I’ve just finished my tenth year since my Stage IV diagnosis of CLL and my questions today are about the incidence of gout in patients who have been in various forms of treatment. Early on, my Uric Acid was only an issue in case that tumor lysis syndrome was an outcome of the treatment. Later on, TLS became a more everyday issue especially during my time on Ibrutinib or Acalabrutinib when I think it became a much more acute problem. I went for about 4 years without a Uric Acid test during which time I think I started developing gout issues which really became a serious problem during IBTN, it got so bad that I had to have surgery to remove a tofacious gout nodule from the middle of my right foot which was also packed with CLL cells.
When it was clear I was going to have to have surgery, they needed my Platelets at 50 or above which was a problem because of my history with ITP, as a they had been running in single digits to teens. I had a 5 course treatment of IVIG which got the Platelets up high enough, but it also triggered a very serious case of TLS. So I got the Platelets up, had surgery and within a week was back in the hospital with a HgB of 5 because so many red blood cells had died with a very serious case of hemolytic anemia. It was my greatest brush with death in the prior 8 1/2 years. I ended up having to have a complete blood transfusion and after which I started on Venetoclax, which began with 6 monthly treatments of Rituxan as well as bi monthly treatments of IVIG and now 19 months into it, I have blood test results of a normal human being, with one exception, Uric Acid, which is causing recurring gout problems in my feet mostly.
I’ve tried to treat with high dose allopurinol, 400 mg a day, and I only lasted a few weeks on it and had to take it back to 100 mg a day and ultimately had to stop it, so I started Uloric at 40 mg and I lasted but 10 days on that drug before all hell broke loose in a variety of ways, but luckily I didn’t have any cardiac problems like I did while on Ibrutinib.
So, I’ve decided that with 5 months left on Venetoclax, I am going to roll the dice with the Uric Acid reducer drugs hoping that when I stop Venetoclax the cell death problem will moderate and won’t be so much of an issue. 100 mg of allopurinol a day seems to keep my Uric Acid at just about 7, but I can’t get to 5 without a lot more. In the end, its just easier to deal with the gout flare than it is to try to fix the uric acid issue, for me at least. This is a thesis I am working on with my Oncologist and Rheumatologists at Dana Farber.
So, to get to my question, what is everyone’s experience with increased uric acid levels while on later stage treatments for CLL, have you had to be on ongoing Allopurinol or alternatives, has it caused you to have gout and if so, how serious has it been, i.e. how odd has my need to have surgery done. Sorry for the length of this post but its surely been a tough journey during which gout has become one of the most serious outcomes and surely greatest cause of concern!
Thanks in advance for offering your thoughts.