Changing to AI/OS from Tamoxifen after reviewing SOFT study?
Comments
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Exercise guru I would recommend trying the lupron first. I've been on lupron for a couple of years. My obgyn suggested taking out my ovaries. My MO said it wasn't necessary. The downside of lupron is getting the monthly shot and I supposed continued cost as opposed to surgery is a one time cost. If you want to go ahead with the ooph later then you can.
One downside I am finding of the lupron is they are not sure when I am in menopause and when to stop the shot. Has anyone encountered this issue yet?
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I am 54, diagnosed at 52, and at that point definitely pre-menopausal. I think that this is a very personal decision. My oncologist came to me with SOFT results as well. I was on monthly Lupron (HATED the SE's - abdominal and legs swelling, intensified hot flashes, general malaise for days - some women have no SE?) and Tam (no SE - felt great). She said that an AI would prevent recurrence more effectively for my ILC. Offered oophorectomy as best option for ensuring menopause, but affirmed 5 years of monthly Lupron otherwise. She claimed that there would be no way to accurately test for stopping Lupron any earlier. I could tell that Lupron was hard on my body. And all the SE/risks of oophorectomy seemed to be driven by menopause, which was my ultimate goal... So, I chose to be finished with the monthly chemical injections - a happy choice for me!
The SE's of the AI's have been very difficult for me - lots of joint pain, back pain, headaches, insomnia... My left knee swells to the point where I can not stand or walk... So, I may be headed back to Tamoxifen? I really value quality of life and standing and walking without pain would make life much more livable. I wish that I definitively knew the cause of my discomfort. I still believe that the oophorectomy was a good choice for me, avoiding those chemicals... I am sensitive:)
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twohobbies
there is really no way to know if you are in real menopause once you are on the shots other than stopping the shots - which you cant do if you are on an AI - I am on Tamox, stopped the shots in June and no period yet. I am hoping this is it because I really don't want to go on the shots again -
Daisylover, are you saying that your SEs are less with the ooph than on the Lupron? I was thinking that menopause is menopause but if that's the case, sign me up for surgery.
Rozem, have they done any bloodwork on you to determine menopausal status or are they just relying on your lack of periods? My dilemma is I recurred on tamoxifen, so tamoxifen does not work for me, and yet its bad to be on the AI if you are not menopausal. My MO did some bloodwork at the end of the month last month and I see her in November, so I'll see if she has any news when I go next time.
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I'm curious why some MO's are suggesting this, is it based on cancer type and stage at dx? My MO has said that if I just absolutely cannot tolerate Tamox than I should look into oophorectomy and then go on an AI, I wonder why this wasn't an option first? I'm worried about doing something as permanent as oophorectomy so I'm still trying to figure this stuff out.
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twohobbies I went off 2 years ago and they tested me a few months after and i was in menopause. A few months after that my period came back. Unfortunately if you arent close to natural menopause you can "snap" out of menopause. Thats why I dont think there is a safe way if you are young to just stop lupron and see what happens if you are on an AI. Thats one of the reasons why I stayed on tam. I couldnt tolerate the AIs plus i want to be able to stop the shots without the worry of no hormone therapy. If you recurred on tam then yes an AI is your best defence. If u are closer to natural menopause ask tour doctor if its safe to go off?
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I will be getting my first Lupron shot today then I am scheduling an oopherectomy the end of the month I am only 30 but after soft studies I can't not do it I feel like I must do all I can to keep this canver gone
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I was 43 at DX, 44 at surgery time, and premenopausal. Next week I will be having a full hysterectomy due to ovarian cysts. I didn't have chemo, but have been on Tamoxifen since the end of RT in February. My MO plans on the continuation of Tamoxifen. I am getting nervous about the approaching surgery, but I am ready to be pain free
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Annie88--I had my TLH/BSO in Jan due to ovarian cysts and thickened lining thank to Tamoxifen. I am staying on Tamoxifen for now since I do pretty well on it and my MO decided the 1 percentage decrease in recurrence risk wasn't enough for me to try AIs for now. It took about 6 months before everything settled down and other than some hot flashes (helped with iCool) I'm feeling pretty damn good! Hope it all goes well for you too!
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Be wary of those over the counter supplements. Most of them have herbs and plant based extracts which are estrogenic in nature, that is how they work. Many plants have estrogenic qualities.
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so on another thread some of the ladies brought up a very good point to me. My wife before starting chemo was still having her periods.. so basically she is in chemo-pause right now. She is only 40 years old. Her oncologist prescribed arimidex.... as others have pointed out... she isn't really menopausal. so how is the Dr. going to know if her ovaries "awaken" so to speak.
So options at this point are (still need to talk to him next appointment is on the 25th of November):
1) switch to tamoxifen
2) take an ovarian suppressor (IE Lupron) and arimidex
3) remove her ovaries and stick with arimidex.
no sure about having her ovaries removed.. based on her age. wonder about just an ovarian suppression with arimidex -
Amstar 15~
AI's, like arimidex, only stop the estrogen from being made in the fat, muscle, and adrenal glands. On an AI, her ovaries could still produce estrogen, so she could have a period. Does that make sense? I am trying to find an easy way to explain it.
I will say that I am 33 now, and after 4 rounds of chemo the Gyn doc said my ovaries were toast.
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TwoHobbies,
My side effects from the oophorectomy were negligible -- not sure if I had any? I definitely had fewer hot flashes after surgery. However, I do seem to have a lot of SE with drugs in general -- overly sensitive. I would believe that everyone is different in their reactions. It is good to read many responses with an open mind. The oophorectomy was the best choice for me. I have had many musculoskeletal issues on the AI's, so I have resumed Tamoxifen. I felt pretty good on Tamoxifen the first round. Lupron and AI's just were not good for me.
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Thanks Daisylover for the reply. Something to consider.
Amstar my doc measured my FSH levels and I showed no signs of menopause despite not having a period after chemo. I would see if that was measured. I don't know if it's good to be on an AI if you're not certain to be in menopause. At least that's what I have been told.
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Today we got an email stating her charts had been updated. Upon going in and looking at her results from her last blood work that was done I saw the following:
Estradiol (which is the main estrogen produced in the ovaries) her level was 5pg/ml and post-menopausal levels should be 0-50 - so check she is within post-menopausal range
Then on her FSH (follick Stimulation hormone) she is 74.6 MIU/ML and post-menopausal range is 23.0-116.3
So I guess as long as her MO continues to do blood work to ensure her ovaries haven't started back up arimidex maybe the way to go. Then I would assume that if they do start up then maybe Lupron would be discussed.
But then as others have brought up.. how do you know when her ovaries kick back in? If the blood work is done monthly.. maybe that's to much time in between? So what I am going to ask on the 25th of November is if she is post-menopause based on her bloodwork.. then why not just put her on an ovarian suppressor like Lupron just to ensure that her ovaries don't kick back on?
Who knew there was still so much even after chemo... heck she has her breast reconstruction on the 8th of December as well... a heart scan as well the 23rd of November (her 2nd scan since she was diagnosed in May 2015)
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Does anyone know how Lupron and menopause were determined in the TEXT and SOFT studies. I would want to make sure my MO was following the same protocols.
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This may be a dumb question but....do either the SOFT or TEXT study apply to someone already in menopause? And, if so, are the percentage results different for post menopausal women? I was pre menopausal when diagnosed and treated and then had a hysterectomy in Jan so now am post menopausal. My MO debated swapping me to an AI but decided since Tamoxifen was fairly easy on me and that I would get "no significant benefit" from switching, that he would leave me as is. Are there any hard numbers for women like me?
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Hello,
I do not post often, but felt the need to share my frustration with recommendations based on this study. I am post menopausal due to a hysterectomy when I was 39. I have been on tamoxifen for 4 years after local recurrence ( or new primary - dr. not sure because grade and er status different) 6.5 years after mastectomy for high grade dcis . I have been told for this entire time that I would not be put on AI because I am only weakly er+ (14%) and too young (47 now) and the risk would far outweigh the benefit for someone like me. Last November when I saw oncologist he did talk about remaining on tamoxifen for 10 years but again dismissed idea of AI, which I responded to by saying that was good because I had no intention of going on one because it appears I would have very little benefit and a whole lot of downside potential. Fast forward to annual checkup yesterday during which I saw new pa in practice and she said the plan is now to put me AI next year for 5 years. WTF?? All of a sudden the weighing of side effects to benefit no longer matters? From what I can tell, those in the study who gained the most were premenopausal women. There is really not much positive effect from those who are menopausal already and taking tamoxifen. My other gripe is how does it figure for someone who is so weakly positive. It has been explained to me that tamoxifen works no matter what % of positive but AI effectiveness is directly linked to that percentage. So basically, I would get very little benefit with the possibility of all side effects. When I asked pa about this she acknowledged it was true but went on with her spiel. I just wonder if individual stats even matter when a study like this comes around or do all docs just feel the need to get on band wagon so they won't be accused of under treating. Sorry for rant, but so frustrated.
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Kadyann - remember that you get to make your own treatment choices. You need to weigh your understanding of the research and what your Drs are telling you - and decide what is the right decision for you. And you have the right to second and third opinions. I was on the cusp of the benefit age for SOFT and was further out of treatment than the research cohort - so I questioned their initial recommendation that I shut down my ovaries and move to an AI. I went and got lots of other opinions and eventually decided to just stick with tamoxifen for the full 10 years. And i feel good about my decision. Lots of drs are pouncing on this research and making very aggressive treatment recommendations for women where it is not necessarily warranted - in my admittedly non-medically trained opinion. You have to learn what you can and then make the best decision for you. Good luck!
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Kadyann, I ditto, Ramols. I think some forget they are their for us and need to present all the options, benefits and cons. I fully understand they are the experts but please don't try to put me in a bucket without explaining why and the net effect on me! period! I had to tell this to my MO recently. Took her by surprise but she opened up after that.
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Good on you ladyb1234, I'm sure when my Doctors see me coming they say "Oh no, not that nosey old woman again" haha! They forget it is all about me and I have the right to hear everything, even if I don't understand everything.
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Hi. I'm new to the forum. I was diagnosed with IDC stage 1, grade 1. I've had a double mastectomy and am now on Tamoxifen. My allred scores are 7 Estrogen, 6 Progesterone. I don't know my percentages. My Oncotype score was 16 or 17. My tumor was less .8 cm (tiny). My sentinel node was clear. My question is - Do I really need to take tamoxifen? It makes my ribs hurt and I'm very tired and depressed. Also, my upper back and neck are sore. I feel like I am cancer free, but the pain makes me nervous. What is the true (number) benefit of Tamoxifen with my stats. I know lots of people take it with no issue. I feel guilty if I don't. Anyone else go through this?
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CRYAN, first, welcome to our community. This is a difficult question to answer. What does your treatment team say about your questions. Here is a page about Tamoxifen that you may find helpful: http://www.breastcancer.org/treatment/hormonal/ser...
Let's here from others!
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I'm feeling the same about Tamoxifen, started off great with no side effects but now my feet are killing me, I'm walking like a little old lady. I've thought briefly about stopping taking it but decided I couldn't live with myself if I had a recurrence and feel I have to do everything possible to avoid this. I failed taking Letrozole/femara because the side effects on that were even worse than tamoxifen
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Such a tough and very personal question, CRYAN! We have so many tough decisions to make on this trip (I call it a trip, rather than a journey, if you get my drift). My MO used an example of someone with stats similar to yours--tiny 3mm tumor, low grade. She did not take any endocrine therapy and had a recurrence to her bones. He scared the daylights out of me, and so I am taking it for at least 5 years, and he said more likely 10 years to life (feels like a sentence!) of some sort of endocrine therapy. I had an Oncotype score of 17 as well, but grade 2. I've been off Tamoxifen for 2 weeks for my surgery, and I am not looking forward to starting it back up again, but I will!
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Cryan- I too have had some issues w/ Tamoxifen. There have been neck, headaches, and insomnia. I changed to the Teva generic brand a week and a half ago and no more symptoms. I am not sure if it was the change or if it is mind over matter.
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123Justme-
Your link refers to POSTmenopausal women. The SOFT trial and other studies are PREmenopausal.
For premenopausal women, ovarian suppression and an AI were the most effective combination for preventing recurrence.
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Correct. However, some post menopausal women are on Tamoxifen as well as some pre menopausal women are on AI's.
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off to get oopherectomy no turning back now menapause here I come
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