Summary
This phase III trial compares standard chemotherapy to therapy with liposome-encapsulated daunorubicin-cytarabine (CPX-351) and/or gilteritinib for patients with newly diagnosed acute myeloid leukemia with or without FLT3 mutations. Drugs used in chemotherapy, such as daunorubicin, cytarabine, and gemtuzumab ozogamicin, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. CPX-351 is made up of daunorubicin and cytarabine and is made in a way that makes the drugs stay in the bone marrow longer and could be less likely to cause heart problems than traditional anthracycline drugs, a common class of chemotherapy drug. Some acute myeloid leukemia patients have an abnormality in the structure of a gene called FLT3. Genes are pieces of DNA (molecules that carry instructions for development, functioning, growth and reproduction) inside each cell that tell the cell what to do and when to grow and divide. FLT3 plays an important role in the normal making of blood cells. This gene can have permanent changes that cause it to function abnormally by making cancer cells grow. Gilteritinib may block the abnormal function of the FLT3 gene that makes cancer cells grow. The overall goals of this study are, 1) to compare the effects, good and/or bad, of CPX-351 with daunorubicin and cytarabine on people with newly diagnosed AML to find out which is better, 2) to study the effects, good and/or bad, of adding gilteritinib to AML therapy for patients with high amounts of FLT3/ITD or other FLT3 mutations and 3) to study changes in heart function during and after treatment for AML. Giving CPX-351 and/or gilteritinib with standard chemotherapy may work better in treating patients with acute myeloid leukemia compared to standard chemotherapy alone.
Description
This Phase III clinical trial is comparing standard chemotherapy with newer treatment options for newly diagnosed acute myeloid leukemia (AML).
Who is the trial for?
Patients with newly diagnosed acute myeloid leukemia (AML). The trial is split into two groups based on a gene mutation:
Patients without a specific FLT3 gene mutation: Their treatment will be compared to standard chemotherapy.
Patients with a FLT3 gene mutation: They will receive a targeted drug, gilteritinib, in addition to their chemotherapy.
What are the new treatment options?
Option 1: CPX-351
This is a new version of two common chemotherapy drugs, daunorubicin and cytarabine, combined in a single package.
Option 2: Gilteritinib
This is a targeted therapy for patients whose AML has a specific gene abnormality called a FLT3 mutation.
The FLT3 gene can cause cancer cells to grow uncontrollably. Gilteritinib is designed to block this abnormal gene, stopping the cancer cells from growing.
What are the goals of the study?
The main goals are to find out if the new treatments are better than standard chemotherapy. Specifically, the trial will:
Compare CPX-351 to the standard daunorubicin and cytarabine to see which is more effective and has fewer side effects.
Assess the benefits and risks of adding gilteritinib to chemotherapy for patients with a FLT3 mutation.
Monitor heart function in patients during and after their treatment.
Principal Investigator
Study Coordinator
Research Contact
Lisa Luikart - lisa.luikart@vandaliahealth.org / 304-388-9944