Do MRIs accurately predict node involvement/non-involvement?

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PiNKiDC51
PiNKiDC51 Member Posts: 61

All -

Trying to figure out if there is a way to determine if nodes are involved prior to surgery. One survivor in another forum referenced that she learned via an MRI. Has anyone else learned this way? If so, how accurate is the MRI in determining nodal involvement? In other words, if the MRI shows nodes are clear, does that mean that the pathology reports will also come back showing negative involvement? Has anyone had an MRI show nodes are clear, but then gotten a positive pathology report after surgery? Thanks!

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  • DiabeticCancerChick
    DiabeticCancerChick Member Posts: 30
    edited January 2016

    I have, yes. The MRI showed the tumor with 4 bright spots surrounding it (the 4 spots turned out to be non-malignant), but it did not show node involvement. During surgery, 4 sentinel nodes were removed and analyzed immediately by a pathologist, who found no cancer cells present, so no further nodes were removed. A more thorough analysis after surgery showed that a micromet (about 0.9mm) was present in one of the nodes. Because of that, I had chemotherapy, when up to that point everyone expected that hormonal therapy would be all that was necessary. So you never really know until the final path report after surgery. And that report is only done on the nodes they have removed... even if those nodes were clear, it is unlikely, but still possible, that cancer cells have migrated to nodes that were left intact.

  • PiNKiDC51
    PiNKiDC51 Member Posts: 61
    edited January 2016

    DiabeticCancerChick-

    Thanks! I sort of suspected it was a possibility. I'm trying to avoid expanders and the facility here pushes hard for them because of what could come back on the pathology report. By the way, do you know if you were given a stronger chemo because of the micromet?

  • SpecialK
    SpecialK Member Posts: 16,486
    edited January 2016

    My MRI did not show node involvement, but I had two positive nodes.

  • ksusan
    ksusan Member Posts: 4,505
    edited January 2016

    My MRI suggested but couldn't confirm node involvement (the node was positive on surgery).

  • ElaineTherese
    ElaineTherese Member Posts: 3,328
    edited January 2016

    I had three scans before beginning neoadjuvant chemotherapy: an ultrasound, which showed a suspicious node, a PET scan which showed a suspicious node, and an MRI which showed a suspicious node. That node was also tested via fine needle biopsy, and it was found to be cancerous. So, prior to chemo, my doctor staged me at Stage IIIA because of the tumor size (over 5 cm.) and the nodal involvement (at least one node). Hope this helps!

  • muska
    muska Member Posts: 1,195
    edited January 2016

    My MRI was clear before surgery and there was no suspicion about nodes involvement. Post-surgery results are in my profile below.

  • MsPharoah
    MsPharoah Member Posts: 1,034
    edited January 2016

    Hi, I just wanted to add that my clinical examination and the US and MRI imaging found no nodal involvement and that was the same result after surgery. While I was waiting for final pathology and worrying, of course, I did a lot of research. When an MRI sees no evidence of nodal involvement, it is about 80% accurate. I hung on to that during the waiting process. But as the ladies above state, nothing compares to the pathological examination of removed tissue. Good luck in your treatment and if the MRI says no nodal involvement, hang on to that!

    MsP

  • DiabeticCancerChick
    DiabeticCancerChick Member Posts: 30
    edited January 2016

    Hi PiNK,

    To answer your question about whether I was given stronger chemotherapy because of my micromet... I had chemotherapy ONLY because of node involvement. Had there been no sign of cancer cells in my node, chemotherapy would not have been recommended. Also, my rate of cancer cell division (Ki-67) was quite low, and since chemotherapy targets the most rapidly dividing cells, it meant that chemo was of little benefit to me. But node involvement made me do it anyway. As to strength of chemo, well... that's another story. I was originally supposed to have Taxotere-Cytoxan therapy, but my oncologist was on vacation during my "chemo teach" (orientation) and first infusion, and during the chemo teach I casually let it be known that I would never, under any circumstances, agree to take dexamethasone. They use dex with every chemo drug, and they decided that the risk of severe edema was too great to allow Taxotere without dexamethasone, so they switched me (under the care of another onc I never met) to Adriamycin and Cytoxan. Adriamycin is cardiotoxic, and has a lifetime limit, since heart damage can appear years and years after taking it. Turns out I was supposed to get 250mg total, but instead I got the lifetime limit of 421mg. So far so good, but we'll see. The moral of my story is: find out exactly what you're getting, if you get chemo, and see if it makes sense. I got a full dose of something that has a small, but not invisible chance of causing permanent heart damage, and the benefit of it is statistically smaller. And I could go on with the screw-ups I experienced during my surgeries, so my advice to you is Pay Attention. Little things like your oncologist being on vacation and another one stepping in are not always little things.

