Video

Potential Role of Syk Inhibitors in ITP

Transcript:

Ivy Altomare, MD: What about new agents? What do we have coming down the road? I would imagine that new agents are probably most often being tested in the refractory setting? I’d like to start with fostamatinib.

Terry Gernsheimer, MD: That’s an interesting drug. It’s a Syk inhibitor.

Ivy Altomare, MD: What’s a Syk inhibitor?

Terry Gernsheimer, MD: I’m not an immunologist, so I don’t want to start getting into that. But, basically, we’re changing the immunology of recognizing these cells, or platelets, as targets.

Ivy Altomare, MD: OK. Syk standards for spleen tyrosine kinase, I believe?

Terry Gernsheimer, MD: Yes.

Ivy Altomare, MD: I haven’t heard of another Syk inhibitor available. Is that the first-in-class?

Terry Gernsheimer, MD: As far as I know, it’s the first-in-class. The original data, which looked at the usual endpoint (which is 50,000, at least doubling of the platelet count in patients who were at less than 30,000 to start), didn’t look great. It was about 18% on response rate. If we look at the data, if we look at a secondary analysis, what are we really looking for in patients? We’re really looking for clinical safety, right? We’re not necessarily looking for that 50,000 target because, frankly, other than the TPO mimetics, I’m not looking for that 50,000. I’m usually looking for greater than 20,000 or 30,000, because that’s usually what will keep patients safe. And, that’s what the guidelines say. If you look at the secondary analysis with fostamatinib, what you find is that they looked at, let’s say, 30,000, or at least a 20,000 increase. And when you look at that, we’re talking more like 40%, 45%. So, it’s promising. I think we need some more long-term data, which I think they’re in the process of obtaining.

Ivy Altomare, MD: Yes.

Terry Gernsheimer, MD: But, it is definitely somewhat promising. So, I’m excited about it.

Ivy Altomare, MD: A response rate of 40-ish percent in refractory...

Terry Gernsheimer, MD: That’s the clinically significant response rate, as opposed to the usual response rate that we’re looking for, which is greater than 50,000.

Ivy Altomare, MD: And this drug is oral?

Terry Gernsheimer, MD: It’s an oral drug.

Ivy Altomare, MD: OK. So, it’s oral, continuous?

Terry Gernsheimer, MD: Yes. You have to take it daily. You lose the response if you stop the drug.

Ivy Altomare, MD: What’s known about the tolerability?

Terry Gernsheimer, MD: Actually, it’s been relatively well tolerated. Initially, we thought that we were seeing a lot of gastrointestinal side effects at higher doses, but it seems to be much better tolerated now. I was looking at the data yesterday and I’m actually pretty impressed that it is a tolerable drug. It will have a place, along with a lot of other drugs that are coming down the pike that are looking at immunosuppression in other ways.

Transcript Edited for Clarity

Related Videos
Craig Eckfeldt, MD, PhD, assistant professor, medicine, faculty, Microbiology, Immunology, and Cancer Biology PhD Graduate Program, Division of Hematology, Oncology, and Transplantation, the University of Minnesota Medical School
Mark Juckett, MD, professor, medicine, Division of Hematology, Oncology, and Transplantation, the University of Minnesota Medical School
Timothy Hughes, MD, MBBS, FRACP, FRCPA
Hannah Choe, MD, an expert on GVHD
Hannah Choe, MD, an expert on GVHD
Grzegorz S. Nowakowski, MD
Combination of Zanubrutinib + Venetoclax for Treatment-naive CLL/SLL With del(17p) and/or TP53: Preliminary Results From SEQUOIA Arm D
Preliminary Efficacy and Safety of the Bruton Tyrosine Kinase Degrader BGB-16673 in Patients With Relapsed or Refractory CLL/SLL: Results From the Phase 1 BGB-16673-101 Study
Results from the randomized phase 3 DREAMM-8 study of belantamab mafodotin plus pomalidomide and dexamethasone (BPd) vs pomalidomide plus bortezomib and dexamethasone (PVd) in relapsed/refractory multiple myeloma (RRMM)
Hannah Choe, MD, an expert on GVHD