How much does hormonal treatment reduce risk?
Hi all,
I am going in next week to see my MO to decide which hormonal treatment I will be starting on. I've been reading threads but get so overwhelmed by it all. I was originally going to start on Tamoxifen as I was pre-menopausal, but decided to go ahead and get the hysterectomy out of the way first. My bone density scan showed I already have osteoporosis in my hips (I'm 48) and I have high blood pressure and hypothyroidism as well. There is a strong family history of cardiac issues. It seems that there really are no "good" choices, and that anything I take is going to cause other problems. My oncotype report said I have 13 percent chance of recurrence with hormonal therapy. It doesn't say what the risk is without it. I'm wondering if hormonal therapy reduces my risk enough to make it worthwhile? My potential for complications seems rather high. I know that everyone is different, but I'm wondering if anyone has been in similar situation and can offer advice? I don't want to blindly take what the MO suggests without having done some homework.
Comments
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Definitely ask your oncologist. I believe it is based on many factors. I was shocked how little benefit it was providing to me specifically.
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Thanks Meow13, I guess I'll see what the recommendation is. I just worry what happens when we start throwing more and more meds into the mix.
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Take a look at this thread; the question you asked about what your risk will be if you don't take hormone therapy is discussed:
https://community.breastcancer.org/forum/78/topics/872175?page=1#idx_24
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Thanks Beesie, I looked at the thread. Based on the approximate 30% reduction provided by Tamoxifen or AI's, I figure my risk of recurrence without them would be about 19% or so, with about an absolute reduction of ~6%? I hate that so much of this process is "playing the odds." I've been given so many statistics since this process began. Of course we want the best odds we can get, but it all really seems like a crap shoot!
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Yup, that's what I would estimate too. It's still important to talk to your MO, but now you have a number in your head that you can ask about - and if your MO gives you a very different number, you can ask why.
We really are playing the odds through all of this. Obviously, the lower the risk that something bad (mets, for example) will happen, the better. Yet even if there is only a 1% chance of developing mets, that means it's one person out of 100, and someone is going to be that 1 person. On the other hand, if the risk of something bad happening is really high - say 95% - it still means that 5%, or 5 people out of 100, won't have that bad thing happen. Any one could draw the lucky straw and be in that group of 5. So either way, it is very much a crap shoot.
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So I saw my MO and agreed to start taking Arimidex. Never really got a straight answer about how much risk reduction it would give me though. He also said he would like to start me on Prolia injections because of my osteoporosis. Of course I came home and started reading about Prolia and now I really don't want to take it. I can see how this stuff can really start to snowball after a while.
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I never saw any statistical study conclusions, it is like it is automatically assumed you will do hormone therapy. The one tool, cancermath, said in my case I could expect a 1% risk reduction taking AI drugs.
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Whatjust, sometimes it is best to step away from so many opinions on these boards, and just listen to your doctor. At least give yourself the chance to try it your doctor's way. I was in a similar position, except for the blood pressure and thyroid issues. I take Tamoxifen, and was scared just like you. I had the support of my MO and several women on here, to just try the Tamoxifen. I was eased into the medication, per my request and am doing amazing. I had my uterus and ovaries out, prior to starting. I have osteopenia in my hips and alot of dental work in my mouth. I am in my third year of taking it!!!
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Michelle, I agree with you that sometimes it's best to listen to the advice of our doctors - they are the experts, after all.
That said, what raises a question to me in Whatjusthappened's case is that her doctor didn't give a straight answer to her question about how much risk reduction she would be getting from Arimidex. We need the best information possible to make our decisions, and every decision is a balance between benefit (risk reduction from the treatment) and risk (health issues that might arise as a result of the treatment).
Whatjusthappened, can you get a second opinion? From what you describe (cardiac issues, osteoporosis) it sounds as though Tamoxifen might present fewer risks, but this is something that a MO should be discussing with you in detail, comparing the AIs to Tamoxifen with consideration to your other health issues. And you should not be expected to start endocrine therapy, which presents you with these health risks, without understanding how much it will reduce your risk of mets. Risk tolerance is very personal, and you can't make the benefit vs. risk decision without this information. Any responsible MO should discuss this with you.
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I agree with Beesie at the very least your doctor should advise you armed with statistics, risks, etc. Mine came from my Oncotype report.
My MO prescribed Arimidex initially because I was post-menopausal but I also had osteopenia. Arimidex attacks the bones. I was on it one year until I questioned her about it given my osteopenia why I was taking a drug that worsened my condition. She switched me to Tamoxifen. Damage was already done. I should have said something sooner but shouldn’t she have known?
I respect the expertise of the medical profession but I also believe we need to be our own advocates. They aren’t used to being questioned about their advice much less opt not to take it but the bottom line is it’s our bodies, our lives and we are entitled to a QOL even with a BC DX.
Diane
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Agree with Beesie and edwards750, we are our own best advocates.
Asking those questions is completely appropriate and your MO should be glad you are a full partner in your medical treatment.
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Thank you guys so much for the replies. I am listening to my doctor, which is why I agreed to start the Arimidex, and I am easing into it with the understanding that I call if there are any problems at all.
Bessie, I did ask if Tamoxifen might be a better choice, and he said that now that my ovaries are out, the AI's offer a better risk reduction (based on ATAC study) and even Tamoxifen would weaken my bones to a degree. I don't really feel like he was evading my question about the degree of risk reduction, he just said that because my cancer was strongly receptor-positive, the AI's would offer a significant benefit, esp. considering my age, and the recommendation would be that I take them. I think he was hesitant to give me a number because he disagreed with the 13% risk of distant recurrence cited in the report, saying that because we have already taken prophylactic surgical measures, that number would be lower now. Originally, he said the AI would bring my risk from 13% to less than 5% before I pointed out that the 13% was WITH anti-hormonals. Which launched a big conversation about where that number came from. I eventually gave up on trying to get an actual number. It sounds like it would just be a guess anyway.
Michelle, was the reason you started Tamoxifen because of the osteopenia? Just curious. It seems like your doctor maybe had a different opinion about it.
Meow13, I think it IS assumed that everyone will do hormonal therapy. I would love to see some studies on risk without the anti-hormonals, but I'm sure it would be hard to find volunteers for those studies. Still, 5-10 years ago, I would have gotten chemo for the same diagnosis, even though it apparently would offer no benefit at all for me. So progress is being made!
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With the normal caveat about everyone being different and everyone's cancer being different, I'll offer my wife's experience because it sounds somewhat similar to your's, Whatjusthappened. When her IDC was diagnosed in 2016, her MO strongly recommended chemo and hormone treatment. This combo would supposedly reduce the risk of recurrence from about 16%-18% to about 10%-12%. My wife had reservations about the side effects of both the chemo and the hormone and opted out of each: it just seemed to her that a 6% to 8% improvement wasn't worth the potential complications involved with chemo or hormones.
Well, here we are 3 years later and my wife now has MBC in both lungs. It was found early (and by accident), and she's now on hormone treatment (Femara and Ibrance). Obviously just because this was the diagnosis for my wife doesn't mean it'll similarly happen to anyone else, and we're trying to look forward not backward. Everyone has to do what they think is best for them (as my wife did), but since you asked for similar situations, I thought I'd share my wife's experience. Good luck with your decision. I know it's not easy.
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Thank you ladies for encouraging me to advocate for myself. I am slowly learning that I need to be very direct with my questions- I have always been afraid of offending someone, which seems ridiculous, but there it is. What I think I'm going to ask for (very directly) is a referral to an endocrinologist before agreeing to biphosphonate drug.
BLMike, I am terribly sorry to hear about your wife. Thank you for sharing her experience and providing a reality check about what's at stake.
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Meow13, I tried the cancermath tool. It showed me to have a 10% risk reduction using endocrine therapy. Pretty significant, though I'm sure not as accurate as the oncotype report. Ok, I'm done running numbers- I've been obsessing way to much!
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I posted the below a while ago. Personally, I believe that trend of less deaths and increased 5 year survival rate has to have correlation to AI’s and Tamoxifen. Surgery has been around forever. Radiation has been around forever. Many of the chemotherapy drugs used have been around forever. The AI’s/Tamoxifen are newer as are the biologics that are being used for people who develop metastatic disease. I have to believe that less people are developing metastatic disease as a result of the AI’s/Tamoxifen.
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Whatjusthappened,
I just had a conversation with my MO to try to pin down the benefits of endocrine therapy for me, since I've been having a very hard time tolerating the tamoxifen.
One thing she was adamant about was that oncotype does not predict the impact of hormonal therapy. It assumes hormonal therapy, and predicts the impact of chemo. She did do a backwards extrapolation, basically an increase of 30-50% of my listed oncotype risk. But still, she she insisted on the principle.
It's kind of frustrating that there's no testing to predict the impact of hormonal therapy for any specific individual (based on their own physiognomy, or tumor profile, or whatever). Hopefully in the not too distant future there will be. But for now I think it is like the earlier days of chemo, where everyone has to do it just in case we are the ones that will have the big impact, even knowing that for many people it might have no impact at all.
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Yeah the MammaPrint test is slightly more geared to overall risk. But the assumption is that you'll do hormone blocking therapy.
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Whatjusthappened, you comment about CancerMath showing a 10% risk reduction seemed high to me. I just put in your data, and came out with very different results. So you might want to redo your numbers.
Of course CancerMath is a general program and less specific to you than the Oncotype test, but what CancerMath did say that is relevant is that an AI would reduce mortality by 32% at 15 years.
Doing the backwards math, this means that if your risk of mets is 13% with an AI, based on your Oncotype score, your risk would be 19% without taking the AI. This is completely consistent with all the studies I've read about AIs providing approx. a 1/3 risk reduction, relative to mets/mortality.
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Hi Beesie, I ran it again and it gave me a 30% mortality rate at 15 years without AI's vs a 20% mortality rate at 15 years with AI's. So a 10% absolute reduction. But a 30% or 1/3 rate of reduction, which could be extrapolated onto my oncotype risk, since that is more specific to me. So I figure the 19% without AI's is probably the most accurate number I'm going to get.
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SimoneRC, those are interesting statistics. It makes sense that if death rates are decreasing, that the use of endocrine therapy is playing a big role. That makes me feel a bit better, actually.
Salamandra, the answers your MO gave you seem pretty much in line with what I have seen discussed here and in other threads. I guess hormone therapy is assumed because of how well they target receptor-positive cancers. I'm sorry you're not tolerating the Tamoxifen, since your particular options are probably limited by your age. What we need now I guess are better ways of dealing with the side effects that estrogen suppression can cause. Maybe I'll be one of the lucky ones who aren't plagued with SE's. Keeping my fingers crossed, and developing a deep appreciation for those who have had to make these decisions!
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