So we are excited to say that yes we can do bone marrow biopsies but bone marrow biopsies are painful and we don’t do them as often. So can we use circulating tumor cells not only to count them because they are important prognostically but also to look at them by whole genome sequencing or by single cell RNA sequencing to really use them to identify patients who will progress or who will not progress, but to also understand the genomic features of those patients...
So we are excited to say that yes we can do bone marrow biopsies but bone marrow biopsies are painful and we don’t do them as often. So can we use circulating tumor cells not only to count them because they are important prognostically but also to look at them by whole genome sequencing or by single cell RNA sequencing to really use them to identify patients who will progress or who will not progress, but to also understand the genomic features of those patients. Because we know that numbers alone are not enough, we need to understand who’s truly high-risk and who’s not. And we can redefine smoldering myeloma by saying who is high-risk genomically, and we need to treat them in a different way than those who are not high-risk genomically.
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