  • jojo9999
    jojo9999 Member Posts: 202
    edited January 2016

    Pik,

    My nodes showed clear on US and MRI - they call it "clinically node-negative". Sentinel lymph node biospy found a 2mm micromet in one node. BS said MRI can't really dedect cancer that is under 2mm. Even with the positive node, I was not given chemo due to low oncotype score. Although the Onco test was originially only given when node negative, it is now routinely used when there are 1-3 positive nodes. However, I received radiation because of the node, so immediate construction would have been compromised. I had expanders, fills then radiation, then exchange.

  • Jinx27
    Jinx27 Member Posts: 238
    edited January 2016

    My MRI overestimated one axillary node and one mammary node. My BS biopsied the axillary node and it came out negative. During surgery the mammary node was not seen as "enlarged" as it was on the MRI therefore it was kept in tact. Chemo is recommended for me though. My profile gives details about other node involvement I don't believe those nodes showed up on the MRI at all.

  • PiNKiDC51
    PiNKiDC51 Member Posts: 61
    edited January 2016

    JoJo9999: Okay - So for the most part, I get that there's not going to be a way to predict nodal involvement before surgery - which SUCKS!! There neeeeeeddddssss to be some way to tell that BEFORE surgery. If there's no nodal involvement, I don't have to have radiation or chemo for treatment. So, IF I knew that for sure then I could safely pick Immediate vs. Immediate-delayed reconstruction, which is what I MOST desire to do. I am VERY FRUSTRATED at the prospect of having to have those stupid expanders. I'm mortified at the single picture (my choice as seeing surgery images - well, I don't have the stomach for it) I've seen at my PS office of the mastectomy and expanders right after surgery. I DO NOT want to be that scarred and FLAT. I do not believe that they are just for 3 months - I see no evidence after I hear of necrosis, capsillary contractures (spelling??), infections, and the like that keep women in these things for 6 or 7 months or longer. And, I DO NOT know how to get past this expander thing and every time I try to figure something out - it's a no. (Sorry for the rant!!)

    Anyway, since you wrote about it I wanted to ask - what is the difference between the Oncotype DX test different from the genetic test? One article I read it seemed to me that the Oncotype DX test is done at surgery, but maybe I misunderstood. I had thought the genetic test was what was needed to learn about potential recurrences . . . are they one and the same test or different??? If the Oncotype DX is done at surgery and tells whether a woman needs chemo - what's the point of a genetic test once diagnosed?? Thanks for the help from someone who's tired of trying to read and assimilate so much data - often my mind is fried and I'm still trying to work and function in everyday life. I'm really trying not to let this take over my life, but that seems like it's almost impossible some days! Aaaarrgghh!

  • PiNKiDC51
    PiNKiDC51 Member Posts: 61
    edited January 2016

    DiabeticCancerChick:

    I hear your frustration! I feel it almost everyday now. It's only on days that I just say that I'm not going to deal with this now, that I find some relief. However, I'm soon not going to have that option as I'm going to have to very soon line up my surgery and begin all the "FUN" all you other women have already begun or have just finished. I'd so like a time machine with the knowledge I have right now. I'd so do an Angelina Jolie - though I'd not go the implant way. However, as much as so much of the mastectomy concept itself sucks - having to consider radiation/chemo as possibilities and those affects . . . sucks even more!!!! And, having to try to absorb all the different aspects of treatment - well, I think any woman who goes through this should get some sort of education/medical certificate. Anyway, thanks so much for your reply!

