HI Debs
I am at the Royal Marsden in Sutton. Not sure what the study is called as I am just at the pre screening stage but I think it is for a drug called Tucatinib. Don't really know much about the study as I was already a bit overwhelmed when they suggested it as I had just heard my mets had spread. As it just involved a blood test at this stage I did not feel like I needed to know much more. Still don't understand how my HER2 status could change but just have to see. If it offers me more treatments, so much the better.
Although I did say on JUST involved blood tests, it did take they 2 hours to find a vein!!
Good luck with your treatment.
Sarah x
Hi Sarah,
This sounds interesting can I ask the name of the trial and the hospital running it please.
I too have liver and bone mets HER neg
Thank you
Debs x
That sounds really interesting Sarah , I hope it gives you and others some more options for treatment .You could also ask about this in the Ask the Nurses section and you can request a call back from the nurses to discuss also . Good luck with your treatment . Jill x
HI
when I had my original primary I was told I was HER2 neg. Now several years down the line with liver and bone mets, I have been offered the chance to take part in a trial. Apparently even if you biopsy was HER2 neg I could still have some HER2. They have done a blood test to confirm and if it finds HER2 I can take part with drugs for HER2 pos tumors.
Sorry if I have not explained it well but i don't fully understand it.
Just wondered if anyone had been told anything similar. Go back in 3 weeks to get result and see next line of treatment.
Thanks
Sarah