Today, as you know, the TP53 mutated MDS are very poor, very poor outcome. So today we continue to treat this patient with azacitidine and if by chance, if we obtain a response and if the patient is eligible to allow stem cell transplantation, we try to transplant this patient. We discuss also to use after transplant a maintenance treatment using azacitidine or azacitidine plus DLI in prophylactics as prophylactic treatment because we know this patient relapse...
Today, as you know, the TP53 mutated MDS are very poor, very poor outcome. So today we continue to treat this patient with azacitidine and if by chance, if we obtain a response and if the patient is eligible to allow stem cell transplantation, we try to transplant this patient. We discuss also to use after transplant a maintenance treatment using azacitidine or azacitidine plus DLI in prophylactics as prophylactic treatment because we know this patient relapse. So this is the standard of care for today for this patient. But unfortunately, if there is no transplant, the median overall survival of the patient stays around six to nine months. So we try to design some clinical trials to improve the outcome of this patient. And with the French group of myelodysplasia we designed some clinical trials and we hope to open some clinical trials very soon in first line but also in second line in a relapsed/refractory setting and we hope maybe to improve the outcome of this patient.
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