RecruitingNCT06439199

Biological, Prospective Study Evaluating the Dosage of Plasma Cytokines Including the FLT3 Ligand and IL6 of Patients Treated With Non-intensive Chemotherapy

Single-center, Biological, Uncontrolled, Prospective Study Evaluating the Dosage of Plasma Cytokines Including the FLT3 (FMS-like Tyrosine Kinase 3) Ligand and IL6 With a View to Making a First Estimate of Their Prognostic Value on the Outcome of Patients Treated With Non-intensive Chemotherapy Such as Azacytidine for Acute Myelogenous Leukemia (AML), High Risk Myelodysplastic Syndrome (HR-MDS) or Chronic Myelomonocytic Leukemia (CMML)


Sponsor

Nantes University Hospital

Enrollment

60 participants

Start Date

Sep 23, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

There are 2 possible treatments for the treatment of Acute Myelogenous Leukemia (AML), high-risk myelodysplastic syndromes (HR-MDS) or chronic myelomonocytic leukemia (CMML): intensive curative chemotherapy , and for over-aged or co-morbid patients , non-intensive palliative chemotherapy with a hypomethylating agent (Azacytidine) associated or not with venetoclax. Pro-inflammatory cytokines and in particular IL-6 (Interleukin 6) seem to play a key role in the chemoresistance of solid cancers and AML : it would be associated with a poor prognosis of AML , would promote the proliferation of leukemic blasts , and would promote the progression of MDS to AML . In AML treated with intensive chemotherapy, researchers demonstrated that a particular kinetic profile of the FLT3 ligand and IL6 at day 22 could very significantly predict the survival of patients with AML . It therefore seems interesting to study the plasma cytokine profiles in patients with AML, HR-MDS or CMML treated non-intensively, and to see if researchers observe the same prognostic correlation as during intensive chemotherapy.


Eligibility

Min Age: 18 YearsMax Age: 99 Years

Plain Language Summary

Simplified for easier understanding

This study measures levels of certain proteins in the blood (cytokines, including FLT3 ligand and IL-6) in patients with blood cancers — specifically AML (acute myeloid leukemia), high-risk MDS (myelodysplastic syndrome), or CMML (a blood cancer involving both bone marrow and blood) — who are receiving a type of low-intensity chemotherapy called hypomethylating agents. The aim is to find markers that predict how well treatment works. **You may be eligible if...** - You are 18 or older - You have AML, high-risk MDS, or CMML receiving first-line or relapse treatment with a hypomethylating agent (with or without other drugs like venetoclax) - You are willing to participate and have signed a biocollection consent **You may NOT be eligible if...** - You do not have social security coverage - You are pregnant or unable to use contraception if you are of childbearing age - You are breastfeeding - You are a minor (under 18) - You are under legal guardianship 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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Locations(1)

Nantes University Hospital

Nantes, Loire-Atlantique, France

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NCT06439199


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