This abstract is being presented by Kylie McLachlan on behalf of our group, which includes Dr Francesco Maura and Dr. Niels Weinhold and Dr. Usmani, as well as other co-authors. What we did in this study is sequence whole genome sequencing or whole exome sequencing or targeted sequencing of plasmacytomas, meaning tumors in either the bone or extramedullary. So, paramedullary or extramedullary plasmacytomas, as well as bone marrow sequencing...
This abstract is being presented by Kylie McLachlan on behalf of our group, which includes Dr Francesco Maura and Dr. Niels Weinhold and Dr. Usmani, as well as other co-authors. What we did in this study is sequence whole genome sequencing or whole exome sequencing or targeted sequencing of plasmacytomas, meaning tumors in either the bone or extramedullary. So, paramedullary or extramedullary plasmacytomas, as well as bone marrow sequencing. We compared genomic changes in the bone marrow to the plasmacytomas, and we see that there is increased copy number aberrations, increased mutational burden, and genomic complexity in the plasmacytomas compared to the bone marrow, suggesting that disease is arising from the copy number aberrations and may be more complex in its genomic characteristics. We present this data on about over almost 200 plasmacytomas samples and a large number of bone marrow samples as well.
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