I think it was quite a consensus, mostly on the fact that autologous stem cell transplantation is still a standard of care for most of us. We were mostly agreeing on this. And that the future is immunotherapy. Immunotherapy since the very beginning, so bispecific or CAR-T integrated with auto-transplant or substituting auto-transplant. So this was quite an agreement. Another agreement was on the MRD use...
I think it was quite a consensus, mostly on the fact that autologous stem cell transplantation is still a standard of care for most of us. We were mostly agreeing on this. And that the future is immunotherapy. Immunotherapy since the very beginning, so bispecific or CAR-T integrated with auto-transplant or substituting auto-transplant. So this was quite an agreement. Another agreement was on the MRD use. For sure newly diagnosed multiple myeloma is the setting where minimal residual disease is mostly useful to tailor treatment. Maybe a field of little disagreement was on how to tailor now on MRD because we do have some data but we do lack some other data so or not all the questions are answered so some of us were more keen to already use MRD to tailor maintenance duration some others were maybe hoping for additional data. So this is still something ongoing. And in the more elderly population, so newly diagnosed non-transplant eligible patients, currently we do have quadruplets and triplets. The integration of immunotherapy is ongoing. For sure the treatment duration is another still open question so on this there are still some controversies because initial data are not fixed duration treatments so it’s work in progress.
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