What is your approach to the decision to use CPX-351 or standard 7+3 for de novo AML?
Do you await molecular and cytogenetic results prior to initiating therapy, or does age and function status primarily drive your choice?
Answer from: Medical Oncologist at Academic Institution
CPX-351 is a dual-drug liposomal encapsulation of cytarabine and daunorubicin that delivers a synergistic 5:1 drug ratio into leukemia cells to a greater extent than normal bone marrow cells. It was approved by the FDA in 2017 for the treatment of adults with newly-diagnosed therapy-related acute my...
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Medical Oncologist at Texas Oncology What are you doing to temporize while awaiting mol...
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