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ELN 2022 in MENAFC ( Middle Eastern or North Coast of Africa ) Patients With Newly AML

Not yet recruiting
Conditions
Leukemia, Myeloid
Interventions
Other: Middle Eastern or North Coast of Africa patients with newly AML
Registration Number
NCT06512610
Lead Sponsor
Centre Hospitalier Universitaire de Nice
Brief Summary

"In daily clinical practice, 2022 ELN guidelines were used to predict response to conventional treatment and to guide the need for allogenic stem cell transplantation. But, the team has to underline that ELN guidelines are mainly reflective of relatively young Caucasian patients. Few studies have compared 2017 and 2022 ELN in ethnicity cohorts to evaluate the potential prognostic value of this new criteria in these types of population. For example, with the 2022 ELN guidelines, the disease-free surviva) and the overall survival of African American \< 60 y.o were not statistically different between intermediate and adverse groups (p=0.30, p=0,46). There were not a significant difference between favorable and intermediate groups in DFS (p=0.42, p=0.42) respectively in African American and Hispanic patients or in OS (p=0.67) in Hispanic patients. Is the 2022 ELN applicable to all ethnic subgroups? To date, no studies have examined and validated its applicability in Middle Eastern or North Coast of Africa (MENAFC) patients."

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Newly diagnosed AML
  • At least 18 yo
  • MENAFC (Middle East ern of North Coast of Africa) patients with HLA HLA > 50%
  • ECOG performance status of 0,1,2,3"
Exclusion Criteria
  • Acute promyelocytic leukemia
  • Patients alive at the start of the study who did not receive study information or who objected to the collection of data"

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Middle Eastern or North Coast of Africa patients with newly AMLMiddle Eastern or North Coast of Africa patients with newly AMLValidation and refinement of the 2022 European LeukemiaNet genetic risk stratification of acute myeloid leukemia in MENAFC patients
Primary Outcome Measures
NameTimeMethod
Overall survival according to ELN 2022 genetic-risk group in comparison to ELN 2017Time from first administration of induction chemotherapy to death from any cause, assessed up to 01/01/2025

Patient alive or not. Patient alive at last follow-up were censored.

Secondary Outcome Measures
NameTimeMethod
Safety and toleranceTime from first administration of induction chemotherapy to death from any cause, assessed up to 01/01/2025

"Number of chemotherapy-related adverse events. Adverse events (AEs) were evaluated according to Common Terminology Criteria for Adverse Events classification: CTCAE (Version 4.0). Grade 1 = Mild - transient or mild discomfort; no limitation in activity; no medical intervention/therapy required

* Grade 2 = Moderate - mild to moderate limitation in activity, some assistance may be needed; no or minimal medical intervention/therapy required

* Grade 3 = Severe - marked limitation in activity, some assistance usually required; medical intervention/therapy required, hospitalization is possible

* Grade 4 = Life threatening - extreme limitation in activity, significant assistance required; significant medical intervention/therapy required, hospitalization or hospice care probable

* Grade 5 = Death "

Relapse free survival before alloHSCTTime from date of complete remission to date of relapse or death from any cause, assessed up to 01/01/2025

Patient who relapsed (confirmation with bone marow sample or MRD + Minimum residual Disease) / who died from any cause during the follow-up or patient with complete remission.

Risk group according to 2017 and 2022 ELNAt the diagnosis

Presence of genetic abnormalities resulting in 3 risks categories: favorable, Intermediate and Adverse

Complete remission ratesTime from first administration of induction chemotherapy to death from any cause, assessed up to 01/01/2025

complete remission rates %

Trial Locations

Locations (1)

CHU NICE

🇫🇷

Nice, Alpes Maritimes, France

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