AML Induction Chemo Experiences?
 

Hi All!

Last night at midnight, I finished up my the last of seven units of cytarabine. During the first three days, I also had idarubicin. Though my diagnosis remains high-risk MDS (RAEB-2), this is the standard course of induction chemo for AML here at Duke

I know from research online that there's a well-established pattern of impact on blood counts, at least according the the FDA.

But I'd be interested in hearing from folks who have undergone induction therapy for AML and MDS about what your actual experience was with the drug in the period after administration: fatigue, infections, hair loss, whatever.

Please weigh in and let me know what to expect.

Thanks!

Greg

Greg,

I don't have any experience, but wanted to congratulate you on making it through the first steps! You will probably have some serious energy depletion when your WBC zeroes out. Not sure why this happens, but it is usually the low point with transplant as well.

You are in my thoughts daily, wishing you a strong and powerful recovery.

Dan

Thanks, Dan!

I really appreciate that.

Greg

Hi greg,
I'm new to this forum. 30 yr old from melb.. drs think I had mds that had already developed into aml when they discovered it. So with induction therapy I had the same drugs as you... I was extremely tired and had diarrhea and lack of appetite. Hair fell out after a couple of weeks (shaved it first.. too messy!) My counts were already shocking so had alot of transfusions! They didn't start to come up until about day 30. Unfortunately I discovered I'm allergic to a few anti nausea meds but I suggest you take them regularly. Good luck! Sorry you have to go through this. Lisa

Greg, My dad had induction chemo about 4 weeks ago due to a relapse from a haploid transplant. During his nadir, he received a donor lymphocyte infusion in the hopes of putting him remission and possibly a cure. At the moment he is in the hospital due to elevated temps and a suspected infection to his inner ear. Unlike you, he did a 5+2 with the same medications since they did not want to kill the graft that is there in the hopes the DLI with "clean up" the cancer cells.

He has hair thinning and minimal weakness. He tolerated the chemo really well but weeks later is suffering the consequences of low WBC, Plts, and Hgb. Due to his infection the plts have been taking a dive and he's been needing more transfusions. Let me know if you can anymore questions. He is also getting treatment at duke.

Chemo didnt work
 

Hello,

My 75yo father had MDS until 3 weeks ago when he was diagnosed with AML.
He started chemo with the 5+2 plan (instead of the 7+3). He had no side effects other than one high fever night and poor appetite, so things were going reasonably well, "according to plan" the doctor said...

Today, his marrow amalysis showed he still has 17%blasts, so doctor said that chemo didnt work for him... Now all his counts are low but he is feeling good...

I was really hoping he would be in remission, so this is really destroying me right now... Doctor said we have to wait till his counts go up a bit before talking about new options, though she doesnt seem very optimistic. She suggested Dacogen might be an option, but I havent find any promising info on that drug used in AML refractory to chemo...
Do any of you have any treatment advise? experiences?
THANK YOU SO MUCH for reading me, this is one of the worst days of my life (if not the worst)

Dacogen is very similar to the Vidaza that I was on after relapsing to AML. It worked great for me. After three cycles my blasts were less than 1 percent. It doesn't work for everyone but works very well for many. The side effects are usually minimal.

Thank you Bailie,

Im familiar with Vidaza but dont know much about Dacogen... reading about it in some web pages, it seems like vidaza might work better (and longer) than dacogen, dont know...

Any way, do you think having 17% blasts after first chemo cycle (5+2) is a good reason to stop it? (i was told when he started it, my father has over 80%).

I have been told about Clag and Flag ida as other treatments for refractory patients but never heard of them...

Hi Juan,

I am not an expert on Vidaza but have seen a number of presentations on it. A common theme is that the Vidaza must be continued a minimum number of cycles before it can be determined whether it is effective or not. Also, it is expected that counts will get worse before they get better. I can't remember offhand the minimum number of cycles (maybe 5 or 6?) but this article from 2014 talks about trying it for 6 months before stopping.

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3921030/

Just another data point for you to discuss with the doctor...

Best of luck!

We have learned that Greg Hankins, known in these forums as Greg H, passed away on July 24, 2016, from MDS and AML. His helpfulness, humor, willingness to share, and positive attitude were a model for all of us. We extend our condolences to his family.

Greg's blog

Obituary

This is very sad news, indeed. He will be missed.

So sad. He was an intelligent and kind man.

Greg's death is sad news. He was a wonderful friend to all of us on this forum. His posts were incredibly informative and helpful for me, especially when I was first diagnosed. He will be missed.

My sympathy to Greg's family.

Greg
 

I am shocked and saddened to read that Greg did not survive. May he Rest In Peace.