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VJHemOnc Podcast

Advances in CAR-T and cellular therapy from EBMT 2020: MSCs, clinical trial updates and gene-edited effector cells

Oct 1, 2020
Experts discuss recent updates in CAR-T and cellular therapy, including T cell engineering, CRISPR gene disruption, mesenchymal stem cells for COVID-19 pneumonia, and CAR-T cell therapy in challenging patient populations. They also analyze studies on CAR-T cell therapy, comparing management of toxicities, eligibility criteria, and durable responses. Additionally, they explore a comparison study between exocaptogen, CIBMTR, and T-stinlucil, and the potential of gene-edited effector cell therapy.
20:15

Podcast summary created with Snipd AI

Quick takeaways

  • Advancements in CAR-T and cellular therapy include the use of mesenchymal stem cells for graft versus host disease and potential application in COVID-19 inflammatory disease.
  • Gene-edited effector cell therapy offers the potential to improve T-cell therapies by enhancing potency and creating off-the-shelf T-cells without graft-versus-host disease risk.

Deep dives

Advancements in Cellular Therapy for Hematological Malignancies

The podcast episode explores recent updates in CAR-T and cellular therapy for hematological malignancies. The first discussion focuses on the engineering of T cells and the use of mesenchymal stem cells for treating graft versus host disease (GVHD). The efficacy of CAR-T cell therapy and the use of CRISPR to disrupt genes are highlighted. Additionally, the potential application of mesenchymal stem cells in COVID-19 inflammatory disease is discussed. The second part of the podcast delves into CAR-T cell therapy for multiple myeloma, highlighting studies such as Karma, Cartitude 1, and Evolve that demonstrate high response rates and durable remission durations in a refractory patient population. Lastly, the podcast covers key clinical trials involving CAR-T cell therapy for refractory-diffuse large B-cell lymphoma, including Zuma1, Juliet, and Transcend studies, which show comparable durable responses and acceptable toxicity profiles.

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