Epidemiological Study of a Prospective Cohort of Patients Aged 60 and Over Managed for Acute Myeloid Leukemia (AML) and Receiving Intensive Induction Therapy

Last updated: March 20, 2025
Sponsor: French Innovative Leukemia Organisation
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT06891144
FILObs_LAMSA 2013
  • Ages > 60
  • All Genders

Study Summary

This observational epidemiological study targets patients aged 60 and over with de novo or secondary acute myeloblastic leukemia suitable for intensive receive intensive induction therapy as defined by the group. The main aim of the study is to determine the epidemiological characteristics of AML patients, both clinically and biologically, and to correlate these to their outcome. The incidence of AML increases with age, exponentially after the age of 50, giving a median age at diagnosis of close to 70 years, with over half of patients half of patients are over 60 at diagnosis. The principle of treatment as in younger patients, is based on trying to achieve complete remission (CR). remission (CR). Observed complete remission rates range from 38 to 70%. Long-term survival of elderly subjects remains limited, at around 10 to 15%, despite the various types of consolidation tried out in recent years.

years. However, intensive chemotherapy remains the preferred option for initial treatment of these hematological diseases when general condition and comorbidities allow. As shown by Swedish registry studies, it is associated with improved life expectancy.

The proportion of patients who can receive intensive initial treatment is not well known in France, probably varies widely from one region to another, and certainly decreases with increasing age. Only the registry studies currently underway will enable us to assess this precisely.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • 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 dataconcerning them (signature of informed consent).

Exclusion

Exclusion Criteria:

  • 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 theprotocol

  • Patients without health insurance (affiliation to a social security scheme)

Study Design

Total Participants: 1000
Study Start date:
January 06, 2015
Estimated Completion Date:
January 06, 2031

Connect with a study center

  • Angers CHU

    Angers,
    France

    Active - Recruiting

  • Annecy CH

    Annecy,
    France

    Active - Recruiting

  • Avignon CH

    Avignon,
    France

    Active - Recruiting

  • Bayonne CH

    Bayonne,
    France

    Active - Recruiting

  • Besançon CHU

    Besançon,
    France

    Active - Recruiting

  • Brest CHU

    Brest,
    France

    Active - Recruiting

  • CHU Estaing

    Clermont-Ferrand,
    France

    Active - Recruiting

  • Colmar CH

    Colmar,
    France

    Active - Recruiting

  • Grenoble CHU

    Grenoble,
    France

    Active - Recruiting

  • Marseille IPC

    Marseille,
    France

    Active - Recruiting

  • METZ-THIONVILLE CHR- Hôpital de Mercy

    Metz,
    France

    Active - Recruiting

  • Montpellier - Chu Saint Eloi

    Montpellier,
    France

    Active - Recruiting

  • Mulhouse Chu

    Mulhouse, 68100
    France

    Active - Recruiting

  • Nantes CHU

    Nantes,
    France

    Active - Recruiting

  • Nimes CHU

    Nîmes,
    France

    Active - Recruiting

  • Orléans CHU

    Orléans, 45000
    France

    Active - Recruiting

  • Paris Cochin, APHP

    Paris,
    France

    Active - Recruiting

  • Perpignan CH

    Perpignan,
    France

    Active - Recruiting

  • Bordeaux CHU

    Pessac,
    France

    Active - Recruiting

  • Poitiers CHU

    Poitiers,
    France

    Active - Recruiting

  • Reims CHU

    Reims,
    France

    Active - Recruiting

  • Rennes CHU

    Rennes,
    France

    Active - Recruiting

  • CHU de Saint-Etienne

    Saint-Priest-en-Jarez,
    France

    Active - Recruiting

  • ICANS - Institut de cancérologie de strasbourg europe

    Strasbourg,
    France

    Active - Recruiting

  • Toulouse - IUCT Oncopole - Service d'Hématologie

    Toulouse,
    France

    Active - Recruiting

  • Tours CHU

    Tours,
    France

    Active - Recruiting

  • Nancy CHU

    vandoeuvre les Nancy,
    France

    Active - Recruiting

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