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CAR-T Meeting 2024 | Selecting patients with myeloma for CAR-T: important clinical considerations

In this video, Rakesh Popat, BSc, MBBS, MRCP, FRCPath, PhD, University College London Hospitals, London, UK, briefly discusses how to appropriately select patients with multiple myeloma for CAR-T therapy. Although patients with aggressive disease tend to have poor outcomes with CAR-T cells, bridging therapy may be provided in this setting. Other important factors to consider are level of disease burden and presence of extramedullary disease (EMD). This interview took place at the EBMT-EHA 6th European CAR T-cell Meeting in Valencia, Spain.

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Transcript (edited for clarity)

Multiple myeloma now has two licensed CAR T-cell products, so we’re trying to ascertain the best patients which we should be using. One of the things which is becoming apparent, or the patients not to use, are the patients with aggressive, widespread relapse because essentially the outcome of those patients is poor and we also see lots of CRS and ICANS.

So really what we’re trying to do is to select your patients, or if you do have a patient in that setting is to give adequate bridging therapy...

Multiple myeloma now has two licensed CAR T-cell products, so we’re trying to ascertain the best patients which we should be using. One of the things which is becoming apparent, or the patients not to use, are the patients with aggressive, widespread relapse because essentially the outcome of those patients is poor and we also see lots of CRS and ICANS.

So really what we’re trying to do is to select your patients, or if you do have a patient in that setting is to give adequate bridging therapy. What we know with cilta-cel is that the risks of getting the late neurotoxicity that we see is associated with significant disease burden and high CAR-T expansion and CRS, and we have to manage that very rapidly.

So back to the original question, we have to select those patients more appropriately as having a lower disease burden or if we can’t do that, we’d have to give adequate bridging therapy for that.

The second problem is that we are seeing that we are unable to give the CAR T-cell product due to worsening disease in the manufacturing process. So again, what we’re looking for is patients with a slightly lower disease burden, a slightly lower disease tempo and lower extramedullary disease. These are the patients who are going to do much better with CAR T-cell therapy.

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Disclosures

Consultancy: GSK
Honoraria: GSK, Janssen, BMS, AbbVie, Roche
Research Funding: GSK
Current Employment: University College London Hospitals NHS Foundation Trust.