Acute Myeloid Leukemia
Conditions
Interventions
Intervention type:
Name of intervention:
Dose form / Japanese Medical Device Nomenclature:
Route of administration / Site of application:
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Dosing frequency / Frequency of use:
Sponsors
Shuichi Miyawaki;
Division of Hematology, Tokyo Metropolitan Ohtsuka Hospital.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Untreated, de novo AML patients, who are positi ve for WT1-mRNA at diagnosis and without previous history of myelodysplastic syndrome.
Exclusion criteria
Exclusion criteria: AML cases who did not achieve complete remission after one-/two- course of remission-induction therapy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correlation between the comparison of WT1-mRNA of pre- with post-chemotherapy and 2-year relapse-free survival. | — |
Secondary
| Measure | Time frame |
|---|---|
| Correlation between characteristics of the patients and the change of WT1-mRNA level and survival. | — |
Countries
Japan
Contacts
Public ContactISHIYAMA, Ken
Tokyo Metropolitan Ohtsuka Hospital
Outcome results
None listed