Lymphatic invasion

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Kate2z80
Kate2z80 Member Posts: 66
edited February 2017 in IDC (Invasive Ductal Carcinoma)

My surgical pathology report stated that there was "lymphatic invasion identified", but all lymph nodes were negative.  I'm waiting on the Oncotype test results, but was wondering if anyone had seen any articles or studies on the need for chemo in the face of this finding.  I have found articles saying that lymphatic and/or lymphovascular invasion are unfavorable prognostic indicators as far as recurrence, but I haven't seen anything addressing how much weight should be placed on the finding of lymphatic invasion in deciding on whether adjuvant chemo is appropriate in a Stage I, negative lymph node scenario.  My oncologist said that lymphatic invasion findings are very unreliable, but that some oncologists consider them to be on par with a finding of one positive lymph node.  My doctor is predicting a low Oncotype score, which is great, but I want to consider all reasonable treatment options and considerations to avoid recurrence and I'm not comfortable basing my decision entirely on the Oncotype test result.

If you have found any articles or research on this topic, I'd appreciate a link or citation. 

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Comments

  • TenderIsOurMight
    TenderIsOurMight Member Posts: 4,493
    edited July 2009

    This is a complex question in many ways, isn't it? I take it the lymphatic invasion was seen by the pathologist when viewing the breast tumor microscopically, i,e., the pathologist did a special stain or grossly saw breast cancer cells in local lymphatic channels.

    I always understood that vascular invasion requires a special stain also, unless it's heavy in its involvement or what pathologists call "gross" i.e., large. 

    I too have heard that lymphatic invasion in the tumor may be on par with one positive node.

    This is a very personal choice. You could hit it hard the first time because of this finding with chemotherapy and hormonal therapy. You could await the Oncotype DX and see where the score lies. You could see if the Ki-67 (cell division marker) is high (above 20) or low in the face of a low score. If the Ki-67 tends toward 20, and the score returns 18 or close too it, this may elicit a re-discussion of chemotherapy.

    You're oncologist and you sound like you work well as a team. Maybe you wish to go talk with the Pathologist who read your slides or ask your oncologist too. 

    Such a question is best answered by the experts you have and your comfort and research with them. I applaud you on your due diligence in your care.

    Tender

  • Kate2z80
    Kate2z80 Member Posts: 66
    edited July 2009

    Tender:

    Thanks for your post.  Is Ki-67 something that will be addressed on the Oncotype report?  I won't have it until next week and I've never seen one before.  Is it pretty self-explanatory and/or is there a website which helps a patient interpret it?  Do you know if the Oncotype test/report will address the issue of lymphatic invasion?  I know my oncologist said he would go over it with me line by line, but I don't see him until 7/27 and I will probably have the report a few days before that since he said he'd send it to me.  That gives me about five days to obsess . . .

    I'm going to drop a line to the pathologist.  The surgical path report was very brief on the lymphatic invasion seen and I would like more information.

    I hope more of this is clear once the Oncotype report is back because I have been researching this issue extensively online and haven't found much, other than that lymphatic invasion is a poor prognostic indicator--nothing about how it factors in to the treatment decision, which is frustrating.  By no means do I want chemo, but even more, I do not want this to come back or flourish somewhere else if it has managed to get out of the breast already.

    Thanks for any additional info.

    Kate

  • Seabee
    Seabee Member Posts: 557
    edited July 2009

    Kate--you can get much information about the Oncotyhpe test, including the basis for their scores, at their website: www.oncotypedx.com

    Look under the Health Professionals tab, where you will find a detailed discussion of the nature of the test.  And yes, Ki-67 is one of the factors included in the score, under the heading of Proliferation.

    Lymphatic invasion strikes me as a little more worrysome than positive sentinel nodes, because it suggests a certain aggressiveness of the tumor, whereas being trapped by a lymph node is a passive process. However, there is no agreement as far as I can see about its prognostic significance..

  • Sydney6
    Sydney6 Member Posts: 172
    edited July 2009

    Kate - I'm interested in the fact that your oncologist said he'd go over the Ocontype with you line by line.  I basically received a graph and a page showing the ER recepyor # and PR receptor #, but no specifics on the individual factors that go into them coming up with a score.  My tumor showed lymphovascular involvement, but my Oncotype score came back as a 12 with an 8% chance of recurrence, so I did not have chemo.  Let me know how you make out.

