DCIS to Stage 4.....How does this happen?

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Faith123
Faith123 Member Posts: 41

Hi Guys,

I’ve been thinking a lot of my recent diagnosis with stage 4 Mets to spine;I keep thinking about what could’ve been done differently so that I didn’t have to end up where I’m currently at.

Please understand I’m in no means looking for anyone to blame, but I just can’t help wondering if there wasn’t an oversight with regards to my initial testing.

1.I was pregnant in 2016 and discovered a lump while I was pregnant and in Jan 2017 after giving birth was diagnosed with Widespread DCIS (no micro invasions)so basically pure DCIS,I had a mastectomy done(negative nodes) ER + PR + so basically no further treatment since I was told I’m Stage 0 and DCIS doesn’t spread

2. My oncologist put me on Tamoxifen of which I took for a while and then stopped cause of SE.

3.I got pregnant again last year and gave birth in November 2018.

4.May 2019 I’m diagnosed Stage 4 mets to spine(bone)

I’ve gotten a second opinion and the Oncologist is telling me that I should have my original specimen re-checked again because there actually might have been some Microinvasions.

How does this all happen? I keep thinking about this and I know things happen but it seems for me to get some sort of closure I need to know that things were done properly.

I was told so many time that DCIS does not SPREAD

And I just turned 30 this year so all of this is a huge shock still.

Comments

  • DivineMrsM
    DivineMrsM Member Posts: 9,620
    edited July 2019

    Faith, I don’t have answers for you. I hope you don’t mind my saying how much that sucks that you are dealing with mbc at such a young age. Your questioning is very normal. I think the mind goes through a process, trying in some ways, to make sense of it.

    Because of your age and because you initially were diagnosed with dcis, your doctors probably thought “no way” your prognosis would develop into anything further. I mean, I’ve read numerous articles where some in the medical field feel dcis is often dealt with too aggressively and that those diagnosed with dcis and go through with surgery and chemotherapy are going overboard.

    Consider the fact that it’s possible that you or your medical team could have done nothing different to prevent the progession to mbc from happening. There is a wild card element to breast cancer, and no one can say with any certainty which women will eventually become metastatic and which ones will have the bc eradicated forever.


  • posij3
    posij3 Member Posts: 10
    edited July 2019

    Faith123,

    When you were diagnosed, did your doctor do a diagnostic mammogram, an ultrasound, or an MRI?

    I'm asking because my OB-GYN doctor, Dr Cherie Schwartzenberg, did my annual PAP in Oct 2006 and while doing the breast exam, found what she thought could be a first sign of BC where she said if it was BC, could still be DCIS. We did a diagnostic mammogram which the radiologist found was negative for BC. Then she had me visit a BC surgeon to do an ultrasound; he found nothing in the spot she highlighted. I asked him if I should have a needle biopsy of the spot to be extra sure. He said "I wouldn't know where to stick the needle. There is nothing there-go enjoy your birthday".

    So I did and begin doing weekly breast exam checks because it had scared me. I was 42, dating someone seriously and it worried me a little that I'd "dodged a bullet". 3 months later in January 2007, in the exact spot she had noted, I found a very small lump, about the size of a BB. Called her and she sent me back to the radiologist, he saw something and ordered a core needle biopsy. It was BC, stage 1, grade 3 since it was lymph node negative, ER/PR - and 1 cm. The grade 3 was due to high level of mitosis (10+) occurring under microscope. Because mine was triple negative, they didn't have great protocols since it isn't as common. One doc suggested 4 rounds A/C, another 4 rounds of A/C, then 4 rounds taxol, 45 days radiation.

    I am skeptical of practicing chemo on women right now. I say this because A/C study 6/2007 shows 8% success for early stage BC but they are still actively doing that course of treatment. Still researching what is "standard" course of treatment, if that exists.

    I say all of this because my hope is that after 12 years since my care, they are now doing MRI's to ascertain instead of just diagnostic mammograms. When I asked my BC doctor if an MRI would have caught my BC while it was still DCIS instead of waiting 3 months for it to grow into a Stage 1, he said the MRI would have but insurance wouldn't have covered it. That is unacceptable. Let me decide if it's worth battling my insurance or paying it outright.

    We have to demand better outcomes, better preventative care. instead of costing me/my insurer $1800 for an MRI for proactive care, my care was $250,000 for 8 rounds of chemo, 45 days of radiation. Just want to make sure things are getting better and women are being most informed.

  • Beesie
    Beesie Member Posts: 12,240
    edited July 2019

    I am not Stage IV, so my apologies for intruding on the Stage IV forum.

    Faith123, I am so sorry about your Stage IV diagnosis.

