DCIS with microinvasion?
Comments
-
Just posted this question in the thread about my mom's treatment but thought I would get more response as a seprate topic.
I just found out she has microinvasion - still waiting to get a copy of that report in my hands. What does this mean? I've read a bit but not getting all the answers. How much more serious is this? Does this dramatically change treatment options?
-
onkell, I had a microinvasion along with extensive high grade DCIS. About 10% - 20% of women who have DCIS have microinvasions.
In most cases, there's only one change to the treatment plan caused by the microinvasion. Many women who have DCIS, particularly if they have a lumpectomy, don't have their lymph nodes checked. But once a microinvasion has been found, it's important to check the nodes. The likelihood of having lymph node invasion from a microinvasion is small - only about 10% - but it needs to be checked out. So if your mother hasn't had a sentinel node biopsy (SNB), then that probably will be done at the time of her next surgery.
Other than that, assuming that there is no invasion into the lymph nodes, the microinvasion should have no effect on her treatment plan. After a lumpectomy for DCIS, your mother probably would require radiation regardless of whether or not the microinvasion is there. If your mother's BC is ER+, Tamoxifen will probably be discussed as part of the treatment plan, whether or not the microinvasion is there. Chemo is never required for pure DCIS and is rarely discussed for invasive tumors that are less than 5mm in size, so having a microinvasion should not add chemo into the treatment plan.
The only other change resulting from the microinvasion is that your mother's cancer is no longer DCIS Stage 0. With a microinvasion, she moves up to Stage 1 (T1mic). With that comes a very small future risk of distant recurrence. Since DCIS is non-invasive, distance recurrence (i.e. outside of the breast) is technically not possible because the cancer cells were all removed while they were completely contained within the milk ducts of the breast. However with any amount of invasive cancer, even the tiniest amount, there is a very slight risk that a cancer cell might have escaped out of the breast prior to the surgery. So distant recurrence is a possibility, although the risk is very small (maybe 1%?) and a drug like Tamoxifen would be effective at reducing this risk even further. It's not something that's likely to happen, it's not something to worry about, but it is something to be aware of.
Hope that helps.
-
Bessie, very helpful. thank you!
So I just got her report and trying to make sense of it.
It says pathologic stage: pT1mic, pNx, pMx
You answered my first part, what are the other two?
-
onkell,
Staging is based on 3 factors:
- T for tumor
- N for nodes
- M for metastisis
In your mother's case, the tumor is T1mic, which as you know means that she has a microinvasion of IDC.
The pNx means that the nodes can't be assessed - probably because none have been surgically removed yet. Once your mother's nodes are checked, this will be changed. Hopefully the result will be pN0, meaning no cancer found in the nodes.
The pMx means that there is no assessment of metastases. This is unlikely to change since most often for women who have DCIS or very early stage 1 BC, although blood tests and chest xrays may be done, additional body scans (CT scan, bone scan) to check for mets are not considered necessary. If your mother's nodes are clear, the pMx might be left as is and your mother would still be considered Stage 1 even with the gap in information. The pM0 (no metastisis) would be assumed.
-
Beesie, THANK YOU. I learn from your posts all the time. My path report reads: pTis Nx Mx. Now I understand what that means. I'm sure the "pTis" is "in situ" or stage 0 (which it was).
Mary D.
-
Mary,
Yup, the "is" in pTis means "in situ". In your case, because you had DCIS, you didn't have your nodes checked or any body scans to check for mets. So you are Stage 0 with the assumption of no node involvement (Nx) and the assumption of no mets (Mx). Although Stage 0 is usually listed as pTis, pN0, pM0, in fact most DCIS women don't have those other tests so your designation is probably more common.
Cheers!
-
Bravo......our DCIS 101 class.......thanks Beesie.
I spent hours looking that stuff up!
-
Beesie,
My situation is a little different, and I am hoping you can provide some of your expertise -- while I climb the walls waiting for my doctor's office to re-open after the holiday.
After a stereotactic biopsy, I was diagnosed with DCIS. I had a double mastectomy 7/25/13 with no sentinel node biopsy. On 8/8/13, I followed up with my surgeon who said my pathology report came back all clear and I was good to go. I was in his office on 11/26 (for another matter) and asked for a copy of the pathology report and found that 3 days after we met the path report had been amended. When staging the cancer, the found a micro-invasion.
So, here we are 4 months later, BMX is completed as is TRAM reconstruction. What can be done to know if the cancer spread?
Amended Path Results: DCIS, High Nuclear Grade in Upper Outer Quadrant, focus of microinvasion is identified, no DCIS at margins. And, then there is this note which makes me hopeful that maybe it's not as bad as I am fearing: The focus of micro-invasion is only identified in the additional level cut for the receptor status evaluation.
Thoughts? Thanks in advance. I am new to this board and have received quite an education reading your posts!
KLB -
Klb3141. The initial posting was back in 2008 and Beesie may not have this thread still in her favourite topics. I'd recommend sending her a private message to ensure you gain her attention. She truly is wonderful with her knowledge and her ability to share it so the rest of us can understand it. -
Thank you, Linda. I have followed you're advice -
Klb,
I got your PM but I will answer here so that others have a chance to read this and offer their input too.
Have you talked to your surgeon about this? I'm really not sure what to suggest.... normally an SNB is done at the time of a MX for women having a MX for DCIS, if there is thought to be any risk that invasive cancer might be found hidden with the DCIS. However your risk of nodal involvement is probably extremely small with such a tiny microinvasion - do you have the size dimensions on it? Typically a microinvasion is 1mm in size or slightly smaller; it sounds as though yours might be quite a bit smaller than that and that would of course considerably reduce the risk of nodal involvement (which is about 10% with a 1mm microinvasion).