    Sue

  • orange1
    orange1 Member Posts: 930
    edited July 2009

    LVI is a signifcant predictor of recurrance.  Keep in mind as your read this study that 43% of women in this study had at least one positive node (probably actually more, because lymph node metastasis was not as reliably diagnosed back then) and the average age at diagnosis was 57 years old.  With up to 17 years follow-up some of these women died of old age or other causes.  http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=1356408&blobtype=pdf

    From Ann Surg 2004 Volume 240 No. 2

    Prognostic Value of Lymphangiogenesis and

    Lymphovascular Invasion in Invasive Breast Cancer

    Sebastian F. Schoppmann, MD,† Guenther Bayer, MD,† Klaus Aumayr,† Susanne Taucher, MD,*Silvana Geleff, MD,† Margaretha Rudas, MD,† Ernst Kubista, MD,‡ Hubert Hausmaninger, MD,§Hellmut Samonigg, MD, Michael Gnant, MD,* Raimund Jakesz, MD,* Reinhard Horvat, MD,† and the Austrian Breast and Colorectal Cancer Study Group
  • Seabee
    Seabee Member Posts: 557
    edited July 2009

    Interesting study, Orange. The theory that LVI is a precursor to node involvement doesn't fly, so they aren't very definite on the relationship between LVI and positive nodes. LVI seems most important for what it suggests about thre nature of the tumor, which isn't necessarily the same as what positive nodes might suggest.

    .

  • Kate2z80
    Kate2z80 Member Posts: 66
    edited July 2009

    Orange and Seabee, thanks for the info.  The article was helpful and confirms what I've found as far as LVI being a poor prognostic indicator, particularly in young(er) woman (I am 41).  My lymph nodes (level I, at least) were negative, so I'm going to speak with the oncologist about whether more need be removed.  I suspect not, but I want to be sure.  I just haven't found anything which addresses whether LVI warrants chemo (or at least serious consideration to chemo) where lymph nodes were negative, the tumor was relatively small (mine was 1 cm) and only moderately fast growing (mine was Grade 2).  It just seems like so much is still unknown.  I can't imagine how woman dealt with this years ago, particularly with less access to research.

  • pip57
    pip57 Member Posts: 12,401
    edited July 2009

    A lot of weight is given to the test results of our axillary nodes.  But we do have other nodes that cannot be reached or tested as easily.  Perhaps that is where the concern is.

  • KEW
    KEW Member Posts: 745
    edited July 2009

    More confusing.  My surgical pathology report showed no vascular invasion, however the pathology report from my core biopsy showed "focal vascular invasion."  My onc said it was likely caused by the core biopsy, and not to worry about it.  He said  what mattered was that it didn't show up in the surgical report.  I didn't have chemo based on Oncotype and other factors, but a teeny tiny part of me, in the darkness of night, wonders if the core biopsy may have allowed it to move somewhere else.

    Karen

  • Seabee
    Seabee Member Posts: 557
    edited July 2009

    Kate--There are two answers to that teeny nagging doubt. The first is that a recent event like a biopsy is not likely to release enough abnormal cells to cause a problem. The second is that even if some cells have been released, they are vulnerable to attack by hormonal therapy. Cells that travel probably don't survive very long, which is why so many of them get no further than the sentinel nodes.

  • Kate2z80
    Kate2z80 Member Posts: 66
    edited July 2009

    Karen:

    Interesting.  My biopsy did not note lymphatic invasion, but the surgical pathology did.  I s/w the pathologist yesterday and she said that it was a "small focus" outside of the tumor, so I am going to discuss that with my oncologist when I see him on the 27th.  I did find some encouraging research yesterday which appeared to conclude that only significant lymphatic invasion or lympovascular invasion seems to have a higher mets or recurrence rate.  If true, I can live wiht that.  My (ever growing) file is at home and I will post the link later.  I certainly don't want chemo, but also don't want any regrets later for not hitting this hard enough.

    Kate 

  • homealone
    homealone Member Posts: 38
    edited July 2009

    Hello Kate

    I am in a similiar position to you.Icm tumour,5 negative nodes er+ pr- Her2 pos.My understanding is that the histopathologist reports his findings but the oncologist decides what the treatment will be give certain factors.Each factor of the report will decide what treatment he gives you.In my own case lymphatic invasion is one factor but the greatest factor is the HER2 being positive,so therefore these all indicate chemo.I understand that in some cases looking down the microscope it is impossible to determin whether lymphatic invasion is vascular,as the capillaries are so tiny,or lymphatic so it is reported as vascular invasion.Once this has been identified there is a theoretical chance that some cells could break off and start their travels,they could easily have slipped through a lymph node without node being postive.All these things are theoretical but possible so it is advised to err on the side of caution and give these people chemo.So yes people with lymphatic invasion should receive chemo.

