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Minimal residual disease in peripheral blood compared to bone marrow in patients treated for acute myeloid leukemia

Conditions
Acute myeloid leukemia
Registration Number
NL-OMON25015
Lead Sponsor
one
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
151
Inclusion Criteria

Patient with:
- a diagnosis of AML and related precursor neoplasms according to WHO 2008 classification (excluding acute promyelocytic leukemia) including secondary AML (after an antecedent hematological disease (e.g. MDS) and therapy-related AML), or
- acute leukemia’s of ambiguous lineage according to WHO 2008 or
- a diagnosis of refractory anemia with excess of blasts (MDS) and IPSS-R score > 4.5.
Treated according to HOVON clinical trials with intensive chemotherapy;
Age 18 yr or older;
A bone marrow aspiration has been scheduled;
WHO performance status 0, 1 or 2;
Written informed consent.

Exclusion Criteria

Pregnant or lactating females;
Unwilling or not capable to use effective means of birth control.

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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