Evaluating c-Kit Mutation as a Marker in Acute Myeloid Leukemia

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

Observational Institute of Hematology & Blood Diseases Hospital, China · NCT06116318

This study is testing if c-Kit mutations can help doctors better track and predict the risk of relapse in patients with acute myeloid leukemia by comparing it to other monitoring methods.

Quick facts

Study typeObservational
Enrollment50 (estimated)
Ages14 Years and up
SexAll
SponsorInstitute of Hematology & Blood Diseases Hospital, China Academic / other
Locations1 site (Tianjin)
Trial IDNCT06116318 on ClinicalTrials.gov

What this trial studies

This observational study aims to assess the clinical significance of c-Kit mutations as a molecular marker for minimal residual disease (MRD) in patients with acute myeloid leukemia (AML). It will compare the prognostic value of c-Kit mutations against other established MRD monitoring techniques. The study seeks to determine if combining multiple MRD markers, including c-Kit mutations, can provide a more accurate risk assessment for recurrence in AML patients. By analyzing the relationship between different MRD results, the study hopes to enhance the understanding of c-Kit mutations in disease monitoring.

Who should consider this trial

Good fit: Ideal candidates for this study are patients diagnosed with acute myeloid leukemia who have the c-Kit D816 mutation.

Not a fit: Patients with other mutations or those not meeting the diagnostic criteria for AML may not benefit from this study.

Why it matters

Potential benefit: If successful, this study could improve the accuracy of MRD monitoring in AML, leading to better patient management and outcomes.

How similar studies have performed: While the specific approach of using c-Kit mutations as MRD monitoring is novel, existing studies have shown the importance of multiple MRD markers in assessing recurrence risk.

Eligibility criteria

Show full inclusion / exclusion criteria
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

Where this trial is running

Tianjin

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions C-KIT MutationAcute myeloid leukemiac-Kit mutationMRD
Last reviewed 2026-06-09 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.