Bill's Friends and Family

Friday, March 7, 2008

March 7th- ABT-869

For all our medical friends and family, here is the scoop on the clinical study in layman terms. I hope others, who want to know, will also understand this explanation.
Abbott Laboratories has a chemotherapy drug that has been successful in controlling the cancerous growth of some tumors because it blocks the growth of new blood vessels and kills cancer cells. It is now being tried on Leukemia patients, like Bill, who have a chromosome mutation called FLT-3 Positive. This is the mutation that is very aggressive, and other chemotherapy treatments have not been able to control it (as we well know). Bill is the third person at The University of Chicago Hospital to be involved with this study. The other patients are 2 and 3 weeks ahead of him. It is too soon to tell if the drug is successful, but the other patients are far enough ahead to know what side effects need to be addressed.
Bill will take 10 mg of this drug in liquid form, mixed into Ensure for 26 days. The first day (Thursday) he had a blood draw every 15 minutes for the first hour. Then every half hour, then hourly for the rest of the day. The laboratory wants to monitor the drug in his blood stream, and watch how his body is handling the drug. This drug is experimental and is not approved by the FDA. It has the same side effects as other chemotheraphy drugs. After the first day, Bill is doing fine.
Bill will have his second dose Friday night, and future doses will be in the evening with blood work being drawn twice daily.
I have learned that Bill will not come home unless his good white cells improve to the point he is no longer neutropenic. Just like we watched the cancerous white cells decrease this week, we will want the Neutrophils (good white cells) to improve next week. Blasts in his blood stream are down to 14%.
Bill was even better today. He has an appetite, we took three walks (together), and he asked that I bring his book to read. Bill has not wanted to read since December. (I guess it takes red cells, oxygen to the brain, to read). He is conversational again and I feel like “our Bill” is back.
I have begun to realize that you are all on this roller coaster ride with us. When I didn’t get a blog off for a few days this week, my phone was ringing. I don’t like to make entries when there is a problem, until the crisis is over. And sometimes there is a “crisis” everyday. But the past 2 days have shown improvement everyday.
Let us pray for Bill’s continued improvement and God’s work in helping new drugs be developed to fight disease. Amen

7 comments:

Anonymous said...

We are thrilled that the first day of the experimental drug went well, and with all of our prayers may the days to come be just as successful.

We will continue to pray and think of you often. Maybe for a few days the roller coaster won't be so bumpy. Keep walking.

Love,
Paula and Jim

Anonymous said...

I hope everything continues to go well. Knock wood! Nancy, thanks for keeping us so well informed.

Thinking of you,
Janet and John

Love the pics of Maggie and Andrew!!!

Anonymous said...

So glad things are moving in a positive direction. New and improved is always better, and we all become stronger when we travel into the unknown! I can just picture you two walking hand in hand - and leaving bread crumbs along the way.

I am one of those "obsessed" with the blog, as you well know. Your postings help all of us who crave for information.

Thanks for taking the time to keep us informed - and for taking care of Bill. Just remember to take care of you too!

Love, prayers, and good health,
Gail

Anonymous said...

Howdy Hubers!

It was so good to see Bill the other day, and I'm glad to see that things are still getting better. Michelle and I wish the best for both of you during this trial.

It takes a lot of courage to venture into new territory, but that's how we discover great things in this world. We continue to pray for health and recovery along this new path.

God bless,
Justin and Michelle

Anonymous said...

That is such wonderful news.. It was a blessing to see both of you on Wed. Bill was far better that day than I could have ever hoped for. Let's hope this works. I just love the new baby pictures. They are just so cute. As always our love and prayers.
Pat

Mickey Hornack said...

Good to hear positive things. Think of you folks alot. Hoping for very successful therapy and an improving forecast on a regular basis.

Anonymous said...

Praise God that the new drug seems to be going in the right direction.
You both, as well as your families, have been in our prayers from the start. Even Cory and Dune ask God in their nightly prayers to 'help Mr. Huber to get better'. They have witnessed the power of prayer 2 times in the past 2 months with their own family members' illnesses, and so at a tender age have learned to believe in God's awesome power.

Thank you for keeping up the blog; we turn to it often as we think of the trial you both are going through.

Our prayers will always be with you.

Ken and Jeri