RecruitingNCT06891144

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


Sponsor

French Innovative Leukemia Organisation

Enrollment

1,000 participants

Start Date

Jan 6, 2015

Study Type

OBSERVATIONAL

Conditions

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

Min Age: 60 Years

Inclusion Criteria4

  • 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).

Exclusion Criteria4

  • 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)

Locations(27)

Angers CHU

Angers, France

Annecy CH

Annecy, France

Avignon CH

Avignon, France

Bayonne CH

Bayonne, France

Besançon CHU

Besançon, France

Brest CHU

Brest, France

CHU Estaing

Clermont-Ferrand, France

Colmar CH

Colmar, France

Grenoble CHU

Grenoble, France

Marseille IPC

Marseille, France

METZ-THIONVILLE CHR- Hôpital de Mercy

Metz, France

Montpellier - Chu Saint Eloi

Montpellier, France

Mulhouse Chu

Mulhouse, France

Nantes CHU

Nantes, France

Nimes CHU

Nîmes, France

Orléans CHU

Orléans, France

Paris Cochin, APHP

Paris, France

Perpignan CH

Perpignan, France

Bordeaux CHU

Pessac, France

Poitiers CHU

Poitiers, France

Reims CHU

Reims, France

Rennes CHU

Rennes, France

CHU de Saint-Etienne

Saint-Priest-en-Jarez, France

ICANS - Institut de cancérologie de strasbourg europe

Strasbourg, France

Toulouse - IUCT Oncopole - Service d'Hématologie

Toulouse, France

Tours CHU

Tours, France

Nancy CHU

Vandœuvre-lès-Nancy, France

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NCT06891144


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