Second opinion recommends OS + AI. Dont know what to do

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Hi all! I started Tamoxifen in November after BMX and diagnosis of 3.2 cm ILC and .3 LCIS beside it. Oncotype score was a 14 so no chemo. I've been worried about the size of the tumor and that it was located in the inner mid quadrant so had a second opinion regarding treatment. She said she would recommend OS and AI due to the size of the tumor. Main doc does not agree to switch. I've read a lot on the soft study but still not sure what to do. Has anyone been through something similar or advice on whether one would be more effective? Thanks in advance!

Comments

  • Cpeachymom
    Cpeachymom Member Posts: 518
    edited January 2020

    Hi Heather-

    I am on OS plus Tamoxifen. What reason did your main doc (MO?) give for not agreeing with the other doc?

    Luckily I was able to get my second opinion at Dana Farber, so my MO was willing to defer to them. She has even reached out to them when I was having trouble with Lupron and we were figuring out next steps.

    You could switch docs if you don’t get satisfactory answers . I have read here that AIs are more effective against ILC.


  • HeatherT75
    HeatherT75 Member Posts: 3
    edited January 2020

    He kept referring to a study done comparing the oncotype scores and endocrine therapy and that because my score was a 14 I wasnt fitting into the table, even if he took the other MOs concern about the tumor size. Both of the centers I went to are comparable as far as reputation and ratings so I'm sure that helps him not feel like he needs to entertain the idea.

  • Cpeachymom
    Cpeachymom Member Posts: 518
    edited January 2020

    Hmmm, maybe he could show you the study? My Oncotype was also 14. It seems when you don’t fit into their normal range, they don’t know what to do. I was young, large tumor, positive node, etc, and my docs actually pushed me to get a second opinion because they were all in disagreement.

    Could you switch to the second opinion doc if you want? I’d rather have someone willing to work with me than someone who’s going to dictate my treatment.

  • JRNJ
    JRNJ Member Posts: 573
    edited January 2020

    HeatherT75, I have similar dx. My onctotype was 15. I went for 3 opinions, because I wanted to be aggressive. Dr. 1 Not sure about chemo, tamoxifen for a few years, than AI, but wanted me to go for more opinions. Dr. 2 said no to chemo, tamoxifen for a few years, ovaries removed, than AI. Dr. 3 (Sloan) said yes to CMF chemo and right to AI, but use Lupron for ovarian suppression. AI's supposed to be more effective. I have read tamoxifen not always effective for ILC. Dr. 1 agreeable to Sloan recommendations, with some alterations. I am doing CMF chemo, radiation, ovary removal, than AI. My ovaries have super powers. I'm 54, CMF chemo is supposed to cause menopause. I've had 2 periods since 12/2 on chemo. They have to come out.

    cpeachymom, no one has recommended Tamoxifen with ovarian suppression to me, but I see you and a few others doing it. What's the thinking behind that, I thought Tamoxifen was for pre-menopausal? But I have ILC, so Tamoxifen supposed to be less effective.

  • Cpeachymom
    Cpeachymom Member Posts: 518
    edited January 2020

    Hi jrnj- It was explained to me that there is a risk for incomplete OS. It has happened to someone on these boards, so not just hypothetical. AIs can’t handle that much estrogen, and in fact will increase your risk if you’re not surpressed. ( I don’t know how ) The fact that I see all these premenopausal women on OS + AI whose MOs are Not checking their estrogen levels makes me cringe. If docs are monitoring regularly, then it makes sense.

    Anyhow, this was the recommendation from a doc who specializes in BC in young women at Dana Farber, so my MO was willing to follow the treatment plan. It seems like a middle of the road option.



  • JRNJ
    JRNJ Member Posts: 573
    edited January 2020

    omg. You can’t trust any one dr. There are too many options and opinions. Sloan said OS and AI. I told her I wanted my ovaries out and she said not necessary. My gut told me I’m not relying on a drug to suppress ovaries. I think that’s the plan for me, ovaries out and AI, as I read tamoxifen is not always effective on ilc. But you have me thinking.

  • ShetlandPony
    ShetlandPony Member Posts: 4,924
    edited January 2020

    This post will be brief and without the links I would normally find for you because I am tired and getting ready for a “procedure" tomorrow.

    Anyway, the Oncotype RSPC (recurrence score pathology clinical) is an online tool your onc can use to personalize your Oncotype score by taking into account your age, tumor size, proposed treatment etc. If the revised score is higher, there is a vote for being more aggressive by using OS + AI.

    However, what concerns me is that there is evidence that some ILCs are resistant to Tamoxifen, and that the difference in outcomes with tamoxifen vs. aromatase inhibitors is much greater with ILC as opposed to IDC. One paper to look at is from the BIG-98 study. There is a clinical trial currently recruiting that compares tamoxifen, aromatase inhibitors, and faslodex for early stage ILC. They are conducting this trial because they have enough evidence that ILC may respond differently than IDC to standard endocrine treatment. Also there are questions about how reliable Oncotype is for premenopausal ILC when it was validated with mostly postmenopausal IDC patients. See the threads here on the LobSig test, not yet available. By the way, in premenopausal women tamoxifen can raise your estrogen (get it tested), and that can't be good.

    Bottom line, I would choose the OS + aromatase inhibitor.

    ShetlandPony (Oncotype 16, diagnosed premenopausal)

  • JRNJ
    JRNJ Member Posts: 573
    edited January 2020

    Thanks Shetland. I mentioned it to my new BS, that tamoxifen might not work as well for ILC, and she made a little face, but it doesn't matter, my plan is ovaries out and AIs. And I also agree, I am very skeptical of the oncotype, especially for node positive pre-menopausal. To be honest, the whole Oncotype thing has me skeptical. You see them recommending harsh chemo for small tumors with no spread to nodes, because they "respond well" to chemo, but don't recommend it for node positive, with LVI and extracapular extension. But I know that comment is opening up a huge can of worms, lol......

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