"Lymphovascular invasion is not identified"

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Hester32
Hester32 Member Posts: 3

Just got first report after biopsy. Breast surgeon made appt. for two weeks hence, April 5th. Long time to wait - already 3 weeks since "suspicious assymetry" was seen on routine mammo.

Report says "infiltrating carcinoma with features of micropapillary carcinoma". Looked that up - it's a rare and very aggressive form, with very high risk of spread to lymph system. Report also says "Lymphovascular invasion is not identified". Apart from size (5mm) they didnt give any more info - like grade or stage - it says "prognostic test results pending". .

Key question: what's "not identified" mean. That the biopsy sample didn't include any lymph nodes, so they couldn't identify if mine are cancerous? Or that they did test one/some nodes, and they did not identify any cancerous cells? Only 4 cores were sent - that doesn't sound like a lymph sample was included?


Comments

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

    Core needle biopsy does not test lymph nodes, that would be done with a sentinel node biopsy (SNB) during whatever type of surgery you end up having. The notation regarding lymphvaacular invasion is looking at whether this is present, or not present, in your core samples, "not identified" means you don't have it. Lymphvascular invasion occurs when cancer cells have broken into the vascular and lymphatic channels in the breast tissue. While it is certainly is better not to have LVI, its presence or absence is not reliably prognostic. Grade is part of what is pending in your biopsy pathology report, along with what your hormonal receptors and Her2 status is, and will partially indicate level of aggressiveness of the cancer.Stage is determined after surgery when the tumor is analyzed for size, final path report on hormonal receptors and Her2, and nodal status after SNB. Hope this is helpful, wishing you the best.

  • Scwilly
    Scwilly Member Posts: 489
    edited March 2016

    Pathology reports can be confusing. When I first got mine ( first one from biopsy, second from first UMX, third from Second UMx) I read through each one but not in detail. Later I took them line by line to see what they said. My biopsy had lymphovascular invasion: identified. Afer chemo the path report said 'Lymphovascular Invasion: not identified' my third path report showed DCIS, so did not report Lymphovascular invasion. On research, I discovered this meant (in simple terms) this was about the presence or not of cancer in the breast tissue and vessels on the way to the lymph nodes.

    See the Wiki page: https://en.m.wikipedia.org/wiki/Lymphovascular_invasion

    Or the info on this site: http://www.breastcancer.org/symptoms/diagnosis/vasc_lymph_inv

    So it could be thought that it's a good thing to have 'not identified'. For breast cancer the Wikipedia page says "In breast cancer, LVI is not an independent risk factor for a poorer prognosis."

    I hope this helps.

    Best wishes

    Sarah


  • Hopeful82014
    Hopeful82014 Member Posts: 3,480
    edited March 2016

    Actually, nodes are sometimes sampled by biopsy if there is reason to suspect involvement at time of diagnosis. My ultrasound showed enlarged nodes which were sampled and found to be malignant. I don't recall, however, whether the nodes were sampled by FNA or core biopsy, as opposed to the tumor which was definitely core biopsy.


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

    hopeful - I didn't mean to imply that nodes are not sampled at the time of biopsy - my error, just that the OP would have most likely known axillary nodes had been sampled in addition to the breast mass, and that the core biopsy of the breast does not give indications regarding nodal status in the axilla. Thank you for clarifying that sometimes suspicious nodes are looked at during biopsy.

  • Hopeful82014
    Hopeful82014 Member Posts: 3,480
    edited March 2016

    Thanks for clarifying that, SK. I appreciate it and hope the OP found it helpful, too.

  • Hester32
    Hester32 Member Posts: 3
    edited March 2016

    Thanks all. Doctor daughter of a friend thinks it means no cancer cells found in the lymph vessels that are part of the regular biopsy core. Good sign, but doesn't prove that lymph nodes are clear. Guess I'll need a sentinel node biopsy, will ask to have it done at same time as lumpectomy. Wish to heck doc would see me sooner - dunno if she's waiting for follow-up tests ("reflex to HERMARK" was written in clinical data box on the biopsy report - does that mean the HERMARK test was requested? Hope so). But maybe doc is just busy (breast cancer surgery dept at large hospital) .

    Couldn't be more irritating to have a 14 day wait from diagnosis to seeing the doc on April 5th. Is that a normal wait, after biopsy lab has told GP that the report is "urgent". I'm due to leave April 9th for a 3-week overseas vacation! To pack or not to pack... difficult to do packing and preparations for a three weeks absence in three days!

