Recently diagnosed with high-grade DCIS -- so many questions

Options
2»

Comments

  • Hindsfeet
    Hindsfeet Member Posts: 2,456
    edited January 2011

    Thanks Beesie...I read your comment in tears...I think I could deal with a mx if I would wake up with a breast and nipples.

    I am seeing an oncologist next week, and a pain specialist. I hope these meetings will help me make the right decision. I am very tempted right now since it's a slow cancer to leave it be...and treat it with alternative medicine. I just wish the surgeon was willing just to take out the cancer, but she said it was a matter of time until I dx again. UGH.



    Binney4...thanks for the website, but right now, I just can't go there.

  • mom3band1g
    mom3band1g Member Posts: 817
    edited January 2011

    barry - I hear your pain and I am so sorry you are dealing with this. I know you will reach the decision that is right for you.  I wish I had some words to help/comfort you.  I will be thinking of you. 

  • Nana60
    Nana60 Member Posts: 60
    edited January 2011

    Hi Ladies. So many interesting and helpful posts here. I am just wondering if anyone was told they didn't need an MRI with DCIS. I asked my surgeon several times for an MRI prior to my MX and was told, "It is warranted in your case." Well, I ended up with positive chest margins and feel like my doctor would have had a better idea what she was dealing with if she would have let me have an MRI. Just wondering if anyone had a similar experience with their BS.

  • gymnut
    gymnut Member Posts: 37
    edited January 2011

    hi all,

    you can add me to the boston area contingency & i'm sorry any of us had to join this club though i'm very grateful to have found it.

    i'm also recently diagnosed w/dcis & at mgh but on the north shore.

    i haven't been on this site  in a few days & have since then done a lot more thinking & some further research, as well as followed up w/ both bs & rad onc.  i've now made my treatment decision & actually have re-excision scheduled also for jan 25! I'm still concerned about radiation but i definitely don't want mastectomy, my dcis presented as really small, nothing showed up on mri & bs only needs to go in to get one clean margin.  (had excisional biopsy after calcifications on mammo, during which she got all of the dcis but one margin not enough.)

    anyway, i was feeling really good about the decision....until the reality of the whole thing hit me a little harder.  yes we all have to go w/ out gut & mine was definitely telling me this. doc believes getting clear margin will not be a problem & i guess i'll feel much better after getting the clean report.

    good luck to all w/ whatever decisions & treatment.

    if people were serious about getting together....i'd probably be up for joining in.

    take care.  also, i might be interested in a recommendation of someone for a 2nd opinion if i need that.

  • LG300
    LG300 Member Posts: 652
    edited January 2011

    Nana - Many doctors don't do MRIs with DCIS.  I went to two surgeons for opinions and one recommended an MRI and one did not.  I went with the surgeon who recommended the MRI, and although it picked up two additional areas of DCIS, it didn't pick up everything and I still ended up having three lumpectomies without clean margins and then finally a mastectomy.  Sorry, I don't mean to scare those who are newly diagnosed - I'm the exception.  I did read though that 60% of DCIS patients who have lumpectomies don't get clean margins the first time.  Unfortunately, the surgeon can't see the DCIS, so s/he is basically going in blind.  The wires guide the surgeon to the correct spot and the mammogram or MRI give him/her an approximation of size, but unfortunately even an MRI often isn't sensitive enough to accurately show the extent of the DCIS.

    All - A few people were talking about survival rates for patients undergoing mastectomy vs. those undergoing lumpectomy + radiation.  Although the survival rates are similar, the recurrence rates are very different.  With a mastectomy, there is about a 1% risk of recurrence (it should be zero, but it's not), and with a lumpectomy + radiation, the risk of recurrence is about 10%.  Taking hormone-suppressing drugs if you're ER+ further reduces the risk of recurrence.  Approx. 50% of recurrences in DCIS patients are DCIS and 50% are IBC (invasive BC).  Even when the recurrence is IBC, it tends to be caught early, so it's treatable.  That's why the survival rate is basically 100% for DCIS patients whether they initially choose to have a lumpectomy + radiation or a mastectomy.

  • SuebeeBC
    SuebeeBC Member Posts: 1,256
    edited January 2011

    gymnut - Im glad you have come to a great decision for you.  The whole thing is so difficult.  Even though I am at peace with my decision, its still hard and I still question.  But I know I have to be strong and have some faith.

