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Video

Real-World Evidence for Teclistamab in Myeloma | Dr. Rakesh Popat Shares #EHA2025 Insights

Posted by
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• June 19, 2025

Description

Discover the latest real-world data on Teclistamab for relapsed/refractory multiple myeloma, presented by Dr. Rakesh Popat at #EHA2025. Learn how this bispecific antibody therapy is performing outside of clinical trials, what it means for patient outcomes, and how it’s shaping the future of myeloma care.

On this video

Healthtree contact Rakesh Popat, Specialist

Rakesh Popat, Specialist

University College London Hospital

Transcript

Hi, my name is Rakesh Pabhat. I'm a hematologist and associate professor at University College London in the UK and I'm here at EHA 2025 and I'm presenting some real-world data with the use of teclistomab for patients with relapsed myeloma. So teclistomab is a bispecific antibody which targets BCMA, which is a target that we see on myeloma cells and it also hits a target on the immune cells, the T cells and it brings them together and in the clinical trials we found a response rate of about 60% and patients responded for about 11 months. But it's really important to find out how this drug works in real life patients and so what we did was that we teamed up across Europe and collected data for patients who were treated outside of clinical trials across eight European countries. So we looked at about 130 patients and what was important about this group of patients was that 60% of these patients wouldn't have been eligible for the clinical trial for various different reasons namely because their blood results might not have met the parameters but also they've already received one of these BCMA targeted treatments such as belantamab, aphrodotin or maybe a CAR T cell in the past and those patients couldn't have got on the clinical trial. Essentially what we found was that overall response rate was about 55% but if you remove the prior BCMA patients so the patients who'd already had the BCMA treatment it goes up to 65%. We found our patients respond on average for about 12 to 18 months and the durability of the response was over 20 months with patients living for over two years. So actually that data bodes very well compared to the clinical trial data because as I said at the beginning 60% of these guys patients would not have been eligible for the clinical trials to begin with. So it's really reassuring that when we're treating people in the real world at our cytokinical trials that we're getting quite strong results. Thank you.

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