RecruitingPhase 2Phase 3NCT02416388

Study to Improve OS in 18 to 60 Year-old Patients, Comparing Daunorubicin Versus High Dose Idarubicin Induction Regimens, High Dose Versus Intermediate Dose Cytarabine Consolidation Regimens, and Standard Versus MMF Prophylaxis of GvHD in Allografted Patients in First CR

Phase II/III Randomized Study to Improve Overall Survival in 18 to 60 Year-old Patients, Comparing Daunorubicin Versus High Dose Idarubicin Induction Regimens, High Dose Versus Intermediate Dose Cytarabine Consolidation Regimens, and Standard Versus Mycophenolate Mofetil Prophylaxis of Graft Versus Host Disease in Allografted Patients in First CR : a Backbone InterGroup-1 Trial


Sponsor

University Hospital, Angers

Enrollment

3,100 participants

Start Date

Jan 1, 2015

Study Type

INTERVENTIONAL

Conditions

Summary

This open label, multicenter phase II/III study with multiple randomization phases at differents stages of AML treatment (induction, consolidation and HSCT where applicable) is designed to improve OS in younger (18 to 60 year-old) patients, with AML risk-adapted patient strategies. Within the intermediate risk AML group, optimal GvHD prophylaxis following allogeneic SCT in first CR, after either myeloablative (MAC) or reduced intensity (RIC) conditioning, will also be evaluated. With an adaptative design, this clinical trial could test up to 3 novel AML agents of interest.


Eligibility

Min Age: 18 YearsMax Age: 61 Years

Plain Language Summary

Simplified for easier understanding

This trial tests new treatment approaches to improve survival for younger adults with acute myeloid leukemia (AML), a fast-growing blood cancer. **You may be eligible if...** - You are between 18 and 60 years old - You have been newly diagnosed with AML (either arising on its own or from a prior condition) - You have not received prior treatment for AML (temporary medication to control white blood cell counts is okay) - You are well enough to care for yourself with some limitations (ECOG score 3 or better) - Your liver and kidney function are adequate - You have had genetic testing of your leukemia cells done **You may NOT be eligible if...** - You have a severe uncontrolled infection - You have heart problems that prevent you from receiving certain chemotherapy drugs (anthracyclines) - You have already been treated for AML Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGIdarubicin

Induction chemotherapy : Idarubicin 9mg/m² /day, from D1 to D5 (IV, 30min) \+ cytarabine 200mg/m²/day from D1 to D7 (IV 24 h) Bone marrow aspirate on D15 : if medullary blasts rate \< 5% → G-CSF (5 μg/kg/day) until hematopoietic recovery (PNN ≥ 1 G/L).

DRUGDaunorubicin

Induction chemotherapy : Daunorubicin 90mg/m²/day, from D1 to D3 (IV, 30min) \+ cytarabine 200mg/m² /day from D1 to D7 (IV 24 h) Bone marrow aspirate on D15 : if medullary blasts rate \< 5% → G-CSF (5 μg/kg/day) until hematopoietic recovery (PNN ≥ 1 G/L).

DRUGHD Cytarabine

Consolidation chemotherapy course (s) : -High dose cytarabine: 3g/m² /12h on D1, D3 and D5 For all patients, G-CSF (5 μg/kg/day) : SC or IV (30 min) from D8 until hematopoietic recovery (PNN ≥ 1 G/L) Up to 3 consolidation courses, depending on the patient AML risk group

DRUGCyclosporine

GvHD prophylaxis post allogeneic SCT : -Cyclosporine : 3 mg/kg /day from D-1 (IV) or 6 mg/kg/day from D-3 (PO). Not to be stopped before D100

DRUGMethotrexate

GvHD prophylaxis post allogeneic SCT : -15 mg/m² on D+1 then 10 mg/m² on D+3, D+6 and D+11

DRUGMycophenolic acid (MPA)

GvHD prophylaxis post allogeneic SCT : * 720 mg BID from D0 to D+28 for HLA-identical siblings * 720 mg BID from D0 to D+45 for 10/10 HLA allele-matched unrelated donors

DRUGvosaroxin

Consolidation chemotherapy course (s) : -70 mg/m² on D1 and D4

DRUGID cytarabine

Consolidation chemotherapy course (s) : -Intermediate dose cytarabine: 1.5g/m² /12h on D1, D3 and D5 For all patients, G-CSF (5 μg/kg/day) : SC or IV (30 min) from D8 until hematopoietic recovery (PNN ≥ 1 G/L) Up to 3 consolidation courses, depending on the patient AML risk group

DRUGDexamethasone

Consolidation chemotherapy course (s) : -10 mg/12h on D1, D3 and D5

DRUGVenetoclax

Consolidation chemotherapy course (s) : Once RP2D has been determined from the results of the dose selection phase (phase 1), the optimal dose level retained for randomized phase 2 will be one of the following: * 100 mg/d on D1 to D8 (selection phase dose level 1) * or 200 mg/d on D1 to D8 (selection phase dose level 2) * or 400 mg/d on D1 to D8 (selection phase dose level 3) * or 400 mg/d on D1 to D14 (selection phase dose level 4)


Locations(56)

CH Amiens Hôpital Sud

Amiens, France

CHU Angers

Angers, France

CH Victor Dupouy

Argenteuil, France

Centre Hospitalier de la Côte Basque

Bayonne, France

Hôpital Jean Minjoz

Besançon, France

CH Beziers

Béziers, France

Hôpital Avicenne

Bobigny, France

CH Bordeaux

Bordeaux, France

Hôpital du Dr Duchenne

Boulogne-sur-Mer, France

Hôpital Morvan

Brest, France

CH Caen

Caen, France

Clinique du parc

Castelnau-le-Lez, France

Centre Hospitalier René Dubos

Cergy-Pontoise, France

HIA Percy

Clamart, France

CHU Estaing

Clermont-Ferrand, France

Centre Hospitalier Sud Francilien

Corbeil-Essonnes, France

Hôpital Henri Mondor

Créteil, France

CHU de Dijon

Dijon, France

CH Dunkerque

Dunkirk, France

Hôpital Michallon

Grenoble, France

CH Versailles

Le Chesnay, France

CH Lens

Lens, France

CHRU de Lille, Hôpital Huriez

Lille, France

Hôpital St Vincent de Paul

Lille, France

CHU de Limoges

Limoges, France

Centre Leon Berard (CLB)

Lyon, France

CH Lyon Sud

Lyon, France

Marseille La Conception

Marseille, France

Institut Paoli Calmettes

Marseille, France

CH Meaux

Meaux, France

CHR Metz Thionville_Hôpital de Mercy

Metz, France

Hôpital Saint Eloi

Montpellier, France

CH Mulhouse

Mulhouse, France

CH Hôtel Dieu

Nantes, France

Centre Antoine Lacassagne

Nice, France

CHU Nice

Nice, France

CHRU de Nîmes

Nîmes, France

Hôpital Cochin

Paris, France

Hôpital La Pitié Salpêtrière

Paris, France

Hôpital Necker Enfants Malades

Paris, France

Hôpital Saint Antoine

Paris, France

Hôpital St Louis

Paris, France

Centre Hospitalier Saint Jean

Perpignan, France

CHU de Poitiers

Poitiers, France

Hôpital Robert Debré

Reims, France

CH Pontchaillou

Rennes, France

Hopital Victor Provo

Roubaix, France

Centre Henri Becquerel

Rouen, France

Hôpital René Huguenin

Saint-Cloud, France

Institut de Cancérologie Lucien Neuwirth

Saint-Priest-en-Jarez, France

Hôpital Hautepierre

Strasbourg, France

IUCT Toulouse

Toulouse, France

CHU Bretonneau

Tours, France

CH Valenciennes

Valenciennes, France

Hôpitaux de Brabois_CHU Nancy

Vandœuvre-lès-Nancy, France

Institut de Cancérologie Gustave Roussy

Villejuif, France

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NCT02416388


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