400 Participants Needed

Monitoring for Acute Myeloid Leukemia and Myelodysplastic Syndrome

(MRD Trial)

MW
JL
Overseen ByJamie Littleton, MSN,RN,CCRC
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: University of Rochester
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to develop new tests to evaluate treatment effectiveness for individuals with Acute Myelogenous Leukemia (AML) or High Grade Myelodysplastic Syndrome (MDS). The goal is to identify patients at risk of disease recurrence after treatment. Participants sought are those being monitored or treated for AML or MDS who have not undergone strong chemotherapy or a bone marrow transplant in the past 3 months. This trial offers an opportunity to potentially enhance future treatment options for these conditions. As a Phase 2 trial, the research focuses on assessing treatment efficacy in an initial, smaller group, allowing participants to contribute to the development of effective therapies.

Why are researchers excited about this trial?

Researchers are excited about this clinical trial because it focuses on monitoring minimal residual disease (MRD) in patients with Acute Myelogenous Leukemia (AML) and High Grade Myelodysplastic Syndrome (MDS). This trial isn't about a new drug but rather a new technique for detecting MRD. Most treatments for AML and MDS rely on chemotherapy or stem cell transplants, which can be quite intense and have significant side effects. This new approach aims to precisely track even the smallest traces of cancer cells remaining after treatment, allowing for more tailored and timely interventions. By identifying MRD with greater accuracy, doctors can better predict relapses and potentially adjust treatments sooner, improving patient outcomes.

Who Is on the Research Team?

MW

Michael W Becker, MD

Principal Investigator

University of Rochester

Are You a Good Fit for This Trial?

Inclusion Criteria

Are being evaluated for the diagnosis and/or treatment of Acute Myelogenous Leukemia or High Grade myelodysplastic syndrome (defined as greater than 10 percent blasts on examination of the bone marrow aspirate).
Have not undergone prior cytotoxic therapy for acute myelogenous leukemia or High Grade myelodysplastic syndrome in the past 3 months other than hydroxyurea or Revlimid.
Have not previously received an allogeneic peripheral blood or bone marrow stem cell transplant for their disease.
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Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive therapy for AML or MDS, aiming to achieve remission

Varies

Monitoring

Special assays are performed to identify Minimal Residual Disease by targeting a minor population of malignant cells

2 years

Follow-up

Participants are monitored for safety and effectiveness after treatment

6 months

What Are the Treatments Tested in This Trial?

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Who Is Running the Clinical Trial?

University of Rochester

Lead Sponsor

Trials
883
Recruited
555,000+