    LG300- thanks for the stats....Its amazing how many people out here talk about their recurrance.  I guess the good news is, after this we'll all be medically watched like a hawk!

  • louishenry
    louishenry Member Posts: 417
    edited January 2011

    Hi Barry,

    I'm so terribly sorry that you are going through this. I'm sure soon enough you will be on the other side of this, but in the meantime it's so frustrating.

    I also have hashimoto's. Most of us with hypothyroidism do. It's very common as you know. I don't have stats on this, but I'm sure that there are countless women who are hypothyroid that have had breast radiation all over the world.

    I did not have rads for my DCIS, but it had nothing to do with being hypo. I had several opinions on this and all the docs knew I was hypo and if my pathology was more aggressive, I would have had radiation.

    I do not know anything about RSD. Perhaps that is more the reason. I would make sure to double check with your endo or natural path regarding the Hashimoto's. I'm certainly not an expert, but it doesn't make sense to me.

    The only alternative stuff I do is the same stuff I did before DX. Some supplements- Vitamin D, fish oil, calcium. Exercise has always been in my life as well as a good diet. I don't know anything about iodine etc. What I do know about your situation is just what I have been reading.

    Your body keeps making cancer. Who knows why. It sucks for all of us-those with one cancer as well as several. You have been very fortunate that it hasn't (yet) been more serious. Maybe it's because of the alternative or maybe not.

    Because this is the DCIS forum and not the ALT  forum, I want to make a heartfelt suggestion. PLEASE PLEASE treat this. Get more opinions re radiation. Talk to other docs regarding MX. Not a natural path- an MD. Your DCIS DX was serious enough- this is even more so. Even if it's stage 1, it's still invasive. Now it's a different ball game.

    I truly wish you peace. A clear head to make the best decisions. I'm sure that your friends and family really love you and want you around for a long time.

    Best.

  • CrunchyPoodleMama
    CrunchyPoodleMama Member Posts: 1,220
    edited January 2011

    Barry, I replied to you on the alternative side urging you to do surgery for your IDC, not just alternative treatment... and you know I'm a completely gung-ho "alternative" girl... remember the bad-spot-on-an-apple analogy! Get it out AND follow alternative treatment!

    Although the survival rates are similar, the recurrence rates are very different.  With a mastectomy, there is about a 1% risk of recurrence (it should be zero, but it's not), and with a lumpectomy + radiation, the risk of recurrence is about 10%.  Taking hormone-suppressing drugs if you're ER+ further reduces the risk of recurrence. 

    I'm glad you pointed this out. And, they only quote short-term (5- to 10-year) survival rates. For those of us who hope to have 30, 40, 50 good years ahead of us, 10-year survival rate isn't good enough! That's why ultimately I went with what I unfortunately knew I needed to do... mx... and now that it's over with, I'm so very happy I did.

  • HantaYo
    HantaYo Member Posts: 280
    edited January 2011

    Namaste!

    Nana60:  For 20 years before DX I had the experience of many Bx that turned up B9 and one pre-cancer that was treated with local excision.  I knew that if DX with BC that I would choose bilateral if mastectomy was the recommended surgery.  Because my DCIS was in multiple areas my BS said I needed a mastectomy.  He said that because I was going for bilateral mastectomy it was not necessary to get an MRI.  I ended up with a pre cancer in the prophylactic side but do not know "if" it would have shown up on MRI.  It definitely did not show up on mammogram.

    Karla

  • louishenry
    louishenry Member Posts: 417
    edited January 2011

    Hi Crunchy,

    I have read your posts and am happy that your MX went well. Hopefully, you will be pregnant soon!!. I have two kids- a 19 y/o old girl and a 17 y/o boy and they are my whole life. ( my hubby too, of courseKiss).

    Based on Barry's posts, I assumed that she was planning on getting the cancer out. If she gets a MX and the margins are clear, then she may be good to go and use alt therapies to keep mets away. (hopefully). If she has a lumpectomy, even with clear margins, what alt therapies have a track record of reducing mets by roughly 50%? There is always the story that someone has done conventional meds and has a recurrence. It's terrible, but it's life. I know  western medicine does not have all the answers; however, the reason we have 97% recurrence free 5 years is because of our treatments that work. Based on my several friends that have had BC, radiation is a walk in the park compared to chemo. Also, I will never understand the comments that tamoxifen is a scary , scary drug. The vast majority use it with no problem. Myself included.

