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

Study acronym: CYTOK-AZA
StatusRecruiting
PhaseNot specified
Started2024-09-23
View on ClinicalTrials.gov ↗
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.

Amendment history 2 changes detected by DataLookout

2026-09-10
critical
Primary completion pushed: 2026-07-15 → 2028-07-15
2026-09-10
minor
Completion pushed: 2026-12-15 → 2029-12-15
Trial Details
NCT Number NCT06439199
Lead Sponsor Nantes University Hospital
Collaborators: Institut National de la Santé Et de la Recherche Médicale, France
Conditions Acute Myeloid Leukemia, Myelodysplastic Syndromes, Chronic Myelomonocytic Leukemia
Enrollment 60 participants
Start Date 2024-09-23
Primary Completion 2028-07-15 (estimated)
Study Completion 2029-12-15 (estimated)
Updated on ClinicalTrials.gov 2026-09-09