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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
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

Full criteria on ClinicalTrials.gov

Sites (25)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Angers University Hospital
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AngersFranceUnknown status
Basque coast hospital center
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BayonneFranceUnknown status
Besançon University Hospital
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BesançonFranceUnknown status
Béziers Hospital Center
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BéziersFranceUnknown status
Bordeaux University Hospital
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BordeauxFranceUnknown status
Brest University Hospital
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BrestFranceUnknown status
Clermont-Ferrand University Hospital
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Clermont-FerrandFranceUnknown status
Grenoble University Hospital
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GrenobleFranceUnknown status
Lyon University Hospital
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LyonFranceUnknown status
Paoli-Calmette Institute
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MarseilleFranceUnknown status
Mercy Regional Hospital
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MetzFranceUnknown status
Montpellier University Hospital
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MontpellierFranceUnknown status
Mulhouse Hospital Center
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MulhouseFranceUnknown status
Nancy University Hospital
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NancyFranceUnknown status
Nantes University Hospital
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NantesFranceUnknown status
Nîmes University Hospital
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NîmesFranceUnknown status
AP-HP Cochin Hospital
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ParisFranceUnknown status
Saint-Jean Hospital Center
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PerpignanFranceUnknown status
Poitiers University Hospital
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PoitiersFranceUnknown status
Reims University Hospital
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ReimsFranceUnknown status
Rennes University Hospital
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RennesFranceUnknown status
Saint-Etienne University Hospital
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Saint-Étienne-de-MontlucFranceUnknown status
Strasbourg University Hospital
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StrasbourgFranceUnknown status
Toulouse University Cancer Institute
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ToulouseFranceUnknown status
Tours University Hospital
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ToursFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.