Ibrance and Fulvestrant stopped working. 😢oncologist wants me to do this trial. Has anybody had any experience with this trial or either drug?? Thanks for your help. Carla
giredestrant with Everolimus trial - SHARE Metastatic ...
giredestrant with Everolimus trial
I'm curious why your Onc would suggest a clinical trial so quickly? Have you been checked for the ESR1 mutation? You could be a candidate for the new Elascetrant. And you could try other Meds Verzenio, Kisqali with Faslodex or an AI? Maybe this clinical trial is very promising and about to end with very good results.
The thinking behind doing clinical trials is that the standard of care treatment will always be available for you while the trial may not be. If the trial drug is successful it will still take years for FDA approval. This is the philosophy at the cancer care center I go to for my primary care as well as the one for my second opinion. Of course, they are also both research centers so take that for what it is.
yes that is the reasoning behind getting on the trial. To be on this trial your first line of treatment has to have stopped working. This has to be your second line. It’s the only time I can do it. There are 2 arms to the trial. I could either get put on the standard of care arm or the trial drug arm. Who knows.
What would the standard of care be exactly?
examestane and Everolimus would be the standard of care arm.
I just looked up Girdestrant indeed it looks very promising but is still in clinical trials.
Be aware that different phases have different requirements and time commitments. Also a consideration is whether they have determined the dosage.
yes I have to ask more questions, especially about the dosage and the flexibility of the dose!! I assume not very flexible
Here is some info about the Giredestrant. I read somewhere else that it seems more promising for those whose hormones seem to be a real driver for their cancer to grow. onclive.com/view/giredestra...
Thanks for the info. I’m not going to lie switching meds is kinda freaking me out. Talking about it is helpful. Thank you.
Oh I know, it is scary! I’ve been through that twice now since being diagnosed with METS. Fortunately both times have ended up being ok but I fear I may have to switch sooner next time, so I’ll then be going through exactly what you are right now. I try to keep reassuring myself and have faith that all will be well. Some days are certainly easier then others but I do feel that keeping as positive a state as we can maintain, really helps us . I am struggling a bit with that at the moment though. This year has been a very challenging one for me so far, in a number of ways
I’m sorry it’s been a challenging time this year. Funny (not funny) how the regular struggles don’t stop. I totally agree with the positive attitude. I am grateful for lots of things but sometimes just get so scared. I gave myself a day to melt and will hopefully shut it down and keep on moving today. Might as well try and enjoy my 2 week med freedom!!! I hope you have a good one!!!