Denosumab

Hi everyone

after 6.5 years on my first line therapy of tamoxifen, zoladex and ibandronic acid for secondary bone Mets (diagnosed from the outset in 2016), at my review yesterday the consultant is concerned as I have become anaemic but they don’t know why. All iron, b-12 and folate levels are normal.

I was told it ‘may’ be the bone Mets starting to change after so many years on the same drugs.  So they want to change my oral ibandronic acid to an injection of Denosumab.

i am nervous of the change especially as it will involve visiting the hospital monthly to start with. 
Anyone else on this? How do you find it? Would love to hear some feedback. Thank you.

My friend is on denosumab long term and getting on fairly well.

Regular blood tests needed.
Subcut injections, not painful.

The only problem side effect she mentions from it are muscle aches…

Wishing you well :slightly_smiling_face:

I have been on it for nearly three years without any problem.  I am also on first line treatment - abemaciclib and fulvestrant.  For the first 18 months it was every four weeks but then it was reduced to 12 weeks. I go to the hospital for fulvestrant injections every four weeks and I have denosumab at the same time.  I don’t have any noticeable side effects from the denosumab and the injection doesn’t hurt at all. just the usual “sharp scratch”.  Good luck with it xx

I have been on denosumab for a while. Visit every four weeks to the hospital.

As people say it’s just a small injection in the arm (not like the horrid ones I used to have in my bucks).

My arm doesn’t hurt at all and it seems to be doing it’s job.

Good luck