Anastrozole - should I take?
I'm 73, and was recently diagnosed with stage ER/PR+, HER-2- Invasive ductal carcinoma, grade 1a, of the R Breast and had a lumpectomy. I have a 13 Oncotype DX score and negative for the BRCA1 and BRCA2 genes after doing genetic testing. In 1994, I had stage 1 breast cancer of the L Breast and had chemo and radiation. Then, in 2001, I had a complete hysterectomy (including ovaries) after being diagnosed with stage 1 uterine cancer. The radiation in 1994 caused me to develop a left bundle branch block of the heart. I haven't made a decision whether to take the suggested Anastrozole. I'm considering alternative treatments rather than take Anastrozole because I've heard horror stories about its side effects. I already have macular degeneration, and the left bundle branch block. If you have a similar story, or refused the AI inhibitors because of side effects, could you share it with me?
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Gee, thank you!
I declined AIs since I have osteoporosis and my cholesterol tends to be on the high side, and AIs worsen these conditions. I take Tamoxifen, which generally isn’t offered to post menopausal women - AIs are the drug of choice.
I asked my oncologist about the difference in effectiveness between AI & Tam for my specific situation - Oncotype of 0, tumor stage 1, grade 1, no lymph involvement. She said that in my case, while AIs would maybe be a tiny bit more effective to prevent recurrence, but given my other conditions, Tamoxifen makes sense.
I don’t believe she would have offered me Tamoxifen if I hadn’t asked - I think they are trained to only offer the guideline directed therapy, unless the patient asks. I was surprised at the reaction from my other doctors (surgeon, radiologist, primary care) that I’m taking Tamoxifen & not an AI, they seem to assume that AIs are the only option for post menopausal patients.
I think it’s important to discuss concerns with your doctor, try the meds if they make sense, and know that if you develop issues, talk to your doctor so they can stop or change them.
Why are they recommending you have your ovaries removed?
Thank you!
My surgeon said that ovaries are connected to somehow breast cancer. They have seen it spread there to ovaries.
He also suggested redoing my breast implants. My breast implants were done around 1995 Mayo Clinic by Head Surgeon Dr Paul Schnur. They seem to be holding up pretty good so far, but he said like old tires 🛞 gradually deflate. Ugh 😩
What is you cancer type? Did you do MamnaPrint? When diagnosed? What do you take? Age?
Thanks for reaching out.
Jane W.
Very helpful your share to know if taking Lexitrole disturbs me and causes conditions. I hate all pills 💊. Ugh.
I read this: Before the menopause, oestrogen is mainly produced by the ovaries.
If the ovaries are removed, or if they are stopped from working, there’s less oestrogen in the body to help the cancer to grow. This is ovarian suppression.
Thanks your reply! Mine is IDC and DCIS - ER and PR positive at 99% respectively and Her2-.
I’m just about about 2 years out from initial diagnosis. Had lumpectomy and radiation. No chemo but they were not able to get oncotype because they divide tumor into 16 blocks!
Samples are then too small!
And as might be apparent I still have my ovaries … hence my question. Thanks again for sharing.
Also … I’m taking tamoxifen as I didn’t tolerate AI’s. Initial diagnosis at 64 and no genetic connection.
What kind of radiation did they do on you and how many treatments?
Thanks, I guess I should take out ovaries then? Will I have to take another pill?💊. I don’t have my uterus.