Well, everyone knows I’m sort of biased towards flow cytometry. I do believe that flow cytometry is a method that is available in many, many hospitals around the world. Nowadays, the implementation of EuroFlow NGF is very high, again across the globe. And I think that we can benefit from having one assay, two applications. So one assay, NGF, two applications, MRD assessment as in the past, in the marrow and nowadays also circulating tumor cells in the peripheral blood...
Well, everyone knows I’m sort of biased towards flow cytometry. I do believe that flow cytometry is a method that is available in many, many hospitals around the world. Nowadays, the implementation of EuroFlow NGF is very high, again across the globe. And I think that we can benefit from having one assay, two applications. So one assay, NGF, two applications, MRD assessment as in the past, in the marrow and nowadays also circulating tumor cells in the peripheral blood. And I’d like to say that regarding the assessment of CTCs in the blood, I think that for staging of a precursor condition or a newly diagnosed myeloma patient, NGF with its 10 to the minus 6 sensitivity is more than enough and data is showing a very strong prognostic value. And what we have recently published was the development of a new method that we called blood flow that achieves much higher sensitivity, 10 to the minus 7. It combines immunomagnetic enrichment and then NGF and this strategy may be even more powerful at the stage of treatment or post-treatment to really identify those patients at risk of relapse after achieving an optimal response.
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