    Found item on WHO Guidelines from 2012 saying they decided micropapillary form is not necessarily a worse prognosis after all. Unless the microcalcifications have a "tram track" pattern. I know there are scattered microcalcifications, previous mammos have mentioned, but nothing said so far about any microcalcifications in the tumor area.

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

    hester - yes, that is what the above posts indicated - no cancer found in the tissue or vessels of the breast - in the core samples submitted, but this has no direct bearing on whether there is cancer in the lymph nodes themselves. Sentinel node biopsy (SNB) is routinely done at the time of surgery, and the vast majority have SNB done simultaneously with breast surgery. A few have it done the day before, but that is their facility policy, and is not as common. Reflex to HERmark means that if your initial Her status testing is equivocal (not positive and not negative, as sometimes happens) then Hermark testing is requested - this is the reference to "reflex" - that is done when an additional test needs confirmation. I don't know if this means this is what is being requested IF you get an equivocal response, or you have gotten one and now the reflex testing is being done with that particular testing modality.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2016

    I have read this thread and am confused. Does cancer not have to cross over the breast tissue through the vascular tissue to get to the lymph nodes? If not then how does it get to the lymph nodes and NOT be in the vascular tissue of the breast? This is such a confusing topic.

  • BarredOwl
    BarredOwl Member Posts: 2,433
    edited May 2016

    Dollydimples123:

    The circulatory system includes two types of channels or vessels for fluids: (1) the "vascular" system for blood; and (2) the "lymphatic" system for lymph fluid.

    The breast has small blood vessels and lymph vessels going through it. Either system may be used by tumor cells to escape the breast.

    If they have the capability to do so, cancer cells may break into a nearby lymph channel in the breast and travel through the lymph system to regional lymph nodes.

    Cancer cells may also break into a local blood vessel and travel elsewhere via the bloodstream.

    The pathologist looks at the lymph vessels and the blood vessels in the vicinity of the tumor for signs of lymphatic invasion (breaking into a lymph vessel) or vascular invasion (breaking into a blood vessel). If they don't see signs of either of these in the sample, they may note "lymphovascular invasion" ("LVI") is not identified.

    BarredOwl

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2016

    BarredOwl,

    Thank you so much for that very clear explanation. Helps me a lot. So can I ask then, would this come up during the biopsy pathology report or the pathology report AFTER surgery?

    I am confused as when I was diagnosed a few weeks back, I was told that it had not gone into lymph nodes and was not invading any breast tissue. I am not sure how they would be able to say this when all they had was mammo, biopsy and U/S results. Maybe I am wrong?

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

    LVI can be present in either biopsy samples and full tumor or breast tissue pathology samples - it was noted in both my biopsy pathology report and pathology report after BMX.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2016

    SpecialK,

    Thanks for this. I did not realize that the initial biopsy could tell them so much. I still have not been staged yet, as he would not commit to that til lumpectomy was done. But I am assuming that they sort of know a fair bit after they have gone and and looked at nodes and breast. My BS took out only 2 or 3 nodes during op and didn't even use the blue dye...(not sure why).

  • BarredOwl
    BarredOwl Member Posts: 2,433
    edited May 2016

    Dollydimples123:

    Elsewhere you said you have invasive breast cancer. By definition, the tissue of the breast (stroma) has been invaded. Invasive disease (where cells have broken through the wall of the ducts or lobules into surrounding breast tissue) can occur without any lymphovascular invasion ("LVI").

    Prior to your surgery, perhaps the absence of clinically suspicious nodes (no enlargement on clinical exam); the absence of evidence of LVI on breast biopsy (assuming vessels were seen in the biopsy sample); and normal imaging findings (regional lymph nodes seen were normal in appearance) means there was no basis to be suspicious of lymph node involvement. These are favorable findings, but are not conclusive and do not exclude the possibility of lymph node involvement. That is why a sentinel node biopsy was done.

    They can use a radiotracer to find the sentinel node(s).

    When your results are in, be sure to request complete copies of the pathology reports from all biopsies and surgeries, including any supplements or addenda thereto (e.g., containing ER, PR or HER2 testing) and review these yourself. Trust, but verify.

