RecruitingPhase 2NCT07023588

Study on Optimizing the Treatment of Patients With Acute Myeloid Leukemia Based on Early Peripheral Blood Minimal Residual Disease

A Multicenter, Open-label, Prospective, Randomized Controlled Study to Optimize the Treatment of Patients With Acute Myeloid Leukemia Based on Early Peripheral Blood Minimal Residual Disease


Sponsor

Yehui Tan

Enrollment

70 participants

Start Date

Jun 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

A multicenter, open-label, prospective, randomized controlled study to optimize the treatment of patients with acute myeloid leukemia based on early peripheral blood minimal residual disease


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether checking for cancer cells in the blood early during treatment can help doctors adjust chemotherapy to improve outcomes for newly diagnosed patients with acute myeloid leukemia (AML), a type of blood cancer. **You may be eligible if...** - You are 18 or older - You have been newly diagnosed with AML (confirmed by bone marrow tests) - You have had full diagnostic testing including genetic and chromosomal analysis - Your blood test on day 6 of treatment shows at least 1% blast cells (immature cancer cells) - Your kidney and liver function are adequate - Your doctor has determined you are suitable for standard chemotherapy **You may NOT be eligible if...** - You have a specific subtype of AML called acute promyelocytic leukemia (APL) - Your AML has mixed features (mixed phenotype acute leukemia) - Your cancer has spread to the brain or nervous system - You have cancer outside the bone marrow (extramedullary disease) - You have severe kidney or liver dysfunction Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGVenetoclax

Patients identified with a suboptimal response to chemotherapy based on minimal residual disease (MRD) levels in peripheral blood on Day 6 will initiate venetoclax therapy added on Day 8, administered for 7 days.


Locations(1)

The First Hospital of Jilin University

Changchun, Jilin, China

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NCT07023588


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