Update
So. Very upset about upgrade to micro-invasion, and am getting other opinions about that. Talked to the RO, and, interestingly, he is the doc least invested in me getting rads. Said they don't decrease/increase my chance of dying. I was concerned that I have longevity in my family, so had been worried about using my one-time rads chance now, but now get that the years after 70 are not so indicated about rads, and so now am really thinking about the next 15 years being important for that. So; now I feel good about rads. It makes sense, and that's what I, personally, need. He was more concerned that my surgeon and MO were talking about not getting the SNB; he is, after all, first an oncologist. I have to think long and hard about that (lynphedema being 1 in 10). No one here with a micro-invasaion seems to have been told to not get the SNB. Am totally confused about why, with a possible 1-digit chance of recurrence for just DCIS, they were all extremely stressed about me possinby not getting rads, but with a single-digit chance of nodal involvement with the micro, they are saying pass on that. Does NOT make sense.
Comments
-
I had grade 2 stage 0 (dcis) that got upgraded when 1.75 mm of grade 2 idc was detected in my final pathology report from my lumpectomy; that was a big surprise and disappointing to say the least. So instead of going directly right into rads, I had the snb just to make sure that everything was OK (which thankfully it was) and then rads -- no regrets at all, it's been just over 4 years since my diagnosis, glad I did both. I did take a pass on tamoxifen (had a great onc who just laid out all the facts and for me, the costs didn't outweigh the benefits, but these are personal decisions).
These are most definitely your decisions to make. And it is very important to have inner peace; regardless of the future you do not want to play the "what if I had done things differently" game and have regrets.
-
Percy, I'll be honest. When I had my surgery, both surgeons I consulted (at two different facilities) were insistent that I had no choice about the SNB. If my diagnosis had been pure DCIS, they might have agreed to give me a pass (I was having a MX so normally an SNB is done) but with the microinvasion, there was no way that they would have allowed me to go without the SNB.
Here are a few articles about this issue:
From 2011: Role of Axillary Staging in Women Diagnosed With Ductal Carcinoma In Situ With Microinvasion "In summary, this is the second largest series of consecutive patients diagnosed with DCISM. Our data suggest that despite the low likelihood of nodal extension, a
lack of identifiable clinical and pathologic features
associated with a positive sentinel lymph node
precludes the use of selective sentinel lymph node biopsy. Thus, until
further
data are generated and validated, a sentinel lymph
node biopsy should be performed on all patients with DCISM diagnosed
either
on core needle biopsy or after a definitive
resection."From 2005: Sentinel Lymph Node Biopsy in Intraductal Carcinoma of the Breast with Microinvasion "From March
1996 to December 2002, out of 4602 SLNBs performed for invasive
carcinoma of the breast, 41 patients with DCISM in the definitive
diagnosis were selected. Metastasis in the SLN were detected in 4 of 41
(9.7%) patients. Two of the 4 patients had only micrometastasis in the
SLN. In three of these patients, the SLN was the only positive node
after CAD. SLN biopsy should be considered as a standard procedure in
DCISM patients."From 2000: Sentinel lymph node biopsy: is it indicated in patients with high-risk ductal carcinoma-in-situ and ductal carcinoma-in-situ with microinvasion? "RESULTS: ...Of 31 patients with DCISM, 3 (10%) had positive sentinel nodes. 2 of 3 were positive for micrometastases only.... CONCLUSIONS:This study documents a high incidence of lymph node micrometastases as
detected by sentinel node biopsy in patients with high-risk DCIS and
DCISM. Although the biological significance of breast cancer
micrometastases remains unclear at this time, these findings suggest
that sentinel node biopsy should be considered in patients with
high-risk DCIS and DCISM."I also reviewed the NCCN Treatment Guidelines (physician's version 1.2014) to see if there was any mention made of possibly being able to pass on having an SNB when the diagnosis is DCIS-Mi. DCIS-Mi is grouped in with other Stage I cancers, and no exceptions to the SNB requirement were noted. Within the DCIS section, the following was noted: "Patients found to have invasive disease at total mastectomy or
re-excision should be managed as stage l or stage ll
disease, including lymph node staging." NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines)® Breast Cancer Note that you need to register on the NCCN site (it's free) in order to be able to access the physician's guides. Patient Guides are available without registering but they don't provide the same amount of detail. -
Thanks for all that. After another Kaiser path report, and Dr. Lagios, I SHOULD know if I actually DO have a micro-invasion. I've seen women here who were told they did, and sent it on to a bigger or different hospital, and were told it was not, in fact, a micro-invasion. This is all crazy-making. My surgeon said it was called that because it was outside the milk duct. From what I've read here, that's not true. It could be outside the duct from the biopsy, but still be just DCIS. To be a micro-invasion, it's about it being pathologically different, not just that it's outside the duct, right? The Hr2 (or whatever it's called) assessment on the micro is pending. Can that test even be done on DCIS, or would the ability for that tissue to be able to have that test successfully completed prove it's a micro-invasion? Why don't these people always seem to know what they're talking about, and why am I having to do their work for them? As I said, I am astounded that two smart docs, a breast surgeon and an MO, were frenetic about me having rads for a tiny bit of just DCIS, but are casually telling me it's safe to not do the node.
-
Percy,
DCIS can only be outside the duct if it was placed there accidently - by a surgical instrument, for example. It's been known to happen.
IDC cells are different biologically from DCIS cells, but this difference can be very difficult to detect. Here is an interesting presentation that talks to this issue: Problems in the Diagnosis of Ductal Carcinoma in Situ See pages 33 to 55. Additional immunostains for myoepithelial cells may be done to try to determine if the cells are DCIS or IDC but my understanding is that this doesn't always provide the answer. See the discussion of In Situ v. Microinvasion near the bottom of this web page: Immunohistochemistry in Breast Pathology
As for HER2 testing, yes, this can be done on DCIS. So the fact that the microinvasion will be tested for HER status doesn't tell you that this truly is a microinvasion, vs. it being DCIS. As an FYI, approx. 40% (some studies have suggested higher) of DCIS is HER2+, whereas only 20% - 25% of invasive cancer is HER2+. No one knows why this is. And while HER2+ DCIS has been evaluated in many studies, most of the studies show there to be no difference between HER2+ DCIS and HER2- DCIS. A few studies do show HER2+ DCIS to be more aggressive, but there have also been one or two studies that have shown HER2+ DCIS to be less aggressive. With IDC, it is well established that HER2+ IDC is more aggressive. So the reason that DCIS often isn't tested for HER2 status is not because it can't be done, but is because there is no known significance to HER2 status for DCIS. There also is no difference in treatment between HER2+ and HER2- DCIS.
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