    BarredOwl

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2016

    Thanks BarredOwl,

    Yes I was told on my first appointment that I had invasive breast cancer. I think that is what has confused me with all of this. If invasive means that it has the potential to invade vessels etc but that it may not have done, then I can understand that a bit better. I do get however that the biopsy is THE final test to tell me what is really going on. I was also told it was ER+ and PR+ and HER2-. The surgeon seemed very positive overall and very unexcited by my case as in ...why was I worried to death as this was early and caught before they could even feel a lump! They have no idea how I even managed to find this! The RO said I needed congratulated on finding it! So I suspect someone more powerful than me is guiding me at this time!!

    I shall most certainly make sure to ask for all lab results on Monday. In the meantime I am eating organic in every single thing. Cupboards were cleared of all foodstuffs the other week and I have joined the gym and getting out everyday for some form of exercise. Have also started yoga classes. My main aim is to lose weight, get healthy and de-stress. I am convinced stress is at the root of this for me.

    It is very helpful to have people like you who seem to be very knowledgeable about this as I get my head pretty confused by all the letters and tests and and numbers attached to everything. I think you need a PhD to be able to understand this subject!!

  • BarredOwl
    BarredOwl Member Posts: 2,433
    edited May 2016

    Hi Dollydimples123:

    It is hard to understand, particularly at first, when you have to learn so quickly and you are stressed (which did not aid comprehension for me).

    Sometimes, with IDC where the tumor is greater than 0.5 cm in size, and ER+ PR+ HER2-, no LVI, and negative nodes (N0), chemotherapy may still be considered or recommended. This is because even sentinel node biopsy is not a perfect method, and there can still be some risk of undetected distant spread.

    Tests such as the OncotypeDX test for invasive disease (for hormone receptor-positive, HER2-negative disease) or MammaPrint (more common in Europe) are sometimes used to obtain more information about estimated recurrence risk and help inform decision-making regarding whether to add chemotherapy to endocrine therapy (e.g., tamoxifen or an aromatase inhibitor) or not. Hopefully, you will have the opportunity to meet with a medical oncologist to discuss possible testing and options thoroughly prior to any further treatment.

    Hoping for the best possible pathology results for you!

    BarredOwl

  • pupmom
    pupmom Member Posts: 5,068
    edited May 2016

    I just want to mention that it is very helpful if people would fill in the diagnosis section. Others cannot respond intelligently without that info!

  • BarredOwl
    BarredOwl Member Posts: 2,433
    edited May 2016

    As far as Dollydimples123 goes, she is still awaiting the results of surgical pathology and SNB. She has indicated her receptor statuses above (presumably based on biopsy) as "ER+ and PR+ and HER2-." I happen to know from another one of her posts that based on biopsy and imaging, she was diagnosed with an estimated " 1.1cm x 1.5cm and grade 2 invasive cancer".

    BarredOwl

  • pupmom
    pupmom Member Posts: 5,068
    edited May 2016

    Thanks Barred Owl. I have noticed over the years that many BCO participants neglect or choose not to list their diagnoses, so it is easy to find. The very first thing I did was fill in this section. I just don't understanding why those who know their stats, not Dolly right now, don't do this. I understand privacy issues, however. So I probably shouldn't ask, except when people request advice it is a real deterrant, in terms of being helpful.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2016

    Hi Yorkiemom,

    BarredOwl is right in that I have no details to list at the moment as I am awaiting my results.I will update as soon as I have these detais in.

    I got a call from my BC nurse today to tell me that I was to go see the oncology department on Thursday about possibility of having chemo. However there are no results through even yet on my actual biopsy or SNB. My next question of course was how can you be thinking about chemo if you have not had results through...was told that it would just be good to see the doctor and find out and ask questions about this particular treatment. I got a vague feeling something was not right. Not sure if nurse had made some sort of mistake or was not too well versed on my details etc...seems strange to send me to a dept to speak about a treatment that I have not officially been told I am having yet. But maybe that is common procedure?

    I was initially told I would most likely be getting lumpectomy, radiotherapy and Tamoxifen. When I asked about chemo last week, my BS said he didn't know for sure til op was done and result in from that. So this call was a little distressing and upsetting. Not because I am worried about having chemo, just that this was a shock I had not been prepared for fully.


