NCT04641910Completed
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
Source: ClinicalTrials.gov · Last updated 16 Apr 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 201 (actual)
- First submitted
- 18 Nov 2020
- Start date
- 8 Jun 2021
- Primary completion date
- 31 Aug 2024
- Lead sponsor
- Nantes University Hospital
- Diseases
- Acute myeloid leukemia
- NCT number
- NCT04641910
What you commit to
- Study type: Observational
- Participants enrolled: 201
- From 8 Jun 2021 to the primary completion date, 31 Aug 2024
- 25 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Patients diagnosed with Acute Promyelocytic Leukemia (AML-3)
- Adults under guardianship, subjects under protection.
Who the study is looking for
- Age \>= 18 years old
- Confirmed diagnosis of AML according to World Health Organization (WHO) 2016 classification (Arber et al., 2016)
- Non previously treated AML (first-line therapy)
- Patients eligible to standard 3+7 induction chemotherapy with a minimum of 3 days of daunorubicin at 45mg/m2/day or a minimum of 5 days of idarubicin at 8mg/m2/day and a minimum of 7 days of cytarabin at 100mg/m2/day
- Patients receiving any "third drug" combined to the "3+7" scheme, i.e. lomustine, corticotherapy, elthrombopag, gemtuzumab-ozogamycin, any FLT3 inhibitors… are eligible
- Patients receiving CPX-351 (Vyxeos ®) are eligible
- Patients requiring leukapheresis are eligible
- Signed informed consent
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (25)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Angers University Hospital Coordinator of this site? Confirm its status | Angers | France | Unknown status |
| Basque coast hospital center Coordinator of this site? Confirm its status | Bayonne | France | Unknown status |
| Besançon University Hospital Coordinator of this site? Confirm its status | Besançon | France | Unknown status |
| Béziers Hospital Center Coordinator of this site? Confirm its status | Béziers | France | Unknown status |
| Bordeaux University Hospital Coordinator of this site? Confirm its status | Bordeaux | France | Unknown status |
| Brest University Hospital Coordinator of this site? Confirm its status | Brest | France | Unknown status |
| Clermont-Ferrand University Hospital Coordinator of this site? Confirm its status | Clermont-Ferrand | France | Unknown status |
| Grenoble University Hospital Coordinator of this site? Confirm its status | Grenoble | France | Unknown status |
| Lyon University Hospital Coordinator of this site? Confirm its status | Lyon | France | Unknown status |
| Paoli-Calmette Institute Coordinator of this site? Confirm its status | Marseille | France | Unknown status |
| Mercy Regional Hospital Coordinator of this site? Confirm its status | Metz | France | Unknown status |
| Montpellier University Hospital Coordinator of this site? Confirm its status | Montpellier | France | Unknown status |
| Mulhouse Hospital Center Coordinator of this site? Confirm its status | Mulhouse | France | Unknown status |
| Nancy University Hospital Coordinator of this site? Confirm its status | Nancy | France | Unknown status |
| Nantes University Hospital Coordinator of this site? Confirm its status | Nantes | France | Unknown status |
| Nîmes University Hospital Coordinator of this site? Confirm its status | Nîmes | France | Unknown status |
| AP-HP Cochin Hospital Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| Saint-Jean Hospital Center Coordinator of this site? Confirm its status | Perpignan | France | Unknown status |
| Poitiers University Hospital Coordinator of this site? Confirm its status | Poitiers | France | Unknown status |
| Reims University Hospital Coordinator of this site? Confirm its status | Reims | France | Unknown status |
| Rennes University Hospital Coordinator of this site? Confirm its status | Rennes | France | Unknown status |
| Saint-Etienne University Hospital Coordinator of this site? Confirm its status | Saint-Étienne-de-Montluc | France | Unknown status |
| Strasbourg University Hospital Coordinator of this site? Confirm its status | Strasbourg | France | Unknown status |
| Toulouse University Cancer Institute Coordinator of this site? Confirm its status | Toulouse | France | Unknown status |
| Tours University Hospital Coordinator of this site? Confirm its status | Tours | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.