There are several open questions still, although we had progress. So the first open question is how to improve the results of treatments in higher risk MDS. We are stuck with the results of a study in a single drug that we studied that was already, I think, almost 20 years ago. So it’s an old study, but it was not possible until now to couple azacitidine with other drugs that are increasing not only the response, but also the overall survival of treated patients...
There are several open questions still, although we had progress. So the first open question is how to improve the results of treatments in higher risk MDS. We are stuck with the results of a study in a single drug that we studied that was already, I think, almost 20 years ago. So it’s an old study, but it was not possible until now to couple azacitidine with other drugs that are increasing not only the response, but also the overall survival of treated patients. So we are facing this big problem. It’s an obstacle. We are stuck with the results of 20 years ago. And although several clinical trials have been performed, none of them was successful in meeting the endpoints. So this is a very open question. The other increasingly important question is what to do with patients who do respond and then lose response to the first treatment line. So hypomethylating agents for high-risk MDS and for lower-risk MDS, the treatment with ESA’s and luspatercept and imetelstat and then lose response but still facing survival. So depending for some years on transfusions.
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