  • jojo9999
    jojo9999 Member Posts: 202
    edited January 2016

    Pink,

    I hope someone might chime in to explain the OncoType test better than I can. It is a genetic test of sorts, done on the tumor itself. It looks for certain characteristics of the tumor, including ER, PR, her2, Ki67,and others - basically genetic characteristics of the tumor that are thought to influence recurrence. When you say "genetic test", are you referrirng to testing for BRCA1/2? That is a test done using your blood or saliva, not on the tumor.

    About reconstruction, a few things. I have seen photos of immediate reconstruction and the women looked very beat up! no way to avoid that. If you end up not needing radiation or chemo, you can have the exchange fairly quickly - just make sure to ask your PS. Each one has different policies on how long to wait. My PS said at least 6 weeks after radiation. (I waited 12 weeks). Some PS insist on at least 6 months after radiation. I understand your frustratio, especially with all the strides they have made with skin-sparing mastectomy and such in the world of plastic surgery.

    Come to think of it, I had my sentinel biopsy done about 5 days before my mastectomy. So I knew going into the BMX that I had a positive node. If you could do that, then you would know what other treatments would be needed and whether or not you should do immediate or expanders??

  • Denise-G
    Denise-G Member Posts: 1,777
    edited January 2016

    My full-body MRI showed most of my 9 positive nodes - however, my sister's did not. They thought she had perhaps 4 positive nodes so

    they biopsied them before surgery. After surgery, they found she had 13 positive nodes. Her nodes were very small and clumped together.

    Mine were larger and easier to see.

  • PiNKiDC51
    PiNKiDC51 Member Posts: 61
    edited January 2016

    Denise-G: Thanks for sharing! Quick clarification - So, your sister had a SNB prior to her mastectomy/lumpectomy surgery? And, it was during this surgery that they found 13 positive nodes OR she had an SNB and they found 4 before the mastectomy/lumpectomy and then found more after/during the mastectomy/lumpectomy? Currently, I am being scheduled for a SNB prior to my mastectomy.

  • PiNKiDC51
    PiNKiDC51 Member Posts: 61
    edited January 2016

    jojo9999: Last post of the evening as I should've been in bed a long time ago. Yes!! I did learn about SNB and chatted with my BS today about that and am being scheduled. So, hopefully in about a week after the test I'll know if I have positive nodes or not to know if I'll have to go the expander route or not! Keeping my fingers and toes crossed that I can actually get some good news from this test. Not holding my breathe after all the news I've gotten lately, but trying to look towards the positive (according to the BS about 90% of women at my stage with my markers have no nodal involvement).

  • Pilgrim64
    Pilgrim64 Member Posts: 16
    edited January 2016

    just curious, were you offered oncotype testing?

  • Pilgrim64
    Pilgrim64 Member Posts: 16
    edited January 2016

    no, my MRI said no node involvement but sentinel node biopsy was positive for 1 out of 5

  • Artista928
    Artista928 Member Posts: 2,753
    edited January 2016

    The only way to know if nodes are involved is at surgery. Not everything shows up on MRI necessarily. MRI showed I had no node involvement and my tumor was 4cm. I had 1 node involved and there was a string of cancer cells leading to a 3 cm tumor which surprised the surgeon, so I had 7 cm of tumor--it was dumbbell shaped and buried nicely.

  • etnasgrl
    etnasgrl Member Posts: 650
    edited January 2016

    My MRI showed no node involvement and my surgical oncologist told me that while only surgery will determine it 100%, it was "promising".
    In my case, the MRI was correct. The cancer had not spread to the lymph nodes.

  • PiNKiDC51
    PiNKiDC51 Member Posts: 61
    edited January 2016

    etnasgrl - So, happy for you as that makes things so much easier!! Unfortunately, I opted for a SLN Biopsy and learned that I do indeed have lymph node involvement on the left. This is so disappointing as it now seems to rule out immediate reconstruction. Maybe I'll learn something new to put it back on the table, but for now it seems to be off. Next up appears to be meeting with a MO.

