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
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 type | Observational |
|---|---|
| Enrollment | 50 (estimated) |
| Ages | 14 Years and up |
| Sex | All |
| Sponsor | Institute of Hematology & Blood Diseases Hospital, China Academic / other |
| Locations | 1 site (Tianjin) |
| Trial ID | NCT06116318 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
- Institute of Hematology & Blood Diseases Hospital — Tianjin, China (Recruiting)
Study contacts
- Study coordinator: Hui Wei, Doctor
- Email: weihui@ihcams.ac.cn
- Phone: 13132507161
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.