Here is a more recent thread written by someone who had the same issue:Topic: What is next for IDC mastectomy with no sentinal node biopsy.
You might want to follow with this individual to see what she and her doctor decided to do about the situation.
Sorry I can be more helpful on this! -
Bessie,
Thank you for your dedication to education and support. You're posts are amazing!
I haven't spoke to my doctor yet as I just read the amended report lastnight and today is Thanksgiving in the good ole US of A. I am not sure if is office will be open tomorrow but I will be calling! And, I have already sent two emails to his coordinator. Waiting is difficult -- I haven't even told my husband about. Beesie, you and Linda1966 are literally the first to know.
So, hopefully this is the information you're looking for:
Amended Final Anatomic Staging- Pt1mi Tumor less than or equal to 1 mm in greatest dimension
- pN0 No regional lymph node metastasis histologically (i.e., non greater than 0.2 mm), no examination for isolatated tumor cells (ITC)
Other noteworthy statements in the report:- The focus of microinvasion is only identified in the additional level cut for the receptor status evaluation.
- Within the soft tissue closest to the suture denoting the location of the axilla there is a single possible lymph node measuring 1.5 cm in greatest dimension. (My interpretation is that while there may have been 1 lymph node in the tissue, it probably would have been a miracle if that was the sentinel node).
I will follow up on the other post. This one is a head scratcher... I wouldn't want to remove all those lymph nodes without certainty of getting the 'right' one. I guess I was hoping something like an MRI or PET scan could get the job done.
I am guessing hormone therapy is a possible change in my treatment. I have two separate scores for ER: 2+ 51% of microinvasive carcinoma and 3+ positive in >90% of DCIS. I don't like the idea of a rogue High Grade cell running rogue, but at least I am ER+...
Time to hurry up and wait!
Thanks again!
klb -
Klb3141, can't remember if you had a lumpectomy or mastectomy. Anyway, many surgeons now are choosing not to do ALND, but using radiation to mop things up. Maybe this is a possibility for you. -
I had a double mastectomy. I really hope ALND is not part of the discussion... : ) -
You could still get radiation, but might have to go through it for several weeks. But maybe you don't need anything! -
Klb,
Now I'm really confused. I don't see how the pathology report can state "pN0 No regional lymph node metastasis histologically (i.e., non greater than 0.2 mm), no examination for isolatated tumor cells (ITC)" if you did not have a sentinel node biopsy involving the removal and pathological analysis of regional lymph nodes.
"pN0" means that pathologically there is no evidence of invasion - the "p" is used in front of the "N0" only when referring to a pathological sample. Also the fact that the word "histologically" was used indicates that this was an examination under a microscope. The fact that the single lymph node was found within the breast tissue doesn't seem to explain this since the report states "there is a single possible lymph node measuring 1.5 cm in greatest dimension" - and that certainly doesn't sound as though it was this lymph node that was analysed and found to have no evidence of invasion. If it was, the report should stating and that and it likely wouldn't say that it was a "possible lymph node".
More questions for your surgeon. -
Maybe he did one without me knowing it. That would be wonderful. But the wording 'possible' really throws me off on this report. I would think if this node (or possible node) was the sentinel node it would be a clearly marked specimen and clear in the report. No doubt -- me playing amatuer doctor is probably a very bad idea. I will hopefully find our more on Monday. Office is also closed tomorrow...thanks for looking at all of this and weighing in. I so appreciate it. -
aklb- wondering if you recall if you signed consent for a sentinel node bx? Its possible they did it with methelyne blue dye while you were under anesthesia versus a nuclear med injection before you went in. If you were having a planned sentinel node bx there would be separately labeled specimens for each node (typically 1-3)
Reading this it appears that the micro invasion is in the section of the specimen that they did the er/pr/her2neu on. In my case that specimen was not from my surgery- it was from the core bx
Secondly- you had a mastectomy which is a large amount of tissue removed and they usually will mark with suture and label each area
- what this is saying to me is that there is a part of the specimen that includes a possible lymph node in it. My sense is this was not taken out necessarily "on purpose" but part of the overall dissection of the breast tissue during your surgery and it came along with it.
I am not sure why you are thinking you need an entire axillary node dissection- did they say that to you? Sentinel node bx can be done with fewer nodes removed based on where the contrast (nuclear medicine or dye) goes first. -
I don't recall discussing a sentinel node biopsy or signing a consent. I really think i would remember that. But I am glad to know there is a possibility they used dye while I was under. Barring that, I believe you are right that the 'possible lymph node' just came with the rest of the tissue. That is my theory as well. And, you are right the microinvasion was found only in the sample used for hormone receptor testing (and it was taken during the mastectomy). My original path report was noninvasive. The amendment came later with the hormone receptor testing. Unfortunately, my follow up appointment was before the amended report came in. My doctor gave me an all clear and never informed me of the change in the report. I only found out when I requested a copy of my path report 'for the files' earlier this week (and read it last night). That's why it is four months later that I am learning of the microinvasion.
I haven't hady any conversations with the docs yet due to the holiday. My entire question is what tools exist to confirm no rogue cells made it into the lymph nodes now that I am four months passed my mastectomies. I don't know how a sentinel node biopsy can be done when the tissue was removed four months ago. I read the links about post mastectomy sentinel node biopsy but it seems like that was only an option for a short time period following the mastectomy. I am not saying it can't be done -- just that I would be suprised but relieved.
At this point, I am just trying to understand what tools they can use to determine spread of the microinvasion. Right now I will hang my hopes on the dye.
Thank you for reading through this and offering your perspective. I truly appreciate it. It's going to be a long four nights waiting for Monday!
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