    Good Luck with your treatment!

  • StaceySue2U
    StaceySue2U Member Posts: 281
    edited February 2016

    Pinki, I'm sorry to hear that you have lymph node involvement. Did they say how many nodes?

  • PiNKiDC51
    PiNKiDC51 Member Posts: 61
    edited February 2016

    StaceySue2U - On the left 3 of 3 sentinel nodes showed involvement. On a positive note a 2nd area in the left breast turned out to be benign, so that opened the possibility of a lumpectomy on both sides, and thus the ability to go through all the treatments (chemo/radiation) without the expanders I didn't want. After I've healed, if I'm too nervous to stay with just the lumpectomies, I can have the mastectomy and immediate reconstruction. I will most likely opt for this option cause while lumpectomies and mastectomies are supposed to be relatively equal with regards recurrence chances with a lumpectomy there's a 10% chance of local recurrence while with a mastectomy it's a 3% chance.

    DiabeticCancerChick - Re-reading this strand I saw your reply to my question about chemo again. Currently I am being recommended for an AC-T, and while I'm not as up on chemo stuff yet - I did recognize that I'm being recommended for the same treatment you ended up with (and my ki-67 is also very, very low). The alternate if I can't take that, my backup protocol is supposed to include that Taxotere-Cytoxan that you were supposed to get. As I read that Taxotere causes permanent hair loss in some women, I've decided I will now allow that drug to be administered. However, re-reading your post, I am concerned about the AC-T protocol as I have mild regurgitation in 3 of my values according to my preliminary echo. My question is, it sounds like you did some research on these different drugs. Are there any that aren't a risk to the heart and/or other organs. They are all poison - is there a way to get a "better" one? I do have a bunch of questions for my MO though cause I am wondering with being able to have radiation and hormone therapy is there any medical proof that someone with my low ki-67 gets any benefit from chemo that outweighs all the different risks. Anyway, just wondering if with your research you determined something else would've been a better protocol for you (since we seem to have the same type of markers I'm curious what you may've learned that I don't know yet)? Thanks!

  • reflect
    reflect Member Posts: 576
    edited February 2016

    My MRI showed enlarged nodes (but the first radiologist to read it did not notice). A fine needle biopsy of two nodes was positive.

  • isnogard
    isnogard Member Posts: 34
    edited February 2016

    Hey thanks diabetic.... I was given another ultrasound for my lymph nodes and did not get the same doctor that had been giving me ultrasounds. So, I got another doctor who did not look at my pathology report but did look at my MRI scans and the ultrasound scans and gave me a morbid review of my prognosis. I knew he didn't look at my pathology report because he couldn't tell me details about it ( I had to tell him). I thought it was un called for for him to give me bad news that I already knew about. His tone of voice was morbid. I was so upset after leaving. I hope the oncologist I see on Tuesday about chemo gives me better details about my prognosis.

  • Christine7
    Christine7 Member Posts: 8
    edited February 2016

    Not sure if I am in the right place, new here. Diagnosed DCIS grade 2 in November 2015. All this fun stuff happened right after I had my base mammogram at 35 which showed a suspicious cluster of calcifications. Ultrasound and MRI showed clear of anything else. No family history and BRCA negative. Lumpectomy last Friday found out today 6mm stage 1 tumor hiding in there Another node in there was tested negative, but she wants to go back in for more nodes to be sure in 2 weeks. Find out last pathology results this Friday about receptors. Chemo and radiation not sure about until then. And to think if waited until I was 40 to have a mammogram. But the stress of all this is taking over me. Being strong in front of 3 little ones is hard. Thank goodness for a strong husband

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

    Hang in there, Christine7. Indeed, be thankful that you didn't wait until age 40! Once you know more, you may want to jump into another, more specific forum, including that for younger women. We are truly sorry that you find yourself here, but hope you find comfort in our community, and know you are not alone!

    Hugs,

    The Mods

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