My husband (66) newly diagnosed with full blown CLL, otherwise good health. Just started on Imbruvica this week.. just trying to learn everything about the journey we are on. Waiting to get the results of the FISH test done a week ago.
I’m new here…: My husband (66) newly diagnosed... - CLL Support
I’m new here…
Welcome to you and your husband. He has started on a game changer medication for CLL, that has been so very successful, Imbruvica has resulted in a total of 3 BTK inhibitors that can be prescribed for CLL in the USA and a further 11 in clinical trials. We keep very useful posts in our Pinned Posts section here: healthunlocked.com/cllsuppo...
Start with this one healthunlocked.com/cllsuppo...
on 'brutinibs' to learn more about this medication and how later versions can be used if Imbruvica isn't well tolerated, etc.
Neil
Welcome! I am the partner of someone with CLL, and I think this is the best forum for finding out and sharing information. The administrators are excellent. Life in CLL research is moving so quickly, there is more hope now even than when my husband was diagnosed just 8 years ago.Beryl
How/why did he get a CLL diagnosis/start treatment without FISH? Since it takes 3 months of elevated cells with abnormalities for the diagnosis in the US, I am wondering why the FISH wasn't done sooner. I am only familiar with a FISH being done "before" treatment is started. Mine was done within the first month of elevated lymphocyte levels. Or are there other significant labs/findings that warranted immediate treatment? Or when you say "newly diagnosed", he has finished the 3 months of blood abnormalities/other testing & now the diagnosis is "official"? I am just curious.
Welcome to our group, I hope all the excellent "pinned posts" there are available answer a lot of your questions. And if not, please feel free to ask about anything & everything!
Immunophenotype flow cytometry testing is usually definitive for a CLL diagnosis, though sometimes the flow cytometry results can be confused, with close cousins to CLL. FISH testing is used for prognostic testing in the USA, but seldom done in other countries until just before treatment.
Thanks! I remember my doc saying "it takes 3 months to get a diagnosis" so am curious about the timeline.
Took me about half that 3 month period in Australia via our public health system. Most of that time was waiting time to see if my worsening neutropenia was due to an infection (giving it time to clear) or to eliminate blood testing errors. Acute leukaemias are diagnosed and treatment commenced much faster.
Mine was diagnosed with a blood test only the first time I saw a consultant 14 years ago now..
He never had a reason to see a doctor for years. In September he called a dr. friend and described weak legs, fatigue and enlarged abdomen.. we are a small town and he got him in for lab work and a ct with contrast within 2 days. His white count was over 207,000 and he was also anemic, and high lymphocytes.. his spleen is larger than his liver..we also saw the oncologist within a day after that.
He did have flow cytometry in the earlier lab work. And if you were staging it according to symptoms it would be a stage four I believe is what the doctor said.
Staging with CLL maybe a reference for doctors but is a poor reference in terms of symptoms, how the patient feels or treatment needs. You'll get used to all the "oddities" of this being chronic rather than acute and a blood cancer rather than a "solid" cancer. But we certainly understand this is very overwhelming at first and we empathize! We wish you the best of journeys!
Ahhh, that makes sense now. I agree super high white counts, anemia, fatigue/weakness, enlarged spleen.....all reasons to test urgently & the flow cytometry along with theses signs/symptoms would be reason to treat before the FISH results came back. And the cells likely had the classic CLL staining on the slides. Glad you have a good healthcare system that moved promptly!
And I would like to comment for those who have a lot of anxiety before/between tests....GrannyMyers' husbands' experience is a classic example of "if something might be urgent, docs jump on it. If his symptoms and results weren't a potential urgent problem, he wouldn't be asked to see an oncologist ASAP, or get the testing done ASAP. So those who have a lot of anxiety over something a doc says "hmm, here is something I want to monitor in case it turns out to need attention, let's check back in 3 months"... it really doesn't look like a huge problem to your doc. Otherwise you would be urged to be seen much much faster.
HI. Welcome to the family. Pleased to hear that he is on Ibrutinib, It has improved so many peoples life for the better. Best wishes.
Hi. Can you explain you mean by “full blown” ?
I wanted to ask that too😊 I thought CLL was a bit like pregnancy.. You either are or aren't 🤔
Full-blown? I imagine his enlarged abdomen and spleen might have felt a bit like being pregnant? 😊 Good to hear he's on Ibrutinib and on the list.
Well like I said new to this- first appt was Sept 20. Guess I just meant yes you definitely have a lot going on with everything blood levels,big sleep and liver ,etc. and yes I did tell him maybe he had an inkling of what pregnancy felt like. 😏
Welcome you and your husband to the group. My husband's 64 and he was diagnosed with CLL in November 2016 was on watch and wait for 9 months,and because he lost so much weight was put on ibruvinib, and been in remission just over 3 year's, and still on ibruvinib has chemo check up every 3 months,and speak's to his oncologist every 6 months.
This is an excellent forum. Another place to learn a lot is CLLSociety.org My husband has been on Imbruvica 7.5 years and doing great.
All the very best to you and your husband!!! I've said this many times, but I started on Imbruvica over 5 years ago and have not had any side effects even when starting treatment, and within 3 months my white blood count went from 650,000 (when I was hospitalized ) to NORMAL. My oncologist was amazed but was very happy about it as was I. I hope your husband has the same success as I have.