That was a very interesting session because we’ve covered fields like acute myeloid leukemia, where we still have more questions than answers. But I thought that we got the problems presented, which is mainly how can we find an appropriate target without killing the normal myeloid cells.
For the acute lymphoblastic leukemias, we had talks on childhood ALL as well as on adult ALL...
That was a very interesting session because we’ve covered fields like acute myeloid leukemia, where we still have more questions than answers. But I thought that we got the problems presented, which is mainly how can we find an appropriate target without killing the normal myeloid cells.
For the acute lymphoblastic leukemias, we had talks on childhood ALL as well as on adult ALL. In childhood ALL I think the field is really advanced and we saw that particularly with the new trials and the real world evidence we can say that children really profit from CARs, maybe in conjunction with allogeneic transplant. For the adults, yes, we are also moving, but there are still problems related to how can we bridge patients either to CARs or to allotransplant and after CAR. So also here a bit more questions and more toxicity problems in part, but we’re moving.
In CLL, those were the first patients treated many years ago. We hear that they have still circulating CARs. So CLL is a real target. The problem there is that we are not always achieving complete responses. So it’s a very good treatment. But we have to think about ways on how to maintain the responses after CAR T-cells.
This transcript is AI-generated. While we strive for accuracy, please verify this copy with the video.