Is there a test for vascular invasion?

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gcpommom
gcpommom Member Posts: 883

I have asked my onc numerous times, they keep telling me that there is no way to know if there is vasc invasion or not....I see others posting that they do know they have/don't have vascular invasion.  

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  • thenewme
    thenewme Member Posts: 1,611
    edited July 2010

    Hi Gcpommom,

    On my pathology report from the mastectomy, under the section called "Margins," mine says "Venous/lymphatic (Large/small vessel) Invasion (V/L) Present."  To be honest, I'm not exactly clear on what it means, specifically.  I mean I'm not sure whether it means I had both venous and lymphatic invasion present, or how they determine it. 

    Do you have a copy of your pathology report?  I'm interested to see what information others might have on this; maybe someone else can clarify.   Great question!

  • gcpommom
    gcpommom Member Posts: 883
    edited July 2010

    Hi!  Yes, I have a copy, but it doesn't mention any vascular results (I've gone through it many times),  so I too am curious if it is discovered via a blood test or what??  Thanks for responding : )

  • LRM216
    LRM216 Member Posts: 2,115
    edited July 2010

    My lumpectomy pathology report states "No vascular or lymphatic invasion."  I do not have any idea how they test it either, but I did read somewhere that the pathologist either sees capillaries coming out of the tumor.  I hope someone with a LOT more knowledge about this comes along to help you out with a much clearer reply.

    Linda

  • pj12
    pj12 Member Posts: 25,402
    edited July 2010

    I THINK when your tumor is microscopically examined by the pathologist lymphatic-vascular vessels can be seen... in the same way the type of cancer cells are observed and ID'd. In my case my  path report said LVI present.

    pam 

  • nmi
    nmi Member Posts: 180
    edited July 2010

    My mastectomy pathology report states "no definitive lymphovascular invasion is seen."  Then the at the end of report for staging-MX is listed, when I look that up, says no evidence of distance metastases.  I think they just could not definitively rule it out, but highly unlikely.

  • weety
    weety Member Posts: 1,163
    edited July 2010

    Try looking at this old thread.  It has lots of info on vascular invasion.

    http://community.breastcancer.org/forum/96/topic/737394?page=3#idx_75

  • gcpommom
    gcpommom Member Posts: 883
    edited July 2010

    http://www.google.com/url?q=http://community.breastcancer.org/forum/96/topic/709094&sa=X&ei=8eY3TJLrLN_tnQffx5T8Aw&ved=0CBgQrAIoAzAA&usg=AFQjCNHgerfgQ9e1Qd82U0Xc0LT5g7g7Pg

    After you click on above link, then just click on the link that says "The previous page is sending you to http://www.google.com/url?q=http://community.breastcancer.org/forum/96/topic/709094&ei=3e03TM6ALsLsnQfCpLD8Aw&sa=X&oi=unauthorizedredirect&ct=targetlink&ust=1278735589757561&usg=AFQjCNGtK63gEoVYscPZtGfavsbcj77uYQ

    For some reason, sometimes you cannot directly link to the older threads here, so this link is via google.  It looks like, from what I've read here, that vacular invasion is not done via a blood test, but is actually seen with/within the tumor itself, as Linda and Pam stated. 

    thanks to all, I will see if I can get a more detailed path report from my onc.

  • gcpommom
    gcpommom Member Posts: 883
    edited July 2010

    Weety:  we posted at same time, lol.  Your link brings up another confusing factor--how they sometimes state 'lymphovascular' invasion, versus just plain vascular invasion...it's so confusing.  I had negative lymph nodes, but that doesn't mean I didn't have vascular or lymphovascular invasion (I think)

  • weety
    weety Member Posts: 1,163
    edited July 2010

    Yeah, I don't understand it either.  My original biopsy stated that I did have LVI present, but then the mastectomy found no LVI present.  All the docs I've asked about it have said that it is impossible to look at every single part of a tumor, so in guessing about what was found on mine, the LVI must have been small and only in a small portion of the tumor (why it was seen in the biopsy tissue, but not in the mastectomy)  Still don't get it, though.

  • apple
    apple Member Posts: 7,799
    edited July 2010

    i think that once cancer goes into the nodes outside the breast area, the supraclavicular, mediastinal or axillary node on the other side,,.. they know vascular invasion is imminent.

    that was the case for me.

  • tibet
    tibet Member Posts: 545
    edited July 2010

    I think they can check it if there is a blood vascular invasion or not. I had mined checked after path was done just for whether or not there was a venus blood vascular invasion, nd they said there was no vascular invasion. In my path report, they also said there was no LVI but I had a tiny tiny spot in the sentinal lymph node.