  • pupmom
    pupmom Member Posts: 5,068
    edited May 2016

    Dolly, I totally understand why you can't provide that info! For me, the biopsy confirmed it was invasive, but low grade. However, nobody thought I had nodes involved, until the big shocker during surgery. Yet I still dodged the chemo bullet with a low Oncotype score. The Oncotype report actually said I was more likely to die from chemo than cancer!

  • Angtee15
    Angtee15 Member Posts: 209
    edited June 2016

    I have a related question: my final path report post BMX says "not observed" for both vascular and lymphatic invasion. I don't see the Oncologist until Monday but I am wondering if it means they didn't see it (yay), OR they didn't test for it. I had a SNB that was clear before starting neoadjuvant chemo so maybe my samples weren't tested for LVI? I hope that is not the case since I still had 25% of my tumor left at surgery and who knows what that #$% was up to these past six months.

  • BarredOwl
    BarredOwl Member Posts: 2,433
    edited June 2016

    Hi Angtee15:

    LVI is a phenomenon that is separately assessed regardless of whether an SNB is performed or not. My understanding is the pathologist looks at the lymph vessels and the blood vessels in the vicinity of tumor cells for signs of lymphatic invasion (breaking into a lymph vessel) or vascular invasion (breaking into a blood vessel). If they don't see signs of either of these in the sample, they note "lymphovascular invasion" ("LVI") is "not identified" or "not observed". These phrases mean they did look for it, but didn't see signs of it.

    I am a layperson with no medical training, so please confirm this when you meet with your MO on Monday.

    BarredOwl

  • Angtee15
    Angtee15 Member Posts: 209
    edited June 2016

    Thanks Barred Owl

  • jbdayton
    jbdayton Member Posts: 700
    edited June 2016

    Another note, you may be assigned an oncologist even if you don't have to have chemo. The oncologist many times is the doctor who will prescribe and monitor your Tamoxifen Or AI drugs. Just go with an open mind to this appointment. Good luck. Sending positive thoughts

  • HelenWNZ
    HelenWNZ Member Posts: 485
    edited June 2016

    I got my pathology results back today and am now am freaked out more.

    35mm grade 2 IDC with prominent micropapillary component present.

    Extensive Peritumoral lymphovascular invasion seen admixed intermediate grade DCIS present

    ER8 PR6 HER2+

    Resection margins 6mm from inferior >10mm all other margins

    Extensive axillary disease present 18/22 nodes with extensive extra nodal spread evident.

    All gross macroscopic disease was excised from axils at the of surgery.

    Now on to chemo, herceptin plus radiotherapy and hormonal therapy.

    Doesn't look good for this 52 year old body who had a clear mammography 21 August last year.

    Anyone have any words of wisdom.


    Thanks


  • BarredOwl
    BarredOwl Member Posts: 2,433
    edited June 2016

    Hi HelenWNZ:

    Please confirm it with your team, but my layperson's understanding is that the lymph node status and involvement is a more important finding than the LVI, both with respect to prognosis and treatment decisions. Under our local NCCN guidelines, the main considerations for selection of systemic treatments (chemotherapy, HER2-targeted therapy, and/or endocrine therapy) for invasive breast cancer are histology (e.g., ductal, lobular, etc.), lymph node status, tumor size, hormone-receptor status, and HER2 status. Factors such as LVI, grade, Ki-67 (if measured), etcetera may be considered in closer cases.

    DCIS or "ductal carcinoma in situ" is often found in association with IDC. In contrast to IDC, DCIS is a "noninvasive" disease that is confined to the inside of the ducts (has not broken through the walls of the duct), and so DCIS does not pose a risk of distant spread. If the mastectomy margins with respect to both the DCIS and IDC are 6 mm from inferior and >10 mm all other margins (please confirm it with your team), then the mastectomy appears to have adequately addressed the DCIS component, and the features of the IDC will determine treatment along the lines you have noted.

    I would recommend that you join the "Triple-positive Group" thread, but I see you have already found them. :)

    https://community.breastcancer.org/forum/80/topics/764183?page=1000

    I have no words of wisdom, but send you my best wishes as you move forward with treatment.

    BarredOwl

  • HelenWNZ
    HelenWNZ Member Posts: 485
    edited June 2016

    Thank you BarredOwl I google too much which makes things even bleaker. The report I got wasn't great To look at in black and white.

    I guess this is where we put our trust in the professionals and try not to get too phased out.

    Another online friend has told me that this is a marathon and we are in in for the long haul.

    Take care

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