Clinical trial · Observational
Study of Intracellular Nucleotide Pools Determination as Biomarker of the Efficacy of the Induction Treatment in Acute Myeloid Leukemia
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Treatment of acute myeloid leukemia (AML) consists in two main phases: induction and consolidation. Standard chemotherapy combination for induction treatment associates cytarabine (AraC), a nucleoside analog, and an anthracycline (most often daunorubucin). About 60-70% of patients achieved complete remission after this standard chemotherapy. As cytarabine competes with endogenous nucleotides to exert its activity, the aim of this protocol is to study in vivo the effect of intracellular nucleotide pools on the efficacy of the induction treatment. Thus, intracellular nucleotides levels will be determined in peripheral blood mononuclear cells of patients with acute myeloid leukemia before treatment, and results will be compared with the efficacy of the treatment. This parameter will be assessed by the achievement of complete remission.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Acute Myeloid Leukemia | Acute Myeloid Leukemia | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Biological analyses | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- acute myeloid leukemia patients
- description
- Patients over 18 years with acute myeloid leukemia
- interventionNames
- Biological: Biological analyses
Primary outcomes (1)
- measure
- Complete remission
- timeFrame
- 30 days
- description
- Primary endpoint will be the achievement of complete remission after induction treatment and bone marrow aplasia.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 65 Years
Show eligibility criteria text
Patients Inclusion Criteria: * age over 18 years * acute myeloid leukemia * standard induction chemotherapy with cytarabine and daunorubicin * patients who received the information and did not object to participate to the study Patients Exclusion Criteria: \- patients with acute myeloid leukemia 3 healthy volunteers Inclusion Criteria : * adults without known hematological disease, * adults who received the information and did not object to participate in the study healthy volunteers Exclusion Criteria : \- Volunteers with known hematological disease.
References
Publications (0)
Data not yet available