Concerned about the side effects of anastrozole

Posted by tinalove @tinalove, Jan 31, 2016

I completed all treatments for breast cancer but now I am supposed to take hormone blocker, named anastrozole. im concerned about the side effects. Has anyone here taken it and did anyone have hair loss?

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@mjpayan

Hi Karen. Protocol from what I know is 5 or perhaps 10 years on Arimidex or other AIs. 2 years in. Able to live with diff affects. Had my bone density test on Monday. We will see.

Glad you are doing well.

My second time around. Tamoxifen the first time. Put me on menopause within months at the age of 48.

I’m good.

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I’m glad you’re doing well and I wish you continued good health!

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In reply to @guntherbear "@mollymiller" + (show)

I am on Aromasin. I have tried Tamixifen and Arimidex and could not handle the memory loss with them. I have joint ache with aromasin and have gained 30 lbs. But I found out that working out 5 days a week for 20 minutes has really helped with the joint ache and I also lost some weight. I had a double mastectomy and I am half way thru my 5 years. Oh and I average 32 hot flashes a day 😔. But I feel the side affects are way better than cancer recurrence 😊@mollymiller

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@mollymiller

Best wishes, fellow Arimidex friend! I find that the Arimidex symptoms vary. Some days are pretty pain-free. I'll stay with it for the whole regimen with the hopes of no reoccurrence and wish the same for you!

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@karenrbach

I am a 14 year breast cancer survivor. My Oncologist had me on arimidex (or generic) 13 years. He retired and my new oncologist discontinued use of this drug last year. She said protocol was 10 years. I am fine and never really had any side effects from this drug. I have had a bone density test every two years to make sure all is well. I consider myself fortunate I never had any of the side effects being described.

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Hi Karen. Protocol from what I know is 5 or perhaps 10 years on Arimidex or other AIs. 2 years in. Able to live with diff affects. Had my bone density test on Monday. We will see.

Glad you are doing well.

My second time around. Tamoxifen the first time. Put me on menopause within months at the age of 48.

I’m good.

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@karenrbach

I am a 14 year breast cancer survivor. My Oncologist had me on arimidex (or generic) 13 years. He retired and my new oncologist discontinued use of this drug last year. She said protocol was 10 years. I am fine and never really had any side effects from this drug. I have had a bone density test every two years to make sure all is well. I consider myself fortunate I never had any of the side effects being described.

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You are a fortunate woman on several levels!

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I am a 14 year breast cancer survivor. My Oncologist had me on arimidex (or generic) 13 years. He retired and my new oncologist discontinued use of this drug last year. She said protocol was 10 years. I am fine and never really had any side effects from this drug. I have had a bone density test every two years to make sure all is well. I consider myself fortunate I never had any of the side effects being described.

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@elizm

to @gwinter and @cindylb -- My path report for BC was Stage 1, ER positive, HER2+++; ovaries were removed about 10 years ago.

Not to complicate your lives, but here are a few notes from my experience. European oncologists test hormones all the time. It is not standard for American oncologists. I asked mine why that was and was told that each test only gives a reading for that point in time, and that the amount of circulating hormones changes frequently. I suppose that makes sense... I'd still like to be tested and he's not going to it.

Another note: check each of your meds and supplements as to their interaction with hormones. In my case, I was taking a diuretic called spironolactone; it decreases circulating estrogens and androgens. As soon as I started on the anastrozole (I have chosen to take only half a dose/day), I incurred very sore cysts in my breasts and on my ribs. When I switched diuretics, the soreness and cysts disappeared. The oncologist was clueless. Thankfully, I have a GP who works with me. I also take 1,200-2,000 IU of mycillized D3 each day for bone health and learned that it, too, decreases circulating estrogens. There are a number of factors affecting our hormones (and quality of life), and we each must root those out and make them part of the conversation with our oncologists. HUGS!

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Very true on the hormone tests only showing that moment in time on your hormones but my levels have stayed consistent with the past 6 tests. I am post menopausal (by quite a few years now) and I think once you've reached that 'milestone' the levels stay pretty consistent. If you can't get an oncologist to test your hormones, perhaps your GP would be willing or an OB/GYN. No harm in watching those numbers to get a baseline. I think hormones are so overlooked over a woman's lifetime and such a big contributor to so many diseases and conditions. Hugs to all....

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@cindylb

Hello fellow Stage 1....
I had lobular (not ductal) cancer and so opted for a bi lateral mastectomy because my Stage 1 came after a Stage 0 and I'd already tried lumpectomy. All that said my risk is about the same as yours for recurrence. I tried 3 of 4 hormone drugs (Arimidex, Letrozole and Tamoxifen). With all three I had serious side effects including joint pain, depression, stomach issues and finally (my final straw), during the 3 months of trying all these drugs I got Shingles and mono. My body doesn't like any drugs, let alone these. I had to opt NOT to use the hormone drugs. They tell me if it comes back I have to use them and I suppose I will but I was so miserable and ill on them it didn't seem worth it given the chance of recurrence.
SO................I finally asked my oncologist WHY DON'T YOU TEST WOMEN'S HORMONES? And the answer was that they 'assume' all breast cancer women will be on the drugs anyway so there is no need. They tested my hormones at my request and I had so little estrogen naturally in my body that they were actually concerned that I had no estrogen (I have estrogen positive breast cancer). I had never had Progesterone or it was very, very low (hence the over dominance of estrogen by whole life) which had caused me multiple problems throughout my life. I have had the on going estrogen and progesterone tests (as well as Testosterone off and on) for 3 years now and I have no hormones to feed the cancer.
I'm sure the meds do things other than simply erasing hormones quickly from your system that are advantages for keeping breast cancer at bay but I opted to be monitored more closely and feel better day to day.
AT THE VERY LEAST........ASK YOUR DOCTORS TO DO A BLOOD TEST TO GET YOUR HORMONE LEVELS. It's easy, quick and gives you a snapshot of your hormone activity. There is a more advanced hormone profile that can be run as well that I had done during menopause (for Stage 0 breast cancer) which showed an estrogen dominance off the charts. That was a urinalysis and some blood work and was done by a homeopathic doctor my open minded oncologist at the time suggested. I learned a lot there too about acidic vs alkaline body type, diet and safe supplements to stop cancer. In my case it didn't work but perhaps slowed it down a bit. Also, I lost 30 pounds along with diet changes following my mastectomy. Hormones are produced in fat and can aggravate the levels and contribute to cancer. Another thing I learned is that many skin care products contain PABA and that can mimic hormones in your body. I use a lot of lotion (live in a dry climate) and I have changed lotions, shampoos and other products to limit my exposure. None of these changes have impacted my life greatly. In fact, most (losing weight, diet, careful use of products, etc) have actually improved my health....no nothing crazy there and nothing lost.
We are lucky we were diagnosed at a low risk stage. There are no guarantees that we won't get cancer again but you have to consider how you feel today and whether you can enjoy your life.
Finally, I still worry every day (a little) and lots when I come up on my six month check ups that not taking the pills was a mistake but they just made me feel too sick. You are not alone.......Some of us just don't tolerate the 'usual' treatment. P.S. I am about to be 61 and was diagnosed first at Stage 0 at 56 years and Stage 1 at 58 years.
HUGS............
Hugs to you!

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Yes, I worry "a little" (lot) about recurrence, but I turned down chemotherapy. Stage 2A EST receptor positive, age 68 and it was just something that I did not want to do. Statistically the change in life expectancy was small. Arimidex is my "Dumbo's Feather"....Each day I take that little pill and think it is going to keep my cancer at bay.

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Happy for your input! Informative.

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