  • LeggyJ
    LeggyJ Member Posts: 726
    edited July 2009

    My sentinel node biopsy, showed one of two nodes, with a speck 1mm tumor.  My surgeon said it was probably knocked loose, during core needle biopsy.  My report, says Lympho-vascular space involvement is identified....I just always thought it was the node.  Like the other have said, I had to do chemo. and rads., to hopefully get anything else out there.  Now I finished with treatment, and taking antiestrogen pills.

    Good Luck 

  • Member_of_the_Club
    Member_of_the_Club Member Posts: 3,646
    edited July 2009

    My understanding is that LVI is not a worse prognostic indicator than positive nodes -- still the most important prognostic factor -- but a kind of an intermediate indicator.  Keep in mind that lymph nodes are used as a kind of surrogate for the bloodstream, through which distant metastasis occurs.  If you have positive nodes you are more likely to have cancer cells in the bloodstream but not necessarily.  And sometimes the cancer goes straight for the bloodstream and avoids the lymph nodes altogether.  I was told that if you have positive nodes, you necessarily have LVI, they go hand in hand.  The grey area is your situation where you have LVI and no positive nodes.  To me this suggests your cancer cells may know how to travel and if you are in the grey area deciding chemo or not, it may push you toward chemo.  But it is only one factor.  It sounds like you have a very thoughtful onc.  Perhaps a second opinion will give you piece of mind.

  • Kate2z80
    Kate2z80 Member Posts: 66
    edited July 2009
    What's "peace of mind"?  I gave that up when I was diagnosed!Wink
  • Seabee
    Seabee Member Posts: 557
    edited July 2009

    If positive nodes and LVI go hand in hand, why is it so often the case that the path report shows one or more positive nodes, but no evidence of LVI? It would seem that they can either coexist or occur independently. As for nodes as prognostic incidators, that's a more complicated business than it may seem, A large tumor that had spent years getting cells to a sentinel node might be easier to deal with than a nasty little aggressive one that went straight to the bloodstream.

  • Member_of_the_Club
    Member_of_the_Club Member Posts: 3,646
    edited July 2009

    Seabee you are right.  If a large tumor has not gotten to the nodes, its probably a slow, lumbering cancer, especially if the woman has known for some time its there and for whatever reason hasn't gotten it checked out.  There are also the large tumors that burst out of nowhere and hit the bloodstream without going to the nodes.  But from everything I've read nodes are the most important indicator.  Not perfect, obviously.

    I was not aware that it could go to the nodes without LVI.  I don't see how that could be, but I believe you.  All I know was that my various docs told me that the fact that I had LVI was not an important factor because I had a positive node, and LVI was part and parcel of that. 

  • lindaps
    lindaps Member Posts: 8
    edited July 2009

    Kate,

    I'd talk with your onc and get his opinion and recommendations but I'd also suggest that after that if you have any nagging fears, that you consider a 2nd opinion.  You have a relatively small window but 2nd opinions are VERY common in oncology.  Unfortuneately I can speak to being on both sides. For years I worked in the medical oncology side as a nurse/ nurse practitioner.  I have subsequently left the onoclogy field and moved into geriatrics and chronic care. I am a 9 year survivor of Hodgkins and have the exact date of diagnosis now with IDC as you.  I had a slightly different scenario than you.  I had a negative sentinel node during surgery and therefore the surgeon moved on to the bilateral mastectomy (1 side BC, other side prophylactic).  However, my final path report showed that I had 2 "micrometasteses" in the sentinel node. ASCO or the American Society of Clinical Oncology meets yearly in May/ June.  There were a lot of discussion on micrometastases but the bottom line is if the met in the lymph node i > 0.2 mm but < 2 mm that qualified as a micromet and was to be considered a + lymph node for BC.  Another oncologist may be able to help clarify the "lymphatic invasion" you identified.  Also there is a free but very helpful telephone number that is sponsored by the National Cancer Institute.

    It is 1-800-4-CANCER. They also have a website which is : http://www.cancer.gov/ where you can do a live on-line chat.  The people who answer or assist you are not physicians but research librarians who search all the most up to date literature to find answers for you.  They'll also help you formulate questions for you to ask you oncologist.  I've used their services personally and professionaly for over 20 years and they are great. I hope this helps.  Please let us know.

