Any ER-, Pr-, Her2 positive with node involvement

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KitCat1
KitCat1 Member Posts: 53

Hi all,

Just finished chemo and rads and now on Hercepton only. Needing to hear some encouraging, positive stories!

Comments

  • LJ13-2
    LJ13-2 Member Posts: 235
    edited December 2010

    ER-/PR- HER2+ and just passed my 3-year anniversary.

    I did Herceptin for a year, finished in Jan. 2009. 

    Feeling good, mammos and tests all come back clear, keeping my fingers crossed that it stays that way.

  • fightinhrd123
    fightinhrd123 Member Posts: 633
    edited December 2010

    me :) i had pos nodes b4 chemo, but none after.  I was diagnosed may 2008.

    Laura

  • TammyLou
    TammyLou Member Posts: 740
    edited December 2010

    Yup.

    Locally advanced breast cancer with fixed matts adhered to my chest wall in January 2005.  ER/PR neg.  HER2++++  12+ positive nodes.

    So far, so good.

    tl

  • KitCat1
    KitCat1 Member Posts: 53
    edited December 2010

    Thank-you ladies! I needed to hear these stories. All the negative about being ER- really gets me down! Any positive notes on being ER-? Thanks all and carry on , move forward! Here's to growing old!! XOX

  • LJ13-2
    LJ13-2 Member Posts: 235
    edited December 2010

    KitCat, my onc told me that if I make it to 5 years, the chances of recurrence of this breast cancer are pretty much nil. That is not the case with ER+ breast cancer.

  • blondie45
    blondie45 Member Posts: 580
    edited December 2010

    TammyLou - What treatments did you do? Did you have a mastectomy?

  • weety
    weety Member Posts: 1,163
    edited December 2010

    I have read that ER- responds better to chemo AND I just recently read that herceptin works better in ER-.  How's that for good news for ER negative?  (I'm ER+ but only "weakly" so my percentage is probably only 5% or so)

  • KitCat1
    KitCat1 Member Posts: 53
    edited December 2010

    Thank-you once again ladies, excellent info and points. I had right breast mastectomy,, 6 x TCH, 25 rads, completed chemo in September, rads in November and now on  Hercepton every 3 weeks until June. My onc says the odds are defineately in my favour. It's good to meet you all and thanks for the input. Sometimes I can get so down..... ( the unknown) ... you know what I mean.... positive stories are always welcomed! XOX Onwards and Upwards I say!

  • KitCat1
    KitCat1 Member Posts: 53
    edited December 2010

    Excellent News Weety! LJ13-2 thanks.....!

  • RebzAmy
    RebzAmy Member Posts: 322
    edited December 2010

    Hi KitKat

    Diagnosed June 2007 HER2 positive with several lymph nodes involved and one very large one. It's now 3 1/2 years since diagnosis and 3 years since end of chemo and operation and 2 years since finishing herceptin.

    Hope this helps

    xx

  • leftfootforward
    leftfootforward Member Posts: 1,726
    edited December 2010

    I am 37 years old have 4 children (8, 5, 3, and 4 months) and was just diagnosed with ER-, PR-, Her2 + with node involvement.  I am scheduled for surgery just after the new year followed by chemo and then radiation and herceptin.  It looks to be a long road and I stumbled across this website and forum.  It helps to read your responses and stories.  I am currently struggling with weaning my 4 month old in preparation for the surgery and chemo.  

    thanks for being a source of encouragement. 

  • lkc
    lkc Member Posts: 1,203
    