Has anyone used all of three aromatase inhibitors to compare?

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sumomo
sumomo Member Posts: 49

Hi. Has anyone used all of three aromatase inhibitors to compare? Is rotating them a good idea? I guess finding the most suitable one to your body should be a good idea. By most suitable, I mean the least side effects, as you cannot know which one is most effective to you. Assuming the effectiveness is the same, the one with the least serious side effects must be the best aromatase inhibitor for you? So, my question is if it is common to try all of them, back and forth, to compare how your body reacts and eventually select one. And is it safe to do that, or better to stick to one?

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  • muska
    muska Member Posts: 1,195
    edited May 2019

    Hi Sumomo,

    Don't assume from the get go that you will get significant side effects from whatever AI your oncologist puts you on. Because most people don't get serious side effects. Also, side effects one might experience at the beginning often subside after a few months.

    Keep in mind that the purpose of all AIs is to stop your body from producing estrogen. Without estrogen your scalp and skin will get dryer, and you will probably experience some vaginal dryness too. I think you might expect this from any AI you take.

    As always, it is better to discuss the meds with your oncologist first who might have specific reasons to put you on a particular AI based on your history, other medical conditions or interactions with the other meds you might be on.

    Best

  • sumomo
    sumomo Member Posts: 49
    edited May 2019

    Hi muska,

    Thank you very much for your reply.

    I have already been on Femara. It's been a month, so it's very encouraging to read your comment about side effects subsiding after a few months.

    The reason I posted the question is that my oncologist actually suggested that idea. I decided to continue with Femara longer, but wonder if anyone else actually rotates every AI and compare?

    Thanks.


  • MexicoHeather
    MexicoHeather Member Posts: 365
    edited May 2019

    The AI side effects are variable. Some Oncologists say letrozole 2.5 mg reports the fewest side effects and start with that one. It made me dizzy and I felt body aches, so they switched me out after 2 months to Arimidex. Then there were hot flashes and generally the type of stuff your body would do if you stopped getting estrogen. I have backed down to 1 mg every other day and it's been tolerable. It's a very important part of my treatment plan, so I am keeping with it. I'm 51 now, so I have been on arimidex for over a year.

    I think it would be very safe to switch out, one to another, because they all are AIs. Sometimes you take a two week " holiday", let the drug leave your system and then pick up a different AI.

  • sumomo
    sumomo Member Posts: 49
    edited May 2019

    Hi MexicoHeather. Thank you for sharing your experience. I didn't know decreasing dosage was also an option. Good to know. I hope to continue with 2.5mg Femara as far as I can go, but not sure. I will see :)


  • Meow13
    Meow13 Member Posts: 4,859
    edited May 2019

    I took anastrozole and then exemestane, I found the side effects specifically joint pain to get worse over time. With anastrozole it got so bad after 18 months I couldn't take it anymore and switched to exemestane that eventually caused severe dry eye I had to quit. I definitely found side effects to be cumulative.

  • muska
    muska Member Posts: 1,195
    edited May 2019

    How one responds to such a medication is very individual. I am in my six year of anastrozole, never took holidays, never experienced any joint point (disclosure: I exercise regularly but it's not every day.)

  • Meow13
    Meow13 Member Posts: 4,859
    edited May 2019

    I was also exercise swimming doing 1hr 3.5 miles on the treadmill everyday did not make the joint pain any easier. Also the same dosage given to everyone. My height is 5' 3" weight 125lbs. I also do yoga, the pain had no bearing on my activity level.

  • Artista964
    Artista964 Member Posts: 530
    edited May 2019

    I haven't but my mo says arimidex and letrozole are similar so likely same same ses. Said the one that uses a different mechanism is anesterole (sp?). So letrozole was horrible for me and said the latter if I want to try again. But medicare doesn't cover it and it's too pricey for me. So I'm back on tamoxifen which doesn't really bother me. Better than nothing for my profile.


  • Meow13
    Meow13 Member Posts: 4,859
    edited May 2019

    Luckily now I have been off the drugs for 3 years the joint pain is really reduced although not gone. I never had any pain before taking this stuff. Before I enjoyed really excellent health.

  • pupmom
    pupmom Member Posts: 5,068
    edited May 2019

    Meow, you must mean before you got cancer you were in really good health. Nothing is the same after that event.

  • TwoHobbies
    TwoHobbies Member Posts: 2,118
    edited May 2019

    I have been on all three. I had some pain on anastrazole. Not really unbearable but my MO encouraged me to switch. Letrozole was about the same. She suggested I switchto exemetane and Iwas surprised that it is better for me. So you certainly can try others if you have issues.

  • sumomo
    sumomo Member Posts: 49
    edited May 2019

    Thank you all for your comments.

    Hi Rosabella. By anesterole, do you mean aromasin (exemestane) by any chance? I knew only 3 AI's, letrozole, anastrozole and exemestane. I didn't know about anesterole. Anyway, if Tamoxifen works well for you, I think that is good.

    Hi muska. It's great you have no problem for such a long time. Exercise must be helping. May I know how much exercise you do regularly? Do you take any Calcium supplement?

  • Artista964
    Artista964 Member Posts: 530
    edited May 2019

    yeah, aromasin.

  • muska
    muska Member Posts: 1,195
    edited May 2019

    I do an hour at a gym three or four times a week and also walk at least two miles most days. I don't take calcium.

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