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SOHO 2023 | The current SOC in AL amyloidosis: dara-CyBorD & considerations for patients with relapsed disease

In this video, Angela Dispenzieri, MD, Mayo Clinic, Rochester, MN, talks on the use of dara-CyBorD as a standard of care (SOC) for patients with light chain (AL) amyloidosis, plus or minus a stem cell transplant (SCT). Dr Dispenzieri discusses the requirement for additional studies to refine this treatment regimen and improve complete response (CR) rates, and concludes by addressing considerations for patients with relapsed disease. This interview took place at the Eleventh Annual Meeting of the Society of Hematologic Oncology (SOHO 2023) held in Houston, TX.

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Transcript (edited for clarity)

AL amyloidosis, now, of course we have daratumumab, cyclophosphamide, bortezomib, and dexamethasone as the standard. It’s wonderful to have a regimen as effective as that one. There’s much we need to do in that space because, although you have CR rates of 50% or better, it’s not everybody. We also don’t know how long these responses are going to last, so we need additional follow up...

AL amyloidosis, now, of course we have daratumumab, cyclophosphamide, bortezomib, and dexamethasone as the standard. It’s wonderful to have a regimen as effective as that one. There’s much we need to do in that space because, although you have CR rates of 50% or better, it’s not everybody. We also don’t know how long these responses are going to last, so we need additional follow up. We need to know if there are other drugs to add or if you need all the drugs in that regimen. Will the two-year kind of maintenance period or full therapy be sufficient? So there are a lot of questions even with that regimen. But I think it’s very exciting to have something showing such good results. It clouds what we do with stem cell transplant as first line- but that is pretty much the standard these days, is that as an induction plus or minus transplant, but there is less and less stem cell transplant in that space. And then, relapsed disease is a little bit the wild West, borrowing from what we know from small Phase II trials and also what we know from multiple myeloma. But being cognizant of the toxicity being a little higher in AL patients than it would be in multiple myeloma patients.

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