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
- Registration Number
- NCT06083129
- Lead Sponsor
- Assistance Publique - Hôpitaux de Paris
- Brief 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, we observed that 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.
In this phase III randomised study, we 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 324
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Age ≥ 50 and ≤ 70 years
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Patient between 50 and 55 years should be unfit for a myeloblative conditioning (SORROR score ≥2)
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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)]
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Without an HLA matched related donor
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Having an identified matched HLA 10/10 unrelated donor
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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)
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With health insurance coverage
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Having signed a written informed consent
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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
- Cancer in the last 5 years (except basal cell carcinoma of the skin or "in situ" carcinoma of the cervix)
- Uncontrolled infection
- Seropositivity for HIV or HTLV-1 or active hepatitis B or C
- Yellow fever vaccine and all others live virus vaccines within 2 months before transplantation
- Heart failure according to NYHA (II or more) or Left ventricular ejection fraction < 50%.
- Lung DLCO ≤ 40%
- Preexisting acute hemorrhagic cystitis
- Renal failure with creatinine clearance < 50ml / min
- Pregnancy (β-HCG positive) or breast-feeding
- Patients with any debilitating medical or psychiatric illness, which would preclude the realization of the SCT or the understanding of the protocol
- Patient under state medical aid
- Patient under legal protection (protection of the court, or in curatorship or guardianship).
- For Grafalon: Hypersensitivity to the active substance or to any of the excipients
- For Thymoglobulin: Hypersensitivity to rabbit proteins or to any of the excipients
- Participation in other interventional clinical trials
- Any contraindication mentioned in the SmPC of all auxiliary medicinal products planned to be used in the trial: cyclosporine, mycophenolate mofetil, fludarabine, treosulfan
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Anti-T lymphocyte globulin (ATLG) Grafalon - Anti Thymocyte Globulins (ATG) Thymoglobulin -
- Primary Outcome Measures
Name Time Method Incidence of grade II-IV acute Graft Versus Host Disease (GVHD) according to the Mount Sinai Acute GVHD International Consortium (MAGIC) classification At day 100 post-transplantation Acute GVHD MAGIC classification permit to diagnose and score the severity of acute GVHD.
MAGIC score varies from Grade 0 to Grade 4. The higher the score the more severe the damage.
- Secondary Outcome Measures
Name Time Method T, B, NK, regulatory T cell and gammaglobulin levels in the peripheral blood 24 months after transplantation Immune reconstitution
Number of patients with at least 3 consecutive days with neutrophils > 0.5 G/L and platelets > 20 G/L Up to 24 months Hematopoietic recoveries
Percentage of chimerism 12 months after transplantation Incidence of chronic GVHD 24 months after transplantation Incidence of chronic GVHD according to National Institutes of Health (NIH) classification. The gradation of chronic GvHD is defined by the number and score of affected organ. The higher the score of each organ and the higher the number of organs affected, the more severe the damage.
Progression free survival 24 months after transplantation Health-related Quality of life 12 months after transplantation Assessed by using the FACT-BMT-v4 questionnaire. It is a 50 items score. The score varies between 0 to 200. The higher the score the lower the quality of life.
Number of severe infections 12 months after transplantation Severe infections correspond to grade 3-4 according to Common Terminology Criteria for Adverse Events
Incidence of CytoMegaloVirus (CMV) reactivation 12 months after transplantation Overall survival 24 months after transplantation Incidence and severity of veino-occlusive disease (VOD) 100 days after transplantation Incidence of grade I acute GVHD Up to 24 months Treatments for acute GVHD will be described : first line treatment, response to steroids, treatment courses for refractory acute GVHD
Incidence of relapse 24 months after transplantation Relapse will be defined by the reappearance of leukemic cells or MDS features after allo-HSCT in the bonne marrow (cytology +/- cytogenetic analysis from bone marrow aspiration) or extra-medullary sites (proven by a biopsy).
Incidence of Ebstein Barr Virus (EBV) reactivation 12 months after transplantation Non-relapse mortality 24 months after transplantation GVHD and relapse free survival (GRFS) Up to 24 months after transplantation Defined by being alive without disease relapse and without having developed acute grade III-IV or severe chronic GVHD
Lymphocyte counts on standard blood counts before conditioning 7 days before transplantation Number of days of hospitalization for the transplant and after the hospitalization for transplantation related complications Up to 12 months after transplantation Number of late acute GvHD, overlap syndromes and chronic GvHD from day 100 to day 120 after transplantation