LVI (Lymphovascular Invasion)

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Sadlynew2018
Sadlynew2018 Member Posts: 222

I can’t get a real clear answer on what this is and how much it factors into things re prognosis. All I’ve read is how it corresponds to a poor prognosis (Dr google strikes again). The internet makes it sound like a death sentence. Ugh. Are there women out there with LVI that have good stories? I know, Dr Google is the enemy.

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  • InnaB2018
    InnaB2018 Member Posts: 1,276
    edited December 2018

    Hello, SadlyNew! Thank you for starting this thread. I also hadLVI and my doctors are all very optimistic about my prospects. They said to not trust Dr. Google. Let’s hope more people will show up with positive stories.

  • bluepearl
    bluepearl Member Posts: 961
    edited December 2018

    LVI is fairly common. There is "extensive LVI" which is far more of concern than "focal LVI". The latter doesn't really have a significant effect on overall survival nor cancer specific survival from what I have read in oncology journals. What matters most is the biology of the tumour. Your grade 3, at 3cm, didn't go very far so suspect a better biological profile for that one. Grade 3 doesn't always equate with extreme aggressiveness either. There are women aho have grade 3 and a very low oncotype. Be well. Hoping the best for you!

  • windingshores
    windingshores Member Posts: 704
    edited December 2018

    I am glad you posted this!

    I had LVI and am starting my 4th year of treatment with Femara: so far so good in terms of cancer.

    I had a grade 3 (one hospital said grade 2), highish ki67%, contradictory HER2 results (finally resolved as negative with a higher number of cells counted), mixed ductal and lobular.....and LVI, which was "focal" and specifically seen in lymph vessels.

    But my Oncotype was 8. My doctor had it retested!

    I had 4 different oncologists in 4 different hospitals in those first months. The two main ones were so chirpy about my prognosis that I barely trusted them. The third one said "I don't blame you for being troubled," and did the retest of HER2 and Oncotype and offered me chemo or whatever else I wanted. I said no to chemo with that Oncotype because I figured it wouldn't work anyway.

    So, back to LVI. Google claims that LVI is equivalent to one positive lymph node. None of my doctors has said that about focal, but there is very little info on focal versus extensive. My doctors did make that distinction.and were reassuring, as was my surgeon (The Oncotype recommendation for one lymph node wouldn't have been different anyway. )

    My understanding however is that it isn't so much about where the cells are but more about the type of cancer cells we have, which, as my favorite oncologist said, LVI proves "want to go somewhere." (My surgeon said the location of cells was not relevant and made motions to show me that they wouldn't be better able to crawl out just because they were located nearer the armpit!)

    I believe everyone had cancer cells circulating so I resolved not to worry about the image of escaping cancer cells. But I do worry about having cancer cells that were able to move and settle somewhere. Which means they have the capacity to spread.

    Also, think about it: they found LVI present but how many people have LVI that is not detected (and do fine)? There is really no reliable way to test the consequences of LVI because there is no way to be certain it isn't present- unless the pathologist is able to look at every single vessel, including those outside the surgery area. Am I wrong?

    Anyway everyone tells me my prognosis is good, and so far, it seems to be. If your tumor responds to estrogen and progesterone, all the better.

    Genomic Health, the maker of the Oncotype test, says that 30% of grade 3's have low Oncotypes.

    This cancer business is so much more complicated than people think :)


  • Sadlynew2018
    Sadlynew2018 Member Posts: 222
    edited December 2018

    thank you everyone :-) I had a second opinion on diagnostic from MDA. They put me at grade 2 and found mixed lobular and IDC. Ugh. Oncotype is 27, which is intermediate/high. A google search of LVI is just plain frightening. I’m 90%ER positive and 70%PR. Can’t wait to get on an estrogen blocker. Planning to have my ovaries out after treatment is over. If it produces estrogen, I want it out. Maybe it will be my present to myself on my 42nd birthday. Ugh.
  • L-O-R-I
    L-O-R-I Member Posts: 114
    edited December 2018

    Hi Sadlynew2018,

    I have a thought for you.  Instead of Googling LVI (Lymph Vascular Invasion), look up ways you can improve your Lymphatic System.   There are a lot of things that you can do to improve your prognosis, along with the Doctors' recommendations that you choose to follow.  If your lymph system is healthy, your estrogen and progesterone will be better regulated, amongst several other benefits.  I find it distracting and even enjoyable to rise to the challenge of becoming healthier.  Why not feel better and look better while going through this journey!

    Lori

  • Beznaranca
    Beznaranca Member Posts: 9
    edited December 2018

    Hi everyone. I have some doubts about tumor biopsy findings prior to surgery, PHD findings after surgery, and PHD finding on the tumor site 2 months after surgery. Here's the finding one by one.

    Biopsy 2 weeks before surgery said:

    Size: 25mm

    Grade:2

    ER 100%+, PR-, HER2-

    Vascular component - there is no

    In situ component - there is no

    KI67 - 54%

    PHD after my operation said:

    Segmenter mastectomy of block 4.5*4*3.5cm dimensions.
    Inferior surgical limit 1.6cm, anterior 0.3cm, posterior 1.3cm, lateral 1.5cm. Medical surgical limit 2cm distance, tumor size 2.3cm.
    Gradus: 3
    Necrose in invasive tumor: no
    Peritumoral lymphatic/vascular cavity inventory: no
    Surgical limits: there is no tumor
    Tumor's nearest surgical limit: anterior 0.3cm, superior 0.6cm
    No metastasis in sentinel and 7 more lymph nodes
    Ki 67 - 61%
    Er - 100%
    Her 2 neg
    Pr neg

    We've done a revision of part of the tumor 2 months after the operation and it said:

    Size of a sample: 1*1 cm

    ER - 100%

    Her2 - negative

    PR - negative

    Grade: 2

    Lymph - vascular invasion - yes

    Ki67 - 44%

    In situ component - no

    Let us know this part for the lymphatic vascular invasion and tumor grade. Who to trust? Biopsy, PHD after surgery or PHD revision? What is the lymphatic vascular invasion at all, is it despite the good sign that the tumor is not in the lymph nodes?

  • windingshores
    windingshores Member Posts: 704
    edited December 2018

    Well, yeah, my biopsy results said HER2 + and I bought a wig and baking soda for my mouth after chemo etc. 

    Pathology after surgery was negative, equivocal, then negative with a count of higher number of cells.

    I had differences in grade at all 4 hospitals, some 3 and some 2. That really isn't significant, according to doctors and I don't give that much thought.

    I am not saying that I don't trust pathology. But I was told the HER2 with biopsy may have been from having proportionally more DCIS cells versus invasive cancer cells in the sample, and DCIS tends to be more HER2+.

    And I heard somewhere that if a post surgery sample has some tissue where the biopsy was done, it could look like LVI because cells get dragged around. Sorry I can't remember specifically so don't go by this rather vague info. Main idea is that there can be things that affect pathology results that we don't know about.



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