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RECRUITINGOBSERVATIONAL

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

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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.

Who May Be Eligible (Plain English)

Who May Qualify: - 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 willing to sign a consent form). Who Should NOT Join This Trial: - 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) Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
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 data concerning them (signature of informed consent). 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 the protocol * Patients without health insurance (affiliation to a social security scheme)

Locations (20)

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