New experimental drug may be game-changer for acute myeloid leukemia
Clinical trials for a new experimental drug, CPX-351, to treat acute myeloid leukemia (AML) are very promising, according to researchers. Patients treated with CPX-351, a combination of the chemotherapeutic drugs cytarabine and daunorubicin, are showing better responses than patients treated with the standard drug formulation.
"Acute myeloid leukemia is an aggressive blood cancer with very low rates of treatment success, especially in older patients," explained Jeffrey Lancet, MD, senior member of the Department of Malignant Hematology and chief of the Leukemia Section at Moffitt Cancer Center in Tampa, Florida.
AML is diagnosed in approximately 19,000 people in the United States each year and results in more than 10,000 deaths annually. Many patients with AML are older and have additional medical conditions, which makes treatment difficult. Only 50% of patients respond to existing therapies and the average survival time is less than 1 year. Therefore, researchers are trying to find new treatment options to increase survival.
Scientists know that cytarabine and daunorubicin work best in a particular concentration ratio. Unfortunately, the ratio is difficult to maintain in the body when the drugs are administered; therefore, they don't work as effectively as they could. CPX-351 is composed of lipids, which make up the outer membrane of cells and can form hollow spheres or vesicles that can be filled with drugs. Cytarabine and daunorubicin are present inside the CPX-351 lipid vesicle in a fixed ratio that is known to work most effectively.
This phase 2 study included 126 newly diagnosed AML patients from 18 cancer centers across the United States and Canada. The patients received the standard chemotherapeutic agents, cytarabine and daunorubicin, or the novel drug combination CPX-351.
"Patients with AML who received CPX-351 had a higher likelihood of remission than patients who received standard chemotherapy," said Lancet, who is the principal investigator and lead author of this study. The study was published in Blood (2014; doi:10.1182/blood-2013-12-540971). "In addition, CPX-351 led to longer survival in the large subset of patients whose AML arose out of a previously diagnosed hematologic disorder, such as myelodysplastic syndrome."
"The results from this study show a high degree of activity in AML, leading to the opening of the new, larger randomized phase 3 study, which will definitively determine whether CPX-351 is superior to standard chemotherapy," said Lancet.