    I really worry about that advice. Like I said above, this is the DCIS forum and feel really passionate about it. I don't post much because I don't really have a lot of advice to give. Besides, Beesie is the best!  But really, she has had three cancers in about 3 years!  The thought of just having a lump and alt treatments scare me. It seems so irresponsible.

    I don't mean to sound rude. I feel badly for her.

  • CrunchyPoodleMama
    CrunchyPoodleMama Member Posts: 1,220
    edited January 2011

    louishenry, thanks for remembering that; you're so sweet! I'm asking my surgeon at my 5-week follow-up tomorrow for the all-clear to start trying SOON! Hopefully Barry will have surgery for the IDC, whether it's lumpectomy or mx... it sounds from her post above that her surgeon is pressuring her to go for a mastectomy... I think when a surgeon is putting pressure to do something you're not willing to do, it might be time for a second opinion!

  • Hindsfeet
    Hindsfeet Member Posts: 2,456
    edited January 2011

    For those who aren't sure what I am doing and why? First to say up to this point, my dx was dcis, grade 3, como-neurosis type...solid, ER + .... I know that I am now IDC...stage 1, low grade...ER+

    Since I've been on the dcis threads off and on for 3 years, I'm at home here. The only other threads where I've seem to made some connections is the alternative threads. Because I don't do standard care, I'm not sure I would fit anywhere else...at least for support.



    Why not radiation. At first the reason was cost, because I was self pay. It was expensive. After researching it...I realized if I had rads, and I had an recurrence, reconstruction would be difficult. I thought close observation would catch anything in my breast before it got serious. After reading many of the threads on radiation and further research, I wanted to avoid radiation all together.

    While researching RSD, I learned that radiation can cause my RSD to spread in the radiated nerves and muscles...bones. This was confirmed by my doctor. This is one of the reasons, my doctor prefers to do a mx, probably without reconstruction.



    Mx verses a lumpectomy:

    After having severe pain at times in the lumpectomy scars, I've become concerned about it being a localized RSD (regional pain syndrome). My pain doctor said several years ago to avoid surgery...

    So here I am. Lumpectomy is a small surgery. Mx is a huge surgery. At this point I am not willing to get a mx without immediate reconstruction. Mx is more of a risk for PMPS or RSD.



    Drugs: I am a natural girl. I have never liked drugs. I believe our body is smart and knows how to heal itself. It is my opinion that if we have a healthy immune system, we can make it. I do not want to take any med's that compromises or suppresses my immune system. It is obviously helping others, it's just not the road I choose to take.

    Funny enough...when I mentioned to my doctors associate that I have Hashiminto Thyroid Disease, she then said that I could not take the ..... drug given to prevent cancer recurrence. That was good news.



    So...the breast surgeon wants to wack off my breast. This is probably the best decision...emotionally I'm not ready and i am not sure if it is the right decision for me.

  • Beesie
    Beesie Member Posts: 12,240
    edited January 2011

    When discussing recurrence & survival rates after a mastectomy vs. lumpectomy + radiation, we need to specify if we are talking about invasive cancer or DCIS.  The considerations are actually different.

    My original comments in my earlier post were directed at voicewriter, who from her posts appeared to be concerned about having a lumpectomy if it turned out that invasive cancer was found in her next surgery.  My follow-up comments were in response to a post from barry, who was recently diagnosed with invasive cancer.  So I was explaining that for invasive cancer, survival rates are the same whether one has a lumpectomy + radiation or a mastectomy.  The reason is because it's distant recurrence (i.e. mets) that impacts survival for those who have invasive cancer and having a mastectomy does nothing to reduce the risk of distant recurrence.  So although local recurrence rates may differ, for those with invasive cancer, distant recurrence rates are the same if one has a mastectomy or if one has a lumpectomy + radiation.  If cancer cells have escaped the breast prior to surgery, having a mastectomy won't make any difference at all.  It's closing the barn door after the horses have escaped.  In fact a couple of studies have shown that distant recurrence rates may actually be lower for those with invasive cancer who have lumpectomies + radiation vs. those who have mastectomies.  

