So what I see is a more integrated approach of all kinds of different markers that we can use. Not only genetic markers, but maybe also proteomic profiles that we see more often. So to refine all the information… to refine the diagnosis and prognosis by having all the information together. So that’s on the one hand.
I think on the other end of the spectrum where we aim for more sensitive monitoring, I think what our main challenge is also is to see whether if we use the circulating cells in the blood, if that’s enough for monitoring the remissions or whether we need other materials or in fact other technologies to try and access information from other compartments in the body...
So what I see is a more integrated approach of all kinds of different markers that we can use. Not only genetic markers, but maybe also proteomic profiles that we see more often. So to refine all the information… to refine the diagnosis and prognosis by having all the information together. So that’s on the one hand.
I think on the other end of the spectrum where we aim for more sensitive monitoring, I think what our main challenge is also is to see whether if we use the circulating cells in the blood, if that’s enough for monitoring the remissions or whether we need other materials or in fact other technologies to try and access information from other compartments in the body. So I think especially the cell-free liquid biopsy analyses are going to be very interesting to see how those can contribute to that further monitoring.
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