Take anastrozole for the rest or your life?
My friend is 76. She has had BC twice…once in each breast. The last time was 4 years ago. Her oncologist told her she would have to take anastrozole for the rest of her life. Our cases are similar…different oncologists and I am 73…I was told I would finish after 5 years. Has anyone been told this or is currently taking it for the rest of their lives?
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I was just recently diagnosed last week with IDC and my first visit to surgeon Olay Moffitt in Tampa is August 7.
I am totally overwhelmed by all this and the waiting waiting waiting to be seen is insane.
@whr that was same situation for me. My oncologist (new since other retired) suggested onco test. Numbers very low. Estrogen level never checked before during or after. 🤷♀️. We must advocate for ourselves. Stay strong
@windyshores congratulations on your bone improvement. Tymlos seems to be working for you. That is wonderful you have improved that much to walk the 10 miles. Keep On Keeping On. 💪🏼
I totally agree, we need to ask questions and advocate for ourselves. Side effects are worse for me than for many others because I metabolize everything so slowly so the dosage needs to be adjusted, and results monitored. Your doctor has to be on board with "one size does not fit all", like clothing, lol.
I have another question? Are the people that are doing the BCI and Oncotype having genetic testing done before? I had the Oncotype test done after the second time I had BC. I was not aware of it the first time which was 2007. My score was low enough that I did not have to do chemo. After I had that test I had genetic testing done because it was a second time I had cancer. I have the CHEK2 genetic mutation. So my feeling is that neither one of those test could accurately predict anything for me. My assumption is that most of the people that are doing this testing have not had genetic testing done. So how does this work out in that case? So you think that you are doing something to relieve your anxiety and give you some peace of mind, and basically, I am wondering if we are not just a huge experiment.
Was wondering how f you know if feeling tired and fatigued BEFORE any treatment etc even starts is normal when first being diagnosed with IDC?
I’m so fatigued and I have not even been to Moffitt yet to start any treatment yet I’m just totally fatigued.
Wonderful news!
The question of these tests comes up a lot. Which I always find fascinating because when I was diagnosed they didn’t exist. My last most amazing doctor, and my current less amazing doctor never ordered any either. I have zero experience with them but wish I had the opportunity.
I did however have genetic testing done, not when I was diagnosed but much later, I have PTEN cowden syndrome. So pretty much breast cancer before 40 was in the cards.
I took tamoxifen for 5 years and anastrazole for 10, since I still have the hot flashes, I should have just stayed on it the rest of my life. Then again, bone destruction and horses probably isn’t a great plan.😂
Thank you one and all for sharing your stories, what tests you had and what decisions you made.
How many of you would stay on the drug to lessen you re-occurrence risk?
I’m on anastrozole. I’m not thrilled with the way it makes me feel and I will be on it for the next 9 1/2 years. My maternal grandmother, paternal grandfather, 2 uncles and an aunt all succumbed to their cancers. I will take my anastrozole until something better comes along. We all make choices that reflect our life experiences and I’m glad there is respect and acceptance for that.
If I had continued, I would have done 7 years, not 10, because I was told 7 was just about as good.
Want to clarify again that the Breast Cancer Index is only approved for use after 5 years of hormonal treatment and is only about risk of recurrence and benefit from doing more than 5 years. You can, like me, have high risk but no benefit. Or low risk and yes to benefit. Or low and no or high and yes.