Hello all,
After a struggle to get on top of my CML due to Imatinib failure, then extremely suppressed blood counts on Nilotinib things looked to finally be getting a bit better. I had my first BM biopsy on the request of a new consultant and my BCR/ABL had finally reduced to 1% with low but acceptable blood counts.
Then I was hit by the bad news that not only do I have the Philadelphia chromosome (9:22) but I also have another chromosome clonal abnormality known as Monosomy 7. Out of ten cells cultivated, two were PH+, three were normal and five had this new issue with chromosome 7. This is potentially very serious and could well lead to MDS and AML. On the face of it, it seems as though they are two separate issues although I don’t believe that can be the case. There’s just too much coincidence for that. Does anyone else have experience, or have you heard about, anything to do with this in conjunction with CML? I’ve been told it’s 50/50 to whether the 7 abnormality progresses further and if it does the only option is a stem cell transplant. I’ve already met the transplant team and my sister is being tested to see if she’s a match. The odds don’t look good if it progresses so any info is welcome. Oh, and the only way of monitoring the situation is regular BMB’s 😩
Thank you in advance.