    Linda 

  • carcharm
    carcharm Member Posts: 486
    edited July 2009

    I wondered if someone can help me understand this "angiolymphatic invasion." I just got my path report back. Invasive ductal carcinoma 0.3cm moderately differentiated, with multiple foci of microinvasion (less than 0.1 cm each) with ductal carcinoma in situ, grade 3, with comedo necrosis, approximately 1.0 cm in greatest span. Sentinal LN status: negative, i-, Pathologic Staging pT1a N0(i-) Mx. Margins uninvolved by invasive carconma, closest margin 0.6cm.ANGIOLYMPHATIC INVASION (V/L): Present. ER/PR:0 Her2 to follow.

    The er/pr 0 means neagive? The angiolymphatic invasion means??? The blood vessels to the tumor were positive? My lymph nodes showed atypical cells but no malignant cells. No oncotype done yet but with these results it is warranted. I am concerned about the angiolymphatic invasion and the aggresiveness of this tumor. I had a mastectomy with 2 SN. Is chemo warranted in this situation? Also, do I need better margins??

  • Kate2z80
    Kate2z80 Member Posts: 66
    edited July 2009

    Carcharm, I have been struggling with the lymphatic invasion issue, as well, and not found much research on what it means as far as chemo.  I now have my Oncotype report, which does not address the issue.  I did call the pathologist to clarify where she found the invasion and how much there was (thankfully, it is a small focus), but I still don't know what this means as far as adjuvant therapy, if any.  I'm hoping the oncologist can address this more fully when I see him.  I also decided to have a second opinion oncology review and it will include a new examination of the surgical slides by a pathologist.  I am pleased that my insurance will cover this and am going to a major metropolitan facility which treats only breast cancer.  My oncologist is wonderful, but I'm not making any decisions either way without input from at least two (if only for my mental comfort).  I suggest that you avail yourself of this if you are able.  My Oncotype score was 15, which falls in the low recurrence range and, based on that alone, I don't think chemo will be recommended.  However, I need to know how lymphatic invasion factors in and my research did not find much. Thus, two opinions will have to speak to this.  Best of luck.  I was almost hoping for a higher score, where chemo would be a definite, to relieve me of the anxiety of this decision.  How messed up is that?

  • Seabee
    Seabee Member Posts: 557
    edited July 2009

    Member--I was thinking that if tumor cells invade a lympnatic vessel, they will eventually encounter a node, so in that case nodes and lymphatic invasion go hand in hand. But if the lymphatic system picks up shed cancer cells along with other undesirable stuff as part of its normal opreation, active invasion isn't necessary

    We know that cancer spreads, but we don't entirely understand how. It seems probable to me that  it can take more than one route.

  • tibet
    tibet Member Posts: 545
    edited July 2009

    This issue also puzzles me and I still don't understand. In my path, there was no lymphatic vascular invasion in the tumor and there was no vascular invasion but I had 1mm micromet in one sentinal node.

    My doc did tell me if Lymphatic vascular invasion is present in the path that means they can see it, then it means a bit poorer prognosis than those without seen lymathic invasion. What I don't understand is in my case no lymphatic invasion is seen in path but why I had 1mm micromet in one sentinal node? How did that get there? Anyone can help on understanding this?

    Some how the 1mm micromet in one sentinal node bothers me. I like to know if anyone knows the prognosis for micromet in one node is same as node negative?

  • Kate2z80
    Kate2z80 Member Posts: 66
    edited July 2009

    Newalex:

    Wish I could say that I had gained valuable knowledge since my first post, but I have not.  I have had good news, though.  I called the pathologist who interpreted my slides and she also s/w my oncologist.  My oncologist called the head of the pathology department at the hospital, who concurred that there was probably some lymphatic invasion present in my pathology side.  However, my oncologist did not feel that finding, alone, warranted having chemo (I have a lot of positives factored in, including a low Oncotype score [15], negative nodes, ER+, 1cm tumor).  Still, I am having a second opinion, which includes another pathology review.  Although I grilled my oncologist thoroughly today and trust him implicitly, I don't have a real grasp on why the lymphatic invasion isn't of greater concern, so I'd like another oncologist to tell me that I don't need chemo before I can put that nagging concern to rest.

