Maybe the time is now for CTC assessment in myeloma, the assessment of circulating tumor cells. We have the methodology, particularly next-generation flow cytometry, to detect with very high sensitivity in a standardized way. This is a breakthrough that is possible in recent years. Now the detection and quantification is already important and prognostic and may be clinically relevant in all stages of disease – MGUS, smoldering myeloma, newly diagnosed active myeloma, and even during treatment, the assessment of peripheral residual disease based on CTCs...
Maybe the time is now for CTC assessment in myeloma, the assessment of circulating tumor cells. We have the methodology, particularly next-generation flow cytometry, to detect with very high sensitivity in a standardized way. This is a breakthrough that is possible in recent years. Now the detection and quantification is already important and prognostic and may be clinically relevant in all stages of disease – MGUS, smoldering myeloma, newly diagnosed active myeloma, and even during treatment, the assessment of peripheral residual disease based on CTCs. This is already extraordinary. Now, what if, beyond or in addition to detection and quantification, we could characterize the CTC clone from the genomic point of view. And this is where this abstract is providing the means, the tools that allow for genomic characterization of only a few CTCs with very robust methodology. So I think this will be a breakthrough in the field. Finally, not only detection, quantification, but also now genomic characterization of this clinically relevant subclone in the myeloma space.
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