Actively Recruiting
Epidemiological Study of a Prospective Cohort of Patients Aged 60 and Over Managed for Acute Myeloid Leukemia (AML) and Receiving Intensive Induction Therapy
Led by French Innovative Leukemia Organisation · Updated on 2025-03-24
1000
Participants Needed
27
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying patients aged 60 and older who have newly diagnosed or secondary acute myeloblastic leukemia (AML) and are suitable for intensive induction therapy. The study aims to understand the clinical and biological characteristics of AML in these patients and how these relate to their outcomes. AML is more common with increasing age, especially after 50, with a median diagnosis age near 70. Despite treatments aiming for remission, long-term survival in elderly patients remains limited. This observational study follows patients who receive intensive chemotherapy as their initial treatment when their general health and other conditions allow. The study collects data on the patients' initial AML characteristics, the first line of AML treatment they receive, and tracks their overall survival up to five years. The study does not test new treatments but monitors standard intensive therapy outcomes. Participants will have their disease characteristics described within three months of diagnosis, their initial treatment recorded over 12 months, and their overall survival monitored for five years. The study involves collecting clinical and biological data to better understand AML in older adults. Participation includes agreement to data collection and follow-up to assess outcomes and survival over several years.
CONDITIONS
Brief Title
Epidemiological Study of a Prospective Cohort of Patients Aged 60 and Over Managed for Acute Myeloid Leukemia (AML) and Receiving Intensive Induction Therapy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 60 and over
- Patients with previously untreated de novo or secondary AML
- Patients suitable for standard intensive treatment
- Patients who have read the information document and agreed to the collection of data concerning them (signature of informed consent)
You will not qualify if you...
- Patients with AML 3
- Patients with severe, uncontrolled infection at the time of inclusion
- Patients with psychiatric or social disorders that will prevent compliance with the protocol
- Patients without health insurance (affiliation to a social security scheme)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 12 months
Participants are observed to describe the initial characteristics of Acute Myeloid Leukemia and track first line AML treatment received.
Duration - 5 years
Participants are followed to characterize overall survival over an extended period.
Trial Site Locations
Total: 27 locations
1
Angers CHU
Angers, France
Actively Recruiting
2
Annecy CH
Annecy, France
Actively Recruiting
3
Avignon CH
Avignon, France
Actively Recruiting
4
Bayonne CH
Bayonne, France
Actively Recruiting
5
Besançon CHU
Besançon, France
Actively Recruiting
6
Brest CHU
Brest, France
Actively Recruiting
7
CHU Estaing
Clermont-Ferrand, France
Actively Recruiting
8
Colmar CH
Colmar, France
Actively Recruiting
9
Grenoble CHU
Grenoble, France
Actively Recruiting
10
Marseille IPC
Marseille, France
Actively Recruiting
11
METZ-THIONVILLE CHR- Hôpital de Mercy
Metz, France
Actively Recruiting
12
Montpellier - Chu Saint Eloi
Montpellier, France
Actively Recruiting
13
Mulhouse Chu
Mulhouse, France, 68100
Actively Recruiting
14
Nantes CHU
Nantes, France
Actively Recruiting
15
Nimes CHU
Nîmes, France
Actively Recruiting
16
Orléans CHU
Orléans, France, 45000
Actively Recruiting
17
Paris Cochin, APHP
Paris, France
Actively Recruiting
18
Perpignan CH
Perpignan, France
Actively Recruiting
19
Bordeaux CHU
Pessac, France
Actively Recruiting
20
Poitiers CHU
Poitiers, France
Actively Recruiting
21
Reims CHU
Reims, France
Actively Recruiting
22
Rennes CHU
Rennes, France
Actively Recruiting
23
CHU de Saint-Etienne
Saint-Priest-en-Jarez, France
Actively Recruiting
24
ICANS - Institut de cancérologie de strasbourg europe
Strasbourg, France
Actively Recruiting
25
Toulouse - IUCT Oncopole - Service d'Hématologie
Toulouse, France
Actively Recruiting
26
Tours CHU
Tours, France
Actively Recruiting
27
Nancy CHU
Vandœuvre-lès-Nancy, France
Actively Recruiting
Research Team
A
Ariane Mineur
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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