Actively Recruiting

Age: 60Years +
All Genders
ID06891144

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

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

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)
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

Duration - 12 months

Participants are observed to describe the initial characteristics of Acute Myeloid Leukemia and track first line AML treatment received.

Long-term Monitoring

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

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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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