  • Susie123
    Susie123 Member Posts: 804
    edited July 2010

    Confusing, but both are kinda right.

    Your path report will tell you if you had vascular invasion (in the sample that was removed).

    But, your nurses are right. There's no way to tell if some of the cancer cells broke loose and went to other parts of your body before it was found and removed from your breast. My onco's nurse told me to think of cancer cells as little folks that like to travel. Picture them with little suitcases getting ready to go on vacation, but instead of London and France, they're going to your liver, bones, brain, or lungs. At this time they have no test or scan that will pick up their presence until they set up housekeeping and grow larger. Nothing picks up individual rogue cells. That's why we all have to have some type of therapy after the surgery, just in case we have any rogue cells that are still floating around somewhere else. I take Arimidex every day to try and starve those little boogers just in case they're there. We never know.

  • thenewme
    thenewme Member Posts: 1,611
    edited July 2010

    I've been thinking about this issue, and wondering what implications it may have.  I think part of the confusion is the term "vascular," which technically includes both blood vessels AND lymph vessels.  Evidently, both are possible metastatic pathways but it's not so easy to understand and clarify the differences.  My personal conclusion is "... it's very complicated." LOL! 

    Here's an article that may help (although on my first read, it's clear as mud!)

     -Source HERE

    "In conclusion, we demonstrated that the described immunohistochemical technique made it possible to discriminate between BVI (blood vessel invasion) and LVI (lymph vessel invasion) in BC and enabled a more sensitive detection of LVI and BVI and a better assessment of the extent of both than on conventional HE stains. Furthermore, our data demonstrate that most (lympho)vascular invasion in BC is LVI and that lymph vessel tumour emboli are larger than blood vessel tumour emboli. This suggests that LVI and BVI are not just different routes of BC metastasis, but that both pathways are characterised by a different biology."

  • Jaimieh
    Jaimieh Member Posts: 2,373
    edited July 2010

    To confuse you even more it is also referred to as angiolypathic invasion.  I asked this question a long time ago but my oncologist said they look at the tissue to see if there is any evidence that cancer was in the blood vessels.  He said that if it is it leaves evidence that it was there. 

  • IsThisForReal
    IsThisForReal Member Posts: 384
    edited July 2010

    On the flip side, my path report says there is no evidence of vascular invasion.  However, 2/12 nodes were positive.

  • Luah
    Luah Member Posts: 1,541
    edited July 2010

    I had one sentinel node involved (micromets).  When I bemoaned the LVI on my path report, my BS kinda tossed it off and said you'd expect that with node involvement. But I guess almost anything goes...and I'm not sure how much weight you can put in it as a prognostic factor.  (I like to think not much!)

  • weety
    weety Member Posts: 1,163
    edited July 2010

    Mine was listed as "angiolymphatic" as well, which means "blood-lymph" !  I wrote a little bit above about my particular case.  There was evidence of vascular invasion "in a few small angiolymphatic spaces" listed under "vascular invasion/type" (this leads me to believe there are different types) and it was only found in the small sample they took the biopsy from.  The mastectomy DID NOT find any vascular invasion present.  I've asked each of my doctors a zillion times each, why it could be present in the small sample and not in the large sample, and the best understanding I can come up with is this:  the biopsy sample was small, so they were looking at a focused piece of tissue.  This found vascular invasion.  THe mastectomy sample was much larger, so they chose a couple of random pieces to focus on (slices that were stained and looked at under the microscope).  These pieces DID NOT have vascular invasion present.  My onc said that there is no way they could test every bit of the sample--they only look at so many slices, so in her opinion, my invasion must have been minimal and would have gone undetected if just the mastectomy was done, AND that this probably happens in many bc cases.  Aggressive cancers, especially, like to travel just like susie123 wrote about above.  And in aggressive tumors, they don't always wait till they are bigger to do so.  I hate thinking about all this.  But it is what it is.. . .

  • gcpommom
    gcpommom Member Posts: 883
    edited July 2010

    Wow, so confusing!  With my type of bc, metaplastic, the lymph nodes are not usually affected....MPBC tends to travel in the bloodstream rather than via lymph nodes, which is why I wanted to know if one could be tested for VI. 

    Jaimie:  Thanks for your input here....I just looked again at my path report, and saw the Angiolymphatic listed there (guess I had thought it just referred to lymph nodes, which I already knew were clean)....the 'angio' part refers to blood vessels, and my path report stated 'No angiolymphatic invasion'  so now I know,

    I agree with Luah as far as how much weight you can put in it as a prognostic factor, I was just wondering why my onc said it was not testable, when others here said otherwise...

    Thanks, ladies, for all of your input!

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