Skip to content

A Study of c-Kit Mutation as MRD in Acute Myeloid Leukemia

Absolute Quantification of c-Kit Mutation as MRD in Acute Myeloid Leukemia: a Prospective Observational Study

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06116318
Enrollment
0
Registered
2023-11-03
Start date
2023-11-01
Completion date
2026-11-01
Last updated
2026-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

C-KIT Mutation

Keywords

Acute myeloid leukemia, c-Kit mutation, MRD

Brief summary

C-Kit is involved in an essential pathway of disease occurrence and is closely related to the poor prognosis of patients. However, the clinical significance of c-Kit mutation as molecular MRD monitoring is still unclear. What are the differences and advantages of using c-Kit mutation as MRD in prognostic assessment compared with other MRDs (MFC or RUNX1::RUNX1T1) widely used today? Existing data suggest that patients with one positive and one negative MRD results obtained by two different techniques have a higher risk of recurrence than patients with two negative MRD results but a lower risk of recurrence than patients with two positive MRD results. Therefore, can combining multiple MRD markers, including c-Kit mutations, overcome the shortcomings of a single molecular marker as MRD monitoring? Therefore, this project intends to confirm the clinical significance of quantitative detection of c-Kit mutation as MRD in acute myeloid leukemia.

Interventions

None listed

Sponsors

Institute of Hematology & Blood Diseases Hospital, China
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
14 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients who meet the diagnostic criteria(WHO 2016 criteria) of AML and have c-Kit D816 mutation. And receive treatment.

Exclusion criteria

Patients with other factors which were considered unsuitable to participate in the study by the investigators

Design outcomes

Primary

MeasureTime frameDescription
CIRWithin 5 years after treatmentcumulative incidence of recurrence

Secondary

MeasureTime frameDescription
OSWithin 5 years after treatmentOverall Survival Rate
RFSWithin 5 years after treatmentRelapse-free survival

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 14, 2026