Large area of DCIS & possibility of microinvasion
Hello All,
My first post here...have read a lot on this site...and you ladies are awesome! Thx for sharing so much good information, insight and support!
I was diagnosed with a 6cm area of DCIS in 1 breast. Am having a double mastectomy w/an SNB. I know I'm at higher risk for invasion. Does anyone have insight/experience on having the invasion? When is it diagnosed? What is the usual forms of treatment? Radiation, chemo? Thank you sooooo much!
Comments
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jammie,
I just 'bumped" a post from a very knowledgeable poster named "Beesie" on understanding DCIS. If you haven't read it yet, it is excellent. She herself had a 6 cm DCIS and after pathology did have microinvasion. Hopefully you can connect with her on these boards.....but I'd try not to panic. I had a single mastectomy 2 yrs ago for 4.5 cm DCIS, some grade 3, and turned out to have pure DCIS after the surgical pathology was completed, so hang in there.
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jammies - Definitely check out the post noted above. Very good information.
At the time of my diagnosis, my DCIS was thought to be 6.5 cm. I had a BMX and SNB on May 24th. My pathology report indicated a very small amount of microinvasion and my nodes were clean. I've met with both an oncolgist and a radiation oncologist (with an upcoming 2nd opinion from a radiation oncologist). Even with the little bit of microinvasion I will not have to have any chemo or drugs but most likely will have to have radiation. The radiation is recommended because of a narrow margin and the grade (3) of my DCIS and not because of the microinvasion. Oh, and my DCIS turned out to only be 3.2 cm - one nice surprise!
Reading on here....I think in the DCIS with HER2+ microinvasion thread, that with small amount of microinvasion that it is treated just the same as pure DCIS.
Try not to overthink too much (easier said than done...I was nuts the last two weeks before surgery) and just have faith that all will be well. PM anytime if I can help with any questions.
take care,
Juls
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Hi jammies,
I'm new here too and recently diagnosed with DCIS when 3 areas of microcalcifications (right breast) where found on my very first mammogram. I only had one of the 3 areas biopsied and the result I was given was an extensive area of low grade DCIS. I opted to pass on a lumpectomy and go straight to MX. I will be having a MX and SNB on the 28th of this month, all being well.
From what I have read here and know from a friend who also had DCIS, they can't really be certain what 'lies beneath' until the final pathology following MX. My friend was initially told after core biopsy that there was only a small area of DCIS but they couldn't get clear margins following a lumpectomy and she had to have an MX. The final pathology found 4.5cm of high grade DCIS but thankfully no microinvasion or lymph involvement. So like you jammies, I will have to wait until the final lab report to get the full picture and yes I know exactly how you feel, it is a very anxious wait.
Hugs,
Aggie
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Hi, I don't have any advice but I am in a similar situation--DCIS with a "Strong suspicion" of micro invasion. I'm having an MX in 3 weeks, I don't think they'll know for sure what's going on until the final pathology. Like you, I am very nervous about it! Best wishes...
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Hi,
I had a relatively small area of DCIS. My excisional biopsy discovered low grade DCIS and 2 tiny invasive areas....1mm and 4mm so I was lucky that it was caught so early.
My treatment was another lumpectomy to clean margins and SNB.
I did radiation and tamoxifen...so far on tamoxifen for 3 years and still hating it.
My tumor was grade 1 and chemo was not recommended due to tiny size and grade.
Hang in there - you won't know until they take it all out. Once you do know you will have an action plan and will feel better!
Hugs...Kosh
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Julianna51...How long did your pathology report take after BMX? The absolute worst part of this for me is making myself sick waiting for test results... I am having BMX w/ SNB on July 1st and not even worried about the surg. and reconstruction.. I know the waiting for the path. report is going to drive me back to how horrible I felt right after this all started and freaking out everytime the phone rang. My first path report said 2 areas of DCIS grade 3, had my slides looked at by a path at Sloan down graded one area to grade 2, but the other area said there is a suspicion of microinvasion, but not diagnostic...ugh!!!!
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I found out about the invasion one week post mastectomy, when I received my final path report. You should also get the news when you get your final pathology. Your doctor should be able to give you a sense of when you will get the report.