    "A local recurrence after mastectomy has about the same prognostic importance as a distant recurrence, and it is often assumed that a recurrence within the breast after radiation has the same implication as any other type of local or regional recurrence. The fact that the overall survival of patients randomly assigned to receive breast conserving therapy and radiation in these studies is equivalent to survival of patients who underwent mastectomy in spite of the higher local failure rate suggests that recurrences confined to the irradiated breast do not have the same prognostic importance as recurrences in the lymph nodes, skin and muscle."  http://www.rsny.org/200_PDFs/GSL-A-NEW-REPORT-IN-THE-TREATMENT-OF-BREAST-CANCER-MASTECT.pdf

    "Women with early breast cancer (no metastasis) who have breast conservation surgery (lumpectomy) followed by radiation are less likely to die of breast cancer within 10 years than women who have a mastectomy." http://www.healthcentral.com/breast-cancer/c/78/128782/lumpectomy

    Also, to the earlier comments, in many cases the survival rate stats that I've seen that show no difference in survival actually go beyond 5 years or 10 years:  "Women with relatively small breast cancers who were treated with breast-conserving surgery plus radiation therapy were as likely to be alive and disease-free 20 years later as women treated with mastectomy (surgery to remove the affected breast), two groups of researchers report in separate studies published in the October 17, 2002, issue of the New England Journal of Medicine."  http://www.cancer.gov/clinicaltrials/results/summary/2002/mastectomy-versus-lumpectomy1002

    This is the DCIS forum so I should have been clearer in specifying that I was talking about considerations related to the choice of mastectomy vs. lumpectomy + rads for those who have invasive cancer. Sorry if I caused any confusion.

    For DCIS, there is no concern about distant recurrence (unless a local recurrence is not found until it had advanced) so the parameters on which to compare a lumpectomy + rads vs. a mastectomy are slightly different.  

    Pure DCIS has a 100% survival rate if there is no recurrence.  50% of local recurrences of DCIS are not found until they are invasive. Overall the survival rate of those initially diagnosed with DCIS is 98% - 99%.  Since there is no risk of distant recurrence from DCIS, obviously this means that the women who do not survive had invasive local recurrences.  Therefore, for DCIS patients (unlike patients with invasive cancer), it's a local recurrence that is linked to survival rates.  

    It's true that the local recurrence rate generally is higher for those who have a lumpectomy + radiation vs. those who have mastectomies, but we have to be careful when we start quoting numbers. Lots of studies have shown what that the recurrence rate after a mastectomy for DCIS is in the range of 1% - 2% (assuming acceptable margins). The studies on recurrence rates after a lumpectomy + radiation are not nearly so clear or definitive. It may be true that the "average" recurrence rate is around 10%, but I've seen studies that quote a range from as low as 3% to as high as 60%. So any discussion about the merits of mastectomy vs. lumpectomy + rads for someone with DCIS needs to take into consideration the specifics of that individual's diagnosis and pathology - using the 10% average is almost sure to be misleading, either favorably so or unfavorably so. 

  • voicewriter
    voicewriter Member Posts: 51
    edited January 2011

    Gymnut -- I am definitely interested in starting a DCIS support group in the Boston area.  Let's do it!  This is so difficult to do alone, even with family and friends.  You are having your surgery on the 25th too!  I will be thinking of you :) 

    Beesie --

    Reading what you posted about possibility of women with lumpectomy and radiation are less likely to die than those with mastectomy is probably the last thing I needed to hear! LOL  More information to confuse me even more!!!  This is all so hard to figure out.  I wish I had a crystal ball!

  • Hindsfeet
    Hindsfeet Member Posts: 2,456
    edited January 2011

    voicewriter...hey, I'm sorry for hyjacking your thread. I didn't mean to. I assumed what Beesie wrote was for anyone considering a mx or a lumpectomy and based on what she shared, I thought it answered questions I had at that time. I should had figured that she was sharing from a DCIS perspective. I was dx with dcis twice. I really thought if i was ever dx again it would be another DCIS dx.

    In whatever choice you make voicewriter, please know that whatever treatment you choose, you must always be careful to continue screening. Last May they found nothing, and in December they found something.

  • Deirdre1
    Deirdre1 Member Posts: 1,461
    edited January 2011

    Barry:  I've sent you a PM - but I also want to say here in the open, for anyone else who is possibly in this position, that if you can't have a reconstruction because of potential rejection you are a PERFECT candidate for tissue reconstruction.  I'll look forward to your response to the pm...  and as always Beesie makes INCREDIBLE important comments!!!!

Categories