The first thing is to define or discover novel markers which affect post-transplant outcome. APOE and APOE germline variation is a vivid example of this. And second, I think a major challenge in transplantation is the outcome of HLA mismatched patients and patients not having a fully matched donor. We need to improve their outcome, we need to reduce non-relapse deaths...
The first thing is to define or discover novel markers which affect post-transplant outcome. APOE and APOE germline variation is a vivid example of this. And second, I think a major challenge in transplantation is the outcome of HLA mismatched patients and patients not having a fully matched donor. We need to improve their outcome, we need to reduce non-relapse deaths. And this is a major obstacle in transplantation still. Another interesting question is how do we deal with patients who were refractory to primary treatment and how do we act? Do we aim to reduce leukemic burden in order to improve outcomes or is it just improving non-relapse mortality and toxicity of the transplantation? We don’t know that exactly, but there is emerging data helping us to make the best judgments and decisions.
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