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NCT06891144Recruiting

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

Source: ClinicalTrials.gov · Last updated 24 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
1000 (estimated)
First submitted
14 Mar 2025
Start date
6 Jan 2015
Primary completion date
6 Jan 2030
Lead sponsor
French Innovative Leukemia Organisation
NCT number
NCT06891144

What you commit to

  • Study type: Observational
  • Planned participants: 1000
  • From 6 Jan 2015 to the primary completion date, 6 Jan 2030
  • 27 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with severe, uncontrolled infection at the time of inclusion
  • Patients with psychiatric or social disorders that will prevent compliance with the protocol

Other

  • Patients with AML 3
  • Patients without health insurance (affiliation to a social security scheme)

Who the study is looking for

  • 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).

Age in the registry: 60 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (27)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Angers - CHU
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AngersFranceRecruiting
Annecy - CH
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AnnecyFranceRecruiting
Avignon - CH
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AvignonFranceRecruiting
Bayonne - CH
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BayonneFranceRecruiting
Besançon - CHU
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BesançonFranceRecruiting
Brest - CHU
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BrestFranceRecruiting
CHU Estaing
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Clermont-FerrandFranceRecruiting
Colmar - CH
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ColmarFranceRecruiting
Grenoble - CHU
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GrenobleFranceRecruiting
Marseille IPC
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MarseilleFranceRecruiting
METZ-THIONVILLE CHR- Hôpital de Mercy
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MetzFranceRecruiting
Montpellier - Chu Saint Eloi
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MontpellierFranceRecruiting
Mulhouse Chu
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MulhouseFranceRecruiting
Nantes CHU
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NantesFranceRecruiting
Nimes Chu
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NîmesFranceRecruiting
Orléans CHU
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OrléansFranceRecruiting
Paris Cochin, APHP
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ParisFranceRecruiting
Perpignan CH
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PerpignanFranceRecruiting
Bordeaux - CHU
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PessacFranceRecruiting
Poitiers - CHU
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PoitiersFranceRecruiting
Reims - CHU
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ReimsFranceRecruiting
Rennes - CHU
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RennesFranceRecruiting
Chu de Saint Etienne
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Saint-Priest-en-JarezFranceRecruiting
ICANS - Institut de cancérologie de strasbourg europe
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StrasbourgFranceRecruiting
Toulouse - IUCT Oncopole - Service d'Hématologie
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ToulouseFranceRecruiting
Tours - CHU
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ToursFranceRecruiting
Nancy - CHU
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Vandœuvre-lès-NancyFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.