauzy, MD, PHD         
Principal Investigator: Christian Recher, MD, PHD         
Hôpital Bretonneau Not yet recruiting
Tours, France, 37000
Contact: Emmanuel Gyan, MD, PHD    +33 2 47 25 87 78   
Principal Investigator: Emmanuel Gyan, MD, PHD         
Hôpital de Brabois Recruiting
Vandoeuvre les nancy, France, 54550
Contact: Maud D'Aveni, MD    +33 3 83 15 30 30   
Principal Investigator: Maud D'Aveni, MD         
Sponsors and Collaborators
Groupe Francophone des Myelodysplasies
Neovii Biotech
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Principal Investigator: Marie Robin, MD Saint-Louis Hospital, Paris, France

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Responsible Party: Groupe Francophone des Myelodysplasies Identifier: NCT02757989     History of Changes
Other Study ID Numbers: MDS-ALLO-RISK
2015-A00292-47 ( Other Identifier: IDRCB Number )
First Posted: May 2, 2016    Key Record Dates
Last Update Posted: May 27, 2019
Last Verified: May 2019
Keywords provided by Groupe Francophone des Myelodysplasies:
Low risk MDS
Additional relevant MeSH terms:
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Myelodysplastic Syndromes
Bone Marrow Diseases
Hematologic Diseases
Precancerous Conditions