Aromatase Inhibitor and just walking away.
Comments
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Artista...so happy you are doing well on anti hormone therapy. Yes, some do and some don't. Those who do well have a completely different perspective on it. I'm not disputing that it can lower your recurrence risk. However there are no guarantees. Many have recurred while on it. So its just not that black and white. Especially when it affects your QOL negatively. Good luck to all navigating this complicated disease.
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Artista, Coming from a perspective of side effects versus a recurrence. My quality of life was so poor on the Aromatase Inhibitors I would have to be stage 4 before I would consider them again. I had no life on the drug. I no longer wanted to live I was so miserable. It effected my vision, my hearing, I couldn't sleep, I was depressed, it was all I could do to get out of bed each day and do something. I tried to exercise while on the drug and I was too exhausted. I was hurting my pets. I would say awful things to people. I do think everyone should give it a try some do well, some don't. I did get the blessing from my MO to stop. I am working on diet and exercise right now as my alternative. I am down 7 pounds and I have been increasing exercise. Both of which are important in reducing recurrence.
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Brutersmom thanks for the encouragement, maybe I'll get a blessing too instead of a guilt trip
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Letra was horrible for sure, which an AI would have been better for me to be on that Tamox. Just thankful Tamox isn't so far. My thinking is while I know there are no guarantees that at least I have done what I can tolerate and won't have the should have thoughts that I know I'd have. If one's profile screams at least give it a try like mine then why not try and see if you can tolerate it. Should I recur or mets I won't be kicking myself about AIs because they debilitate me. I have bad arthritic knees that I think Tamox is even making it worse but as long as I can survive I'll stay on it and whatever else that may come up in it's place in the future as my onc seems to think within the 10 years I'm on this that something else will come along.
And diet and exercise is important. I'm trying to lower my caloric intake due to my inactivity but that's hard when food is your bf. But why not do everything you can. With someone with my profile, I'd rather pop a pill in hopes rather than let it go and deal with stage IV chemos and misery daily until the end.
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Artista, yeah I know that it sounds like some of us are whining. I could continue to hack the joint pain, it's my eyes that I'm worried about. I don't know what my probability is like some. Had an occult primary and one node with 3mm of cancer found after surgery. Plus 35 radiation treatments. ER/PR 100/40 Her neg. grade 3, IIA. I see MO and Opthamologist in a week
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marijen we are not whining. At least most of us. These are powerful drugs with fairly devastating side effects for some of us and I'm not talking about joint pain, tho that can be pretty disabling.
We do the best we can. None of us want to relapse. But some side effects are immediately more serious.
Live and let live. I love the comments that say "I have been on an AI for 4 weeks and I feel great!"
So did I up until a year
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Yeah I thought I was doing great too for two years almost.
I said "it sounds like" but you are right the sides can be very serious and then we get another medicine for the sides that has sides!
It's a very hard decision to make when you're in-between, but in my case I fear that if I go on my eyes will end up damaged and requiring surgery. And then it will be too late
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Artist yes your correct your profile sure does scream at least try the tamoxafin. For me it was really doable. IDC responds better to it than lobular which I have. I'm really hoping you'll be able to handle it.
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And please don't underestimate the psychological effects of estrogen deprivation. Insomnia and depression often go hand in hand. It's difficult to "bounce back" when one is dealing with that on top of overall aches and pains.
I am wondering if anyone has noticed their scalp is cracked or dry as a result of AIs. My head has been so itchy and I even opened a bleeding sore on my head- sorry if I'm being gross. Any recommendations for how to relieve the dryness? -
After being off arimidex for 6 weeks, my liver function is back to normal. I wonder if my oncologist will believe me now
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Yeah...Arimidex is definitely not a *happy* pill... I already have issues with anxiety and depression. But, staying on this for as long as MO wants or forever - if that's what it takes....
Edited to Add: if I wasn't so high risk for going to stage 4...not sure I would stay on this for the long term..
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Scared I hear you
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My MO seems to feel something better is coming down the pike so possibly those on the 10 year or more plan will be relieved with something that's not so riddled with se's.
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Hi, I am new on this particular discussion thread. I just switched from Nolvadex (Tamoxifen) to Anastrozole a couple of weeks ago... I am on pill 12. I might be having more hot flashes, not sure. I had crazy insomnia coming off Tamoxifen but it seems better now. Not great, but better. Anyway, I have a weird question that is bothering me... I had very bad vaginal dryness on Tamoxifen, but now I am almost normal in terms of lubrication like I have not been in over two years. Is this abnormal?Does it take time for vaginal dryness to develop when you switch? Or, is it possible that I am still producing too much estrogen? I am 53 1/2, have not had a period in 30 months, my FSH has ranged from 33 to 53, but while on Tamoxifen, my estradiol levels were running very high (which I have read can happen to some women, and that you cannot get an accurate reading on Tamoxifen). How much time do I need to give for those levels to drop now that I am off Tamoxifen and on an AI? Really, really hoping to avoid an ooph or Zoladex shots for a variety of reasons.
