Lack of emphasis on vascular invasion
Comments
-
Its so strange how one Onc says one thing and another says different thing. My Onc even stressed that I strongly think about chemo since I had extensive LIV and the 3 nodes they took out had mets in them. I am still confused at the whole deal and I have finished treatment.
-
Isabelle4, Aren't people supposd to live happily ever after in fairy tales?
-
i was node-positive, Grade 3 and LVI. I thought I was doomed, but my ONC just insisted that these factors made chemo a great treatment for me. I opted for a BMX and still ended up with rads too. Now I take Tamoxifen and will switch to an AI in 5 years. So . . . I've pretty much thrown the kitchen sink at this crap. Strangely enough my ONC never mentioned LVI. I read about it on the pathology report. The positive nodes were what dictated the aggressive treatment plan.
-
I think sundermom has it right. Unfortunately for some of my Stage 1 friends who thought all was clear, they had recurrences. And, I've got young women friends in later stages who have stayed disease free for much longer than expected. I think the Oncotype has been an incredible window into the nuances that take place within the categories--grade 3 isn't always high recurrence, for instance. Mine wasn't. And so, these bucket categories...the doctors realize the staging nomenclature is getting outmoded quickly.
-
LtotheK, So true, that not all Grade 3's are equal or behave the same way. I have also heard the higher Stages, with their more aggressive treatments, sometimes fare better than an earlier Stage that hasn't been treated as aggressively.
Whether your path. report says "LVI" or not, if you have positive nodes, your lymph system has been invaded; therefore, if the path report say something like 2/5 nodes positive, it is not really necessary to also include the phrase LVI. However, there could be instances where the nodes check out clear, but LVI is detected in the tumor sample under the microscope. Then what? That's a gray area.
-
elimar. I have 'extensive vascular invasion' BUT 26/26 nodes were clear. ( or so I was told )
Isabella.
-
LVI was on my path report and it really freaked me out. My MO never mentioned it at all and when I asked the RO he didn't seem that concerned about it. He was more concerned about the positive nodes and I also had extracapsular extension. I just hope that all the chemo I had and then radiation took care of it all.
-
Isabella4, What treatment did you get? Chemo or no chemo? You are over 8 years out, so whatever they did got you this far.
-
elimar... BMX, 20 rads, plus Arimidex (still on it )
-
Like Weety,
the biopsy revealed a LVI- angiolymphatic (sp?)
But the Surgery pathology reported: LVI= not present
Which should we go by? and Why might the biopsy differ from the surgery pathology?
Anyone have any experience or answers to that?
-
withlove,
I have asked EVERY doctor I've seen about the biopsy showing LVI and I could never really get a satisfying answer. From what I was told though, was that probably the LVI was very tiny and it is even possible that the only area of LVI was in the exact place that it was biopsied. Another onc explained it to me that when they check tissue removed they can't check every little area. They slice it and do "samplings." A "sampling" they checked at biopsy had LVI, the "samplings" they checked after mastectomy did not. He said that's a good thing because it means the LVI was minimal. My first onc said that she suspects that many, many more women have LVI than is found and reported because of this same thing--if it is minimal, the sampling might miss it. All doctors said, though, that I have to go by the biopsy findings--if LVI was seen, it was there. That is something that is real--someone looked through a microscope and saw it. I guess we have to take a little relief in that it must have been minimal.
Anyone else know anymore about this?
-
I did some research on this topic, as I had that very weird biopsy showing LVI and final pathology didn't. I can say that my oncologist was not particularly impressed with the LVI status in the biopsy, and said we really needed to wait for the final surgery (so it was kind of the inversion of weety's experience). The research I did indicated the biopsy can cause disrupted tissue, so the samples are not always accurate.
It's just another one of many, many elements of my treatment for early stage BC that has haunted me, and finally made me realize we just don't have that much control in the matter. I did 4 TC, that's as good as one could do with LVI anyway.
-
This study has floated around quite a bit on these boards, it is an excellent one: http://jnci.oxfordjournals.org/content/101/10/729.full
Basically, the findings are, if you are high risk for recurrence, the LVI seems to have independent prognostic factors. If at low risk, it is not an independent prognostic factor for recurrence.
Generally speaking, this is so totally out of our control that it's probably best to know what we know (which is more than so many patients), and go have a nice day. Yeah, it freaks me...
-
Weety and LtotheK, seems like both of you can be "right" about what's going on. If LVI is seen, then it's seen, so if it appears on biopsy or FPx you have to assume that you, indeed, had some LVI. In the case that it could be "rearranged" somehow by the biopsy (or the surgery for that matter) you would still need to err on the side of caution and proceed like it was legitimately present as far as treatment goes.
Anyway, although the OP has not come back, in her other postings she mentions having 3 positive nodes and doing chemo, so moot point for her. I mean if you have pos. nodes, you have lymphatic invasion, don't you?
The question of having clear nodes, yet showing LVI on any pathology is still an interesting topic that we have not heard all that much about.
-
The question of having clear nodes, yet showing LVI on any pathology is still an interesting topic that we have not heard all that much about.
Elimar, the study I posted addresses that point exactly. It appears if one does not have other risk factors, the LVI is not a stand-alone risk factor. Now, in my case, I'm all over the place. Grade 3, low oncotype, fairly young at diagnosis, but not too young according to what was considered an additional risk factor.
It's interesting to me how many of us really fall in a huge grey zone. So very hard to know what to do. In any case, after reviewing this thread, and hearing multiple opinions, I'm very glad I opted for chemo. My case is really wiggly.
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team