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Expert Weighs in on Recent AML Advances

Angelica Welch
Published: Thursday, Sep 28, 2017

 Harry Erba, MD, PhD
Harry Erba, MD, PhD
Four major approvals this year have dramatically improved the treatment landscape for acute myeloid leukemia (AML).

In an interview with OncLive during the 2017 SOHO Annual Meeting, Harry Erba, MD, PhD, professor of medicine, director, University of Alabama (UAB) Hematologic Malignancy Program, UAB School of Medicine, reflected on these approvals and their effect on the treatment of AML moving forward.

OncLive: What have been the significant updates in AML over the past year?

Erba: For the clinician, the most important updates in AML are really the FDA approvals, because now we have to think about how we are going to incorporate these new drugs into our clinical practice. For decades, we have been using 3-and-7 daunorubicin-idarubicin with cytarabine as initial induction therapy for AML. 

What is the impact of the gemtuzumab ozogamizin approval?

Following the initial approval of gemtuzumab in 2000 based on relapsed/refractory patients with AML, there were a number of studies looking at the combination of gemtuzumab with chemotherapy in previously-untreated patients. There was a meta-analysis that combined gemtuzumab in various doses with induction and consolidation chemotherapy. Robert Hills published results from that meta-analysis which showed that there was a benefit in terms of overall survival, and event-free survival for CD33-positive AML patients who receive gemtuzumab ozogamizin during induction consolidation.

Then there is the MRC United Kingdom data showing that there was benefit, especially in younger patients who had core-binding factor AML, to adding a single dose of gemtuzumab ozogamizin, again 3mg/m2, on day 1 of induction.

Have you seen progress with FLT3 inhibitors? Are any distinguishing themselves?

  The first drug approved this summer for AML was midostaurin. Midostaurin has actually been around for a long time. It is a kinase inhibitor that is not very specific for FLT3 and actually inhibits a number of kinases, serine-threonine kinases, and tyrosine kinases, which have been implicated in AML. As you know, it was studied in FLT3 AML and when added to chemotherapy, showed an improvement in event-free survival and disease-free survival for younger patients.

However, there remains the question as to what is really the target for midostaurin in that population. Is it just FLT3 or could it be any of the other kinases that it inhibits? If you use a more specific FLT3 inhibitor, does it benefit patients with FLT3-mutated AML? We were hoping that we'd see marginal additional improvements on the outcomes that were seen with midostaurin by really targeting FLT3, but that is yet to be seen.

There are a number of drugs in development that are not yet approved for FLT3-mutated AML. The ones that are the furthest along would be gilteritinib (ASP2215), an inhibitor of both the FLT3 ITD and tyrosine kinase domain mutation; quizartinib (AC220), an inhibitor of the ITD; and crenolanib, a dual inhibitor of both ITD and TKD mutations. And there are others. As single agents, all of those drugs have shown biologic activity. Blast counts go down and you see differentiation of blasts. However, very few patients achieve complete remissions with restoration of blood counts. I think the future is going to be looking at the addition of those novel FLT3 inhibitors to induction and consolidation treatment. 

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