We had the opportunity to share what we are doing in Italy with real-world data and registries. So mainly we have in Italy a myeloma registry which is actively enrolling up to 1,900 patients. So the goal of course is to collect all demographic clinical data to be able to have a real look on the outcome of patients, different treatments among the countries, what is related to quality of life and so on...
We had the opportunity to share what we are doing in Italy with real-world data and registries. So mainly we have in Italy a myeloma registry which is actively enrolling up to 1,900 patients. So the goal of course is to collect all demographic clinical data to be able to have a real look on the outcome of patients, different treatments among the countries, what is related to quality of life and so on. The second project that we discussed is the biobanking project that’s not only Italian, it’s Italy plus the Netherlands plus other European countries. We have the opportunity to have this study aimed at the biobanking 5,000 patients. So biobanking, what does it mean? Both bone marrow, peripheral blood and eventually extramedullary sites of the disease. So with the aim of putting those samples available for whatever project it will come, so maybe to look at MRD negativity in those patients in real life that don’t have a baseline sample, look at specific subset population, extramedullary disease, plasma cell leukemia and so on. So I think that’s a huge treasure, so it’s a very ambitious project.
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