    All I can suggest is push, push, push for answers, further testing and second opinions.  I think alot of the diagnosis and treatment is subjective and there are alot of unanswered questions out there.  I'm not taking any chances, nor should you.

    Kate

  • Pines
    Pines Member Posts: 94
    edited July 2009

    Kate and Carcharm, I am in the same situation.  I am 39 years old.  I was so relieved 0/4 lymph nodes, only then to see my pathology report that said lymphovascular invasion is present ("ectatic lymphatic channels with tumoral nests within their lumens").  My tumor is bigger (1.7cm), grade 2 also, but my original biopsy report showed high ki-67 (proliferation).  My oncologist had not gotten my final pathology report until during my consult with her, so she didn't really go over it, just gave me a copy.  I ordered the oncotype-dx test, but it won't be ready for a couple of weeks.  I don't want chemo and am terrified of neuropathy as well as any possible permanent side effects.  But I don't want to make a poor choice either - I have 5 children (including triplet 5 year olds) that I need to raise.

    Still sitting here with drain tubes coming out both sides of me from bilat. mastect. and am tentatively scheduled for chemo (TC regimen) to begin Aug 13, but waiting to make final decision based upon oncotype-dx score.

    Any comments/advice would be great - I also just needed to share.  Feeling a bit overwhelmed.  Thanks for listening.  It was helpful to read your posts about lymphatic invasion.

    Shay

  • Kate2z80
    Kate2z80 Member Posts: 66
    edited August 2009

    Shay:

    Try not to be discouraged, since all of the facts are not in yet.  The Oncotype test will help make the decision re chemo.  You are stage I and not grade 3, which are both good.  Having the tubes in is miserable and you WILL feel much better when they are out.  I'm surprised that your onco would set you up for chemo without all the info yet.  I am sure that you are overwhelmed, but it sounds like whichever way things go, you have an aggressive oncologist, which is good.  Consider a second opinion whichever way you go.

    Again, try not to freak out.  Waiting is hard, but you will feel more comfortable with the decision (whichever way it goes) once you know more information.

    Hang in there.

    Kate

  • Pines
    Pines Member Posts: 94
    edited August 2009

    Kate, Thank you.  People like you on this site have made all the difference in me making it this far.  - Shay

  • mmm5
    mmm5 Member Posts: 1,470
    edited August 2009

    Shay

    Definitely have the chemo conversation with your ONC and maybe a 2nd opinion. There are many ONC's today that say chemo for over 1cm. Of course your Oncotype will help you make decision but with a high Ki67 and some vasc invasion it may be better to be safe than sorry. My tumor was same size as yours no lymph involvement no vasc invasion and both Onc's I met with stated chemo even if it was not Her2 posititive due to younger age of 42. Chemo is doable and you go away feeling like you did everything. There are several ladies on this board that are stage 1 grade 1-3 that did not do chemo that are scared they made wrong decision. In addition there are lighter chemo regimes these days that don't have as man SE's.

    Good luck you will make the right decision for you.

  • Pines
    Pines Member Posts: 94
    edited August 2009

    mmm5, Thanks for the info.  What chemo regimen did you have?  Are you taking tamoxifen now?

    Shay

  • mmm5
    mmm5 Member Posts: 1,470
    edited August 2009

    Shay

    I did TCH x 6, I am not on Tamox due to some controv. findings with Tamox and Her2. I started with an AI and now am off due to them determining if chemo really put me into menopause.

    Anyway I work in Diagnostics and had access to many opinions when dxed from U of A to UCLA.

    I can't remember but I think you mentioned you were younger and with the VI and being at higher end of stage1 (size) and grade 2 it is something you should atleast dig into for all opinions. By the way I am originally from Oregon what part are you from?

    You can PM me anytime and I am happy to help

  • Kate2z80
    Kate2z80 Member Posts: 66
    edited August 2009

    I just wanted to update my post.  I did get a second opinion, which has helped.  My Oncotype score was 15, but that test does not factor in things like lymphatic or lymphovascular invasion.  My second opinion doctor said I should consider light chemo, but that she would not lose any sleep if I just did the Tamoxifen.  She suggested that I try the light chemo (CMF) and that if I really felt miserable, I could go off and not feel bad about it.  I'm inclined to do it, even though my first oncologist felt it was overtreating.  Either way, I feel much better about things having gotten the second opinion, which included a pathology review.  Incidentally, the second pathology review was more favorable on the invasion issue than the first, which was very comforting information.  This was certainly time well spent and will eliminate the "what ifs" down the road.

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