If you have access to CD123 targeted therapy, you must use targeted therapy. If you do not have access to these new molecules, one way is to use chemotherapy, as we have demonstrated in our study. But this treatment is efficient if the patient could support it, because in our study, two-thirds of the patients cannot receive all the treatment. If the patient can receive the treatment, there are some good results with 80% of remission, but at a global level, only 40% of the patients finally survive...
If you have access to CD123 targeted therapy, you must use targeted therapy. If you do not have access to these new molecules, one way is to use chemotherapy, as we have demonstrated in our study. But this treatment is efficient if the patient could support it, because in our study, two-thirds of the patients cannot receive all the treatment. If the patient can receive the treatment, there are some good results with 80% of remission, but at a global level, only 40% of the patients finally survive. We have also tested a new combination of new molecules, but that are not approved for use in the treatment of this disease. It’s the association with proteasome inhibitors, BCL2 inhibitors, some new combinations and we have published last year a small study with very promising results. And so in France now where there are new cases, we recommend using this unapproved molecule because it’s safe, it’s efficient and it’s non-toxic.
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