    It is very rare for this to happen as you describe, although there are a few possibilities that might have led to this. The first and most likely scenario is that your original diagnosis did in fact include a small amount of invasive cancer that was not discovered by the pathologist. The fact that you presented with a lump when you were diagnosed with DCIS is unusual - DCIS does not usually present as a lump and when it does, it is much more likely that there will also be some invasive cancer present. While on average approx. 20% of preliminary DCIS diagnoses (via a needle biopsy) are upgraded to invasive cancer once the final pathology is done, according to the following study, 49% of those who presented with palpable DCIS ended up with an invasive cancer diagnosis:


    Should palpable DCIS be treated as IDC? A retrospective audit.


    You also mentioned that you had widespread DCIS; this too is more likely to indicate the presence of a microinvasion or a larger invasive cancer. The following study shows the significance of both size of the DCIS and palpability as being key factors that significantly increase the risk that invasive cancer will be present:

    A Simple Model to Assess the Probability of Invasion in Ductal Carcinoma In Situ of the Breast Diagnosed by Needle Biopsy


    Another possibility is that you may have had an occult invasive cancer somewhere else in your breast, separate from the DCIS. Although the pathologist should look thoroughly at all the breast tissue removed, it is possible that the areas of tissue not directly involved with the DCIS might not have been checked quite so carefully.


    Did you have a BMX or a UMX? If you had a UMX, the question is whether you might have an occult invasion in your other breast. If you still have a remaining breast, I trust you've had an MRI? If you had a BMX, here again it's possible that the breast tissue in the non-cancer breast was not as thoroughly checked through by the pathologist, and a small invasive cancer could have been missed. Not likely, of course, but it is certainly more likely that the mets sourced from an invasive cancer rather than from the DCIS, so all the possibilities for where an occult invasion might have been hiding should be considered. With a BMX, there is a lot of breast tissue to look at under the microscope, and missing a tiny 1mm or 2mm invasive cancer is certainly possible.

    Is your current diagnosis HER2+? I ask because if you did have an occult invasion and it was HER2+, that would have been a small but aggressive invasive cancer, which could lead to your current diagnosis.

    Unfortunately, occult invasions happen with DCIS. Not common, but common enough. Most of the time there is no negative impact but sometimes women are found to have positive nodes despite finding only DCIS in the breast, and sometimes, as happened with you, mets develops despite finding only DCIS in the breast.

    Again, I am so sorry that you are dealing with this at such a young age, and with two young babies. I wish you every luck with your treatment.




  • NicoleRod
    NicoleRod Member Posts: 2,906
    edited July 2019

    Well as Beesie knows...I also was Stage 0 Insitu 2015... only 3 cancerous calcifications supposibly completely contained in the milk duct... 4 years later ...bone and liver mets... so I know how you feel.

    I believe either some of those cells escaped...or as Beesie also knows after looking at my original surgical lumpectomy report it looks like they should have cleared wider margins...so that is probably the culprit in my case.

    So sorry you are dealing with this. I feel your shock and pain ((((((hugs)))))

  • Beesie
    Beesie Member Posts: 12,240
    edited July 2019

    Nicole, your case is a bit different than Faith's because you had a local recurrence, which included invasive cancer and DCIS, at the same time that you had the metastatic recurrence. So while the development of mets in your situation is just as devastating, it followed a more expected and understood route, DCIS --> IDC (in breast recurrence) --> Metastatic recurrence. When DCIS recurs locally, in about 50% of cases the recurrence is not found until after the cells have already evolved to become invasive cancer. And in an extremely small number of those cases, the invasive cancer has spread and metastasized before even the local recurrence is diagnosed.

    To your point, because you had a fairly large area of high grade DCIS and almost involved surgical margins after your original DCIS surgery, it's quite likely that some DCIS remained in your breast. No one can know when those cells evolved into IDC, but it could have been anytime time after your first DCIS diagnosis. As soon as those cells became IDC, they had the ability to spread/metastasize, so you may have had a small area of IDC for in your breast for years before it became large enough to be found as a local recurrence. A more understandable sequence of events that Faith's, but equally shocking.

    Again, my apologies for posting in the Stage IV forum.

  • Faith123
    Faith123 Member Posts: 41
    edited July 2019

    Hi Beesie,

    Please feel free to always comment on my questions,I honestly don’t mind and you’ve bought a lot of clarity to my situation along with everyone else who has commented.

    Thank you sooo much guys .

    Currently on chemo (AC) and I’m feeling terrible.

  • NicoleRod
    NicoleRod Member Posts: 2,906
    edited July 2019

    Beesie, once again you are awesome in your explanation!!! I miss chatting with you!!! I too would never mind you being here to chat in Stage IV :)

  • Moderators
    Moderators Member Posts: 25,912
    edited August 2019

    Faith123, we're thinking of you. Actually, we're thinking of ALL of you and extremely grateful for all the wise words and support here

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