Modern treatment paradigms in Acute Myeloid Leukemia (AML) are becoming more focused on individualizing treatment for each particular patient. There are different approaches and factors to consider in order to achieve this, which in turn carry various potential benefits. For example, high sensitivity tracking of AML residual disease is not only useful to ascertain the length of treatment, but it is also useful in determining the requirement for additional “maintenance therapy” after completion of standard treatment. C. Lai, et al, wrote an editorial reviewing precision medicine for AML. Their findings were first published as an Epub in Expert Review of Hematology in October 2015.
Here are the key benefits of this approach:
Targeting therapy to patient-specific somatic mutations
It is becoming widely accepted that identifying the location of mutations within the hierarchical clonal architecture of AML will be important to determine the most efficacious targets.
Ex-vivo veritas? Drug sensitivity and resistance testing
At present it is not always possible to effectively design individualized patient therapy against a particular target or pathway. Instead, investigators have employed high-throughput methods to screen a host of drugs for the ability to preferentially destroy ex-vivo AML cells from a specific patient compared with normal bone marrow. The advantage of this approach relies on the fact that treatment can then be selected as a result of preclinical evidence for a specific patient. In addition biomarkers can be identified.
High sensitivity measurements of residual disease burden and biology
Present AML response criteria are insufficient to stratify patients for risk of subsequent relapse and death. However, detailed sequential information regarding the amount of disease remaining to treat is equally as important as identifying the type of disease to be treated in any truly precision medicine strategy for AML. Also, the clonal composition of residual leukemia during or after treatment may provide predictive information in the form of biology, mutations or phenotype that are associated with response or treatment resistance to a therapy or combination therapy.
In summary, precision medicine for AML involves more than choosing the correct drug, or correctly characterizing the malignant clone. This paradigm is entrenched on the need to select the right treatment, for the right patient, at the right time – and repeating this process while monitoring for changes in disease burden and biology over time.
The goal of precision medicine is to personalize therapy based on individual patient variation, to correctly select the right treatment, for the right patient, at the right time. Acute myeloid leukemia (AML) is a heterogeneous collection of myeloid malignancies with diverse genetic etiology and the potential for intra-patient clonal evolution over time. We discuss here how the precision medicine paradigm might be applied to the care of AML patients by focusing on the potential roles of targeting therapy by patient-specific somatic mutations and aberrant pathways, ex-vivo drug sensitivity and resistance testing, high sensitivity measurements of residual disease burden and biology along with potential clinical trial and regulatory constraints.