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MyWalk_113
MyWalk_113 Member Posts: 6

Hello. I just had my surgery and will see my Dr in a couple days for post op, at which time I will receive my pathology report. He wants me to have 6 wks of radiation therapy. I know you are not Dr's , but I don't understand why I should receive radiation if they got clean margins (which I won't know until I go in). This has been a rough go physically for me. I am epileptic, and had 2 bad seizures the night I got home from surgery. I am still in quite a bit of pain, I wasn't prepared for how much cutting they did. I have a problem with brittle bones, and I really don't want to weaken my body with radiation unless it's absolutely necessary. Also, I write and meditate a lot. Still can't shake the sadness. I think it will get better after getting the pathology report. I'd appreciate any thoughts. Thank you.

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  • ChiSandy
    ChiSandy Member Posts: 12,133
    edited January 2016

    I had the same questions about radiation and endocrine therapy after my lumpectomy path results came back with clean margins. The reason is that even with negative nodes and clear margins, one can never be sure that there are no residual “micrometastases” in either the breast or elsewhere in the body, to continue growing and become either a new tumor or distant metastases. So there are two types of postoperative “adjuvant” treatments: local and systemic. Unless you are well past 70, and had extremely small DCIS, if you had a lumpectomy you will almost certainly be advised to have radiation, as “local” therapy. It is designed to directly destroy those micromets most likely to remain after your tumor was removed: the ones still hiding out in your breast. Depending on how aggressive your tumor, its size and location and your age, you might be offered a shorter course of higher intensity partial-breast radiation, to just the tumor cavity and a small margin around it. Radiation is usually not given if you had a mastectomy--but it’s still administered if there were positive lymph nodes and/or tumor cells found on or near the chest wall.

    You might also (probably most of us almost certainly) have some micromets that made it past your lymph nodes and into your body. Therapy to kill them is called “systemic.” If your tumor had a certain profile that indicated it was likely to be aggressive, and/or your OncotypeDX (if needed & offered) score confirms it, then you will be urged to have chemo--since cytotoxic (cell-poisoning) drugs given as chemo are most effective in killing those fast-dividing (and thus aggressively-growing) cells. If your tumor’s profile indicated it was slow-growing and was positive for estrogen & progesterone receptors, and/or your OncotypeDX (if needed & offered) indicated it was non-aggressive, you would be advised to go on endocrine therapy. Hormone-receptor-positive tumor cells are too slow-growing to be vulnerable to chemo drugs, and the risks to you from chemo would outweigh the benefits. These tumor cells feed on estrogen. So instead of “slash/burn/poison” of surgery/radiation/chemo, your treatment plan would be “slash/burn/starve”--by depriving tumor cells of estrogen they would starve to death. Why, if these cells are so slow-growing and non-aggressive in the first place, would you even need to kill them in the first place? Because, given enough time untreated, they could still grow and spread to your bones and organs, eventually killing you. It’d just take a long time. And some tumor cells, even if hormone-receptor-positive, have more aggressive features (e.g., Grade 3, spread to more than a couple of lymph nodes, large size, HER2 positive), you would get chemo first to kill the most aggressive cells, then radiation to kill what’s hiding out in your breast, and finally endocrine therapy (5-10 yrs) to starve the slow-growing stragglers to death before they can become a tumor and spread.

    Endocrine therapy will depend on how close to menopause you are (or if you’re past it). If you’re not done with menopause yet, you’d get Tamoxifen and maybe some other drug to shut your ovaries down permanently or temporarily. If you’re postmenopausal, you won’t need anything to suppress your ovaries; and instead of Tamoxifen--which blocks access to the estrogen receptors--you’d get an aromatase inhibitor, which neutralizes the enzyme that helps your fat cells and adrenal glands convert the hormones they make into estrogen. There are other considerations your doctor will explain more fully. It’s still your call, but you need to know why certain treatments are recommended for you so you can make an informed rather than just a visceral decision.

  • MyWalk_113
    MyWalk_113 Member Posts: 6
    edited January 2016

    Thank you for all the information and insight... I truly appreciate all of it! ChiSandy, you gave me exactly the information I was looking for, thank you. I am 55 , went through menopause at 31, after I had my last child. I go to the Dr in 2 days, at which time I will find out what my pathology report says. Thanks to all in this group, I just want to know!! Hug

  • Moderators
    Moderators Member Posts: 25,912
    edited January 2016

    Glad you are finding the support you need, MyWalk! Please keep us posted on your path report when you receive it. We're all here for you!

    --The Mods

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