← Return to I am newly diagnosed with AML. with the inv(3) mutation,

Discussion
Comment receiving replies
Profile picture for edelgado13 @edelgado13

My brother was diagnosed with AML MECOM inversion 3 and now they believe it came from undiagnosed MDS he is 38. They have gone back 2 years and by looking at labwork they think he had MDS years prior, He is at MD Anderson underwent targeted therapy and BMT transplant at day 72 his bopsy showed cancer 5% blast now we are at day appro 120 after BMT and he is having to return to MD Anderson they believe the cancer is back and more aggressive can someone with this mutuation please tell me what treatment they have done and how many years out they are?

Jump to this post


Replies to "My brother was diagnosed with AML MECOM inversion 3 and now they believe it came from..."

Hi @edelgado13 Oh gosh, I so sorry to hear about your brother’s setback after all he’s gone through already with his AML and BMT. AML can be a formidable. Some of the mutations and subtypes with genetic abnormalities can sure keep our doctors on their toes. Your brother is in excellent hands with MD Anderson. They have the deep bench of knowledgeable hematology oncology specialists to hopefully be able to offer some innovated treatment options for him.
At 38 he’s so young to be going through all of this. But his age can also work with him. I’m sure he, along with all of you, his family and friends, are so disappointed and frustrated. But there is more to be done and I’ll join you in hoping for the best! I had AML with several aggressive mutations, 7 years ago and learned to never give up hope!

Because MECOM Inversion 3 is a rare bird it may take time for others to see this post and pop into the conversation. But I’d really like to follow along with your brother’s journey. I’m here if you need a shoulder or sounding board.
Will you keep me updated on his treatment please?