To reassure you, a micro-invasion is usually not a big deal. It is small enough that you shouldn't require any change in your treatment, and it wouldn't have much affect on your prognosis. Your staging would change from 0 to 1, and you would have a slight (like 1% or less) chance of things spreading, but in general things would be the same as if they just found DCIS.
In terms of treatment, you might get radiation if your had poor margins after surgery, regardless of type of cancer near the margins. You might get chemo if they found a large invasion or possibly an invasion that was HER2+, or if they found cancer in your nodes. Micro-invasions are 1mm or less, and well below anyone's criteria for chemo.
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Hello All!
Thanks for the great info and effort to share what you know!
My surgery is scheduled for 7/20. Well...here we go!
I look forward to sharing my learnings with others as you've shared yours' (and support) with me!
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I was diagnosed with DCIS in May. Multi focal, >6cm, grade 2 and 3 with necrosis. I am also small breasted so a lumpectomy was not possible, I chose to have bmx with te done on June 8th. I also was fearful of microinvasion.
My final pathology report ended up showing 7.6cm of calcification and no microinvasion. 3 sentinel nodes lit up, removed and they were clean too. I am cancer free. No chemo, no rads, no tamoxifen. Keep your chin up.
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From what I understand, if you have pure DCIS and clean margins after your mastectomy, radiation is not needed and chemotherapy is not standard treatment for pure DCIS. If margins are not clear, I have read of women having to have radiation even after the mastectomy.
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mycinnamon, it depends. Most doctors use the Van Nuys Prognostic Index www.theeffectivetruth.info/wksht1.html to determine whether radiation is needed for a DCIS case. It looks to me that you're at least an 8, which would mean that radiation would be recommended. Here's the decision chart: www.theeffectivetruth.info/brcavnpi.html
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It is true, mastectomy does not gaurantee no further treatment for DCIS. I had BMX with TE's on 5/26 for DCIS in right breast, it turned out to be extensive DCIS 6.5cm and my margins against my chest wall are between 1-2mm.....BS said no further treatment needed, but others on here say rads is often given. I have appt with RO on 7/21. Whatever your decisions are, know that it doesn't mean things won't change, and we all have to prepare for it. Best of luck!
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FYI...surgery moved up to 7/13...I'm jazzed...not my first choice of things to have to do...but ready to get moving with this process! Thanks for all the insight!
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I had a singel mastectomy (no recon) in April, 2007 for a large area (6cm+) of DCIS with "several areas suggesting microinvasion". My surgeon told me that "small amounts of real cancer" had been detected in the lumpectomy and to prepare myself for the possibility of chemo and/or radiation. It was a relief when the final pathology (from the mastectomy) declared that no microinvasion was found. I suppose that meant that the small areas of microinvasion were removed during the lumpectomy. Just had my 4th checkup since the surgery and all was clear. I'm well into my 5th year post diagnosis.
My very best wishes for a successful surgery and hoping that you won't need any further treatments.
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I had 2 lumpectomies with unclean margins so I went for a BMX on 3/28/11. Cancer was only on the left side but I was tired of the whole process. I do not regret my decision. Currently have TEs. I did have 2 areas of microinvasion but I have been seen by my oncologist and Duke University. I also consulted with John Hopkins. All have agreed that my microinvasion was so small (less than 1mm) that no chemo/herceptin/tamoxifen recommended. My margins were clean after BMX so I did not need radiation. Now I am just waiting for exchange surgery. Good luck to you. Getting a second opinion did help put my mind to ease on what I should do.
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Thanks for sharing your experiences. I am thrilled with my BS (he was my second opinion and one of those "THE" surgeons everyone wants to get into). Question that I should probably know the answer to: What are "margins?" And what does it mean by "clean" margins. Thx!
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Others can probably explain in more detail about clear/clean margins, but basically it just means that you have no areas of cancer remaining after they remove the breast tissue. I still had areas of cancer after my lumpectomies so I had no choice but to have a mastectomy. I did decide to have both breasts removed even though I only had a problem on the left side. Hope this helps
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Hello All!
Today is my BMX & SNB & immediate recon surgery! Here I go! Thanks again for all your support!
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Praying for a quick recovery!! Hugs, Lynette
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