Acute Myeloid Leukemia
Conditions
Keywords
Prognosis of Acute myeloblastic leukemia
Brief summary
AML in adults represents a group of heterogeneous diseases; the prognosis remains poor despite significant therapeutic advances in recent years. In order to optimize patient care, it is necessary to have real life data that exhaustively reports on the patients treated in our department. The objective of this study is: * To describe the AML treated within the hematology department * To optimize the management of patients with AML.
Detailed description
Current state of knowledge: Acute myeloblastic leukemia are the most common leukemias in adults. This pathology is very heterogeneous. It has a poor prognosis despite numerous therapeutic advances. The lack of randomized clinical trials can make certain treatment decisions difficult. In addition, patients with comorbidities or the elderly are most often excluded from these trials even though they represent a significant proportion of new diagnoses. Objectives: Primary objective Evaluate the overall survival of adult patients treated for AML in our hematology department at Saint-Antoine Hospital. Secondary objectives * Evaluate early mortality at 30 days and 60 days post-induction * Evaluate the CR/CRi rate after induction * Evaluate the toxicity of the treatments * Evaluate the relapse-free survival time * Assess the prognostic value of JC-1 at diagnosis * Evaluate the proportion of patients eligible for intensive treatment and/or allograft * Evaluate the side effects of the treatments undertaken * Describe the molecular and cytogenetic characteristics of hemopathies at diagnosis and at relapse Duration of study: Retrospective cohort (cohort A): patients diagnosed between junuary1,2010 and May 30,2022 Prospective cohort (cohort B): patients diagnosed between June 1, 2022 and December 31, 2023. A follow-up of 2 years will be necessary after the end of treatment. The end of follow-up is estimated at December 2025 for the entire cohort. Data collection: Collection of clinical and biological data in the patient's medical file via the Orbis software Population: Adult patients treated for AML at Saint-Antoine hospital
Interventions
None listed
Sponsors
Assistance Publique - Hôpitaux de Paris
Study design
Observational model
COHORT
Time perspective
OTHER
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age :18 years and older * Patients with AML * Non objection to research
Exclusion criteria
* Minor patients * Acute promyelocytic leukemia (AML3)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Overall survival | 2 years after diagnosis |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Side effects | 24 months | according to the CTCAE v5.0 classification |
| the rate of patients receiving intensive treatment | 24 months | — |
| Overall survival | 6 months after diagnosis | — |
| Cytological remission rate | after the phase of induction up to 24 months | — |
| Incomplete cytological remission rate | after the phase of induction up to 24 months | — |
| Leukemia free survival rate | 24 months | — |
Countries
France
Contacts
Primary ContactAlexis GENTHON, MD
Outcome results
None listed