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NCT04641910

Validation Study of a New Cytokine-based Dynamic Stratification Based on FLt3 Ligand Plasma Concentration Kinetic Profile and IL-6 Concentration During Induction of Acute Myeloid Leukemia

Sponsor: Nantes University Hospital

View on ClinicalTrials.gov

Summary

The investigators have recently demonstrated the strong impact in terms of survivals of Fms-like tyrosine kinase 3 ligand (FL) levels evaluated during intensive induction in acute myeloid leukemia (AML) patients. Indeed, three FL kinetic profiles were delineated: i) sustained increase of FL concentrations between day (D) 1 and D22 (FLI group, n=26, good-risk), ii) increase from D1 to D15, then decrease at D22 (FLD group, n=22, intermediate-risk) and iii) stagnation of low levels (\<1000 pg/mL, FLL group, n=14, high-risk). However, with longer follow-up, the investigators have observed that FLI and FLD shared similar outcomes while FLL sub-group kept a very bad prognostic. Because serum samples from this previous study (called the FLAM/FLAL study) had been frozen-stored, the investigators were able to conduct an ancillary study assessing the potential impact of the kinetics of 6 other cytokines: TNFalpha, stem-cell factor, IL-1beta, IL-6, IL-10 and granulocyte-monocyte colony-stimulating factor (GM-CSF).. Only Il-6 level at D22 (\< or \>15.5 pg/mL) was associated with outcome allowing to distinguish between higher and lower survivals within the combined FLI/FLD sub-group. A new prognostic risk-stratification can thus be proposed as follows: FLI/FLD with IL-6 \<15.5 pg/mL (favorable), FLI/FLD with IL-6 \>15.5 pg/mL (intermediate) and FLL (high-risk). The aim of this new FLAMVAL study is to validate prospectively in a larger and independent cohort this prognostic risk-stratification i.e. that kinetic profile of FLT3L plasma level from D1 to D22 and Il6 plasma level at day 22 during induction of AML patients are predictive of overall and disease free survivals. For that purpose, 201 newly diagnosed AML patients treated intensively in the 25 centres of the French Innovative Leukemia Organisation (FILO) will be included in the FLAMVAL study.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

201

Start Date

2021-06-08

Completion Date

2024-08-31

Last Updated

2026-04-16

Healthy Volunteers

No

Interventions

OTHER

No intervention

No intervention

Locations (25)

Strasbourg University Hospital

Strasbourg, Bas-Rhin, France

Paoli-Calmette Institute

Marseille, Bouches-du-Rhône, France

Besançon University Hospital

Besançon, Doubs, France

Brest University Hospital

Brest, Finistère, France

Nîmes University Hospital

Nîmes, Gard, France

Bordeaux University Hospital

Bordeaux, Gironde, France

Mulhouse Hospital Center

Mulhouse, Haut-Rhin, France

Toulouse University Cancer Institute

Toulouse, Haute-Garonne, France

Béziers Hospital Center

Béziers, Hérault, France

Montpellier University Hospital

Montpellier, Hérault, France

Rennes University Hospital

Rennes, Ille-et-Vilaine, France

Tours University Hospital

Tours, Indre-et-Loire, France

Grenoble University Hospital

Grenoble, Isère, France

Nantes University Hospital

Nantes, Loire-Atlantique, France

Angers University Hospital

Angers, Maine-et-Loire, France

Reims University Hospital

Reims, Marne, France

Nancy University Hospital

Nancy, Meurthe-et-Moselle, France

Mercy Regional Hospital

Metz, Moselle, France

Saint-Etienne University Hospital

Saint-Étienne-de-Montluc, Pays de la Loire Region, France

Clermont-Ferrand University Hospital

Clermont-Ferrand, Puy-de-Dôme, France

Basque coast hospital center

Bayonne, Pyrénées-Atlantiques, France

Saint-Jean Hospital Center

Perpignan, Pyrénées-Orientales, France

Lyon University Hospital

Lyon, Rhône, France

AP-HP Cochin Hospital

Paris, France

Poitiers University Hospital

Poitiers, France