In a large collaboration with multicenter studies as well as AstraZeneca, we used the NeoGenomics database to look at patients with CLL who had had genetic testing sent and to see whether they had mutations in BTK when they were taking a BTK inhibitor. Of course, this is a very unselected patient population, but just interested to see when looking at very large numbers of patients who are presumably mostly still in remission, whether we see evidence of BTK mutations...
In a large collaboration with multicenter studies as well as AstraZeneca, we used the NeoGenomics database to look at patients with CLL who had had genetic testing sent and to see whether they had mutations in BTK when they were taking a BTK inhibitor. Of course, this is a very unselected patient population, but just interested to see when looking at very large numbers of patients who are presumably mostly still in remission, whether we see evidence of BTK mutations. We were able to see over 13,000, actually almost 14,000 patients. Primarily, these patients were on BTK inhibitors in the frontline setting. We did see a very low rate of BTK mutations at 1.7% in total. And we saw a few different types of BTK mutations with C41S being the most common. I think this is really exciting data because it tells us that we can leverage these large databases to understand better who is getting mutations and when people are getting mutations and we’re excited to take this further in the future to try to get more granularity on these data.
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