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Hi Falconer,
I woke up from surgery with the itchiest scalp. For 6 months I looked like a dog with fleas. Had sores that wouldn't heal (yuck). Finally went to the dr and she said I had cradle cap (ha, maybe surgery was a "rebirth"). Anyway, she said to use Selsum Blue with selenium sulfide. Worked like a charm
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Lucky# thanks for sharing the cause and the cure. I did have surgery 8 weeks ago, so maybe the same happened to me. I see the dr next week; I'll ask.
Funny you mention being reborn. I had DIEP Flap recon, and when my Dr peeled the tape off of my new belly button I had the same response. Sometimes these metaphors can help us see BC as a way to start over... -
Artista...thats the best news I've heard in a long time! Any more information on new anti hormone treatments?
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dtad- No. She just didn't feel that somewhere in the 10 years that I'm to be on AI or Tamox that something better isn't on the horizon. So nothing affirmative, but she is into research too so who knows.
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marjen and others: please discuss the vision issues with ophthalmologist; not just with MO. I am not sure what vision issues/problems you are referring to but if it is cataracts (known SE of some of the drugs) then the surgery is one of the easiest out there, with very, very low risks of complications, and the truth is: cataracts are common enough that you probably would need to have the surgery at some point regardless (though the anti estrogen drugs can make the cataracts worse or lead to earlier onset). And, almost always the surgery solves/cures the vision problems, so I am not sure how it could be 'too late' once that happens.
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Octogirl, it's not about cataracts, I've already had surgery. It's about PVD - Posterior Vitreous Detachment.
Breast Cancer Medications and Vision: Effects of Treatments for Early-stage Disease
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205820/#!po=12.2093
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That's something I've never heard of, marijen. I'll read the article you posted. This disease and its treatments - it's like an octopus the way it touches so many seemingly unrelated parts of your body!
MJ
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I never heard of it too until a friend sent it to me after I mentioned my PVD. They do say side effects include blurry vision. It's a money maker, think of all the women on AI. Another reason they want us to take it forever? My vitreous has already detached, luckily a clean break but that doesn't stop future eye problems.
My opthamologist was eager to read it, I brought him the link. I see him again in two weeks
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Here's a link for
Retinal Hemorrhages in Anastrozole Users
http://journals.lww.com/optvissci/pages/articlevie... -
Everyone should read this it's very long but worth it
Anti Estrogen Side Effects
http://www.musclechemistry.com/upload/bodybuilding... -
thanks for the link, marjen; I hadn't heard of this either but will also read it and discuss with ophthalmologist. I do get extensive vision testing fairly often as I have a retinal problem that pre-dates bc, so I imagine he will be interested in seeing this.
Octogirl
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octogirl, you're welcome. I try to share new things I've found
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Here is an excerpt from the last link I posted. Who knew Letrozole was non-suicidal and it should be tapered off?
Estrogen rebound: This is one of the Letrozole side effects that are perhaps the worst out of the two non-suicidal aromatase inhibitors (the two being Letrozole itself and Arimidex). While Arimidex exhibits issues of Estrogen rebound, Letrozole has shown to exhibit far worse rebound upon discontinuation. This side effect is very important to understand. It is a side effect generally unique to both Arimidex as well as Letrozole (Femara). The third major aromatase inhibitor, Aromasin (Exemestane) does not exhibit Estrogen rebound. This is because Arimidex and Letrozole are what is known as non-suicidal aromatase inhibitors. Aromasein (Exemestane) is a suicidal aromatase inhibitor. A suicidal aromatase inhibitor (such as Aromasin) indicates that once it has bound to the aromatase enzyme (and thereby inhibiting it), the inhibited enzyme remains bound to aromatase permanently, rendering the enzyme inactive forever. The body will eventually manufacture more aromatase enzymes, but the current bound enzymes are bound indefinitely, eliminating any risk for Estrogen rebound.
Non-suicidal aromatase inhibitors such as Arimidex and Letro, however, are only bound to the aromatase enzyme for limited time periods before the aromatase inhibitors unbind either due to natural metabolism, or through competition with other substrates. If a non-suicidal aromatase inhibitor is halted too abruptly, the circulating inhibited aromatase enzymes that have not been metabolized out of the body will then become free again, and begin aromatizing androgens into Estrogens at an often rapid rate. This is why it is advised to slowly halt administration of Letrozole, and/or slowly reduce the dose and/or frequency of the dose when stopping. Often times the inclusion of a SERM such as Nolvadex starting several days prior to and following the cessation of Letrozole will be necessary so as to keep the breast tissue receptor sites blocked from any possible Estrogenic activity that results from the rebound, after which Nolvadex administration is halted as Estrogen levels slowly return to baseline. -
I still think they should measure estrogen levels from the beginning. There are also articles that say the AI can stop working after a period of time. Maybe estrogen shouldn't be decreased to nothing. I don't know.
My intent is not to scare but to inform.
KB870, you're welcome too.
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marijen, thank you for all your informative articles. I had never heard about tapering off letrozole if discontinuing it, I will remember this when the time comes.
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I went cold turkey off Letro after 5 weeks. Maybe if it was a lot longer it would have been different but I immediately felt better with all my se's from it gone in a couple days, what the half life is.
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