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Phase III Study Comparing GVHD Prophylaxis With ATG-thymoglobulin to ATLG-grafalon in Elderly Patients With Acute Myeloid Leukemia or Myelodysplasic Syndrome and Receiving an Allogeneic Hematopoietic Stem Cell Transplantation With a 10/10 HLA Matched Unrelated Donor Following a Reduced Intensity Conditioning Regimen by Fludarabine-treosulfan

Status: Recruiting
Location: See all (28) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains the only curative therapy in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). Most of the patients requiring an allo-HSCT are above 50 years of age and are transplanted with a reduced intensity conditioning (RIC) regimen. The optimal RIC and Graft Versus Host Disease (GVHD) prophylaxis regimen allowing a good control of the disease while preventing GVHD remains to be determined for elderly patients. A phase III trial comparing the conventional RIC fludarabine-busulfan 2 days to fludarabine-treosulfan demonstrated an advantage for the flu-treosulfan arm in terms of event free survival (EFS), that should therefore be considered as the new standard of RIC regimen for AML and MDS. GVHD prevention has a crucial role in post-transplant outcomes by potentially interfering with the graft-versus-leukemia (GVL) effect and immune reconstitution. Anti-thymocyte globulins (ATG) are recommended to reduce the risk of acute and chronic GVHD in transplants performed with matched unrelated donors. However, the optimal type of ATG between the 2 approved brands (ATG-thymoglobulin and ATLG-grafalon) displaying distinct characteristics and the optimal dose of ATG are still unknown. In a retrospective study of patients transplanted mainly with RIC with matched related and unrelated donors for haematological malignancies, Anti-T lymphocyte globulin (ATLG) was associated with a reduction of grade II-IV acute GVHD in comparison to ATG without increasing the incidence of relapse. This phase III randomised study propose to compare GVHD prevention with ATG versus ATLG in AML and MDS patients above 50 years of age transplanted with a matched unrelated donor following a fludarabine-treosulfan RIC, with the hypothesis that ATLG would better control GVHD in this population of patients thus limiting the risk of morbidity and mortality of the procedure.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Maximum Age: 70
Healthy Volunteers: f
View:

⁃ Age ≥ 50 and ≤ 70 years

⁃ Patient between 50 and 55 years should be unfit for a myeloblative conditioning (SORROR score ≥2)

⁃ AML requiring allogeneic stem cell transplantation (intermediate or high-risk AML) in complete cytologic response (CR1 or above) or MDS requiring allogeneic stem cell transplantation (IPSS≥ 1.5 or IPSS-R \> 4.5 or IPSS-R \> 3-4.5 with risk features \[rapide blast increase, life-threatening neutropenia (\<0.3 G/L) or thrombopenia (\<30G/L) or high transfusion needs (\>2/month for 6 months)\]

⁃ Without an HLA matched related donor

⁃ Having an identified matched HLA 10/10 unrelated donor

⁃ With usual criteria for HSCT:

∙ ECOG performans status ≤ 2

‣ No severe and uncontrolled infection

‣ Cardiac left ventricular ejection fraction ≥50%

‣ Lung DLCO \> 40%

‣ Adequate organ function: ASAT and ALAT ≤ 3N, total bilirubin ≤ 2N, creatinine clearance ≥ 50 mL/min (except if those abnormalities are linked to the hematological disease)

⁃ With health insurance coverage

⁃ Having signed a written informed consent

⁃ Contraception methods must be prescribed during all the duration of the research

• NB: The authorized contraceptive methods are:

• For women of childbearing age and in absence of permanent sterilization: oral, intravaginal or transdermal combined hormonal contraception, oral, injectable or transdermal progestogen-only hormonal contraception, intrauterine hormonal releasing system (IUS), sexual abstinence (only if this the preferred and usual lifestyle of the participants).

• For man in absence of permanent sterilization: sexual abstinence, condoms

Locations
Other Locations
France
CHU Amiens
RECRUITING
Amiens
CHU Angers
RECRUITING
Angers
CHU Besançon
RECRUITING
Besançon
CHU Bordeaux
RECRUITING
Bordeaux
CHU Brest
RECRUITING
Brest
CHU Caen
RECRUITING
Caen
CHU Clermont-Ferrand
RECRUITING
Clermont-ferrand
Hôpital Henri Mondor AP-HP
NOT_YET_RECRUITING
Créteil
CHU Grenoble
RECRUITING
Grenoble
CHU Lille
RECRUITING
Lille
CHU Limoges
RECRUITING
Limoges
CHU Lyon Sud
RECRUITING
Lyon
IPC Marseille
RECRUITING
Marseille
CHU Montpellier
RECRUITING
Montpellier
CHRU Nancy
RECRUITING
Nancy
CHU Nantes
RECRUITING
Nantes
CHU Nice
RECRUITING
Nice
Hôpital La Pitié Salpêtrière AP-HP
RECRUITING
Paris
Hôpital Necker AP-HP
RECRUITING
Paris
Hôpital Saint Louis AP-HP
RECRUITING
Paris
Hôpital Saint-Antoine AP-HP
RECRUITING
Paris
CHU Poitiers
RECRUITING
Poitiers
CHU Rennes
RECRUITING
Rennes
CHU Saint Etienne
RECRUITING
Saint-etienne
CHRU Strasbourg
RECRUITING
Strasbourg
Oncopole Toulouse
RECRUITING
Toulouse
CHRU Tours
NOT_YET_RECRUITING
Tours
Institut Gustave Roussy
RECRUITING
Villejuif
Contact Information
Primary
Régis Peffault de Latour, Pr
regis.peffaultdelatour@aphp.fr
+33142385073
Backup
Jérôme Lambert, Dr
jerome.lambert@u-paris.fr
+33142499742
Time Frame
Start Date: 2023-11-28
Estimated Completion Date: 2028-11-28
Participants
Target number of participants: 324
Treatments
Active_comparator: Anti-T lymphocyte globulin (ATLG)
Active_comparator: Anti Thymocyte Globulins (ATG)
Sponsors
Leads: Assistance Publique - Hôpitaux de Paris

This content was sourced from clinicaltrials.gov

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