Hello All,
Three months ago, my 19 year old son was diagnosed with CML in the chronic stage. Of all the sources of information I've found, this support group has provided me with the most comfort and clearest information. I'm hoping you can provide a nervous mom with some insight.
After diagnosis, my son was started on Hydrea until we were able to meet with his oncologist a couple of weeks later. At that time, he was put on 100mg of Dasatinib. Due to a liver enzyme increase, (Alkaline phosphatase ALP) he stopped taking the Dasatinib about 3 weeks ago to see if that would bring the enzyme down. It has been decreasing slowly, but remains quite high. He is now scheduled for an ultrasound to check his liver, and he will be switching medications in the next week, though we don't know which one he will be put on yet. His last blood work showed his platelets and hemoglobin now squarely in the normal range, and his WBC has risen slightly to 12 after being in the normal range for the previous 3-4 weeks. He had a BCR ABL test done last week, but we won't know the results until we meet again with his oncologist in early August.
How nervous should I be about this development? I know that we are in very early days, and I have seen a number of people comment about spikes in liver enzymes early on. However, I've not seen much talk about ALP specifically.
We've been told that our son's prognosis is good, and the logical side of my brain knows that this is still very early in the process, there are multiple drugs to try, and that the next 12-18 months is about finding what works for him. The emotional side of my brain is admittedly trying really hard not to freak out. As a parent, the emotional rollercoaster is excruciating.
Any insight would be greatly appreciated.
Thank you.