Very sorry to hear of your friend as AML is a terrible disease. The good news is there has been a lot of progress made with treating AML in recent times, especially around less intense treatment protocols that use venetoclax. It is really impossible to provide advise other than to suggest that your friend consult widely with different haematologists about the best treatment options for them as there will be differences of opinion between the different doctors.
Bisantrene is experimental and potentially only suitable for your friend if he/she has failed all conventional treatment options. I know a number of patients from Europe have accessed bisantrene via the ongoing Sheba trial in Israel, but your friend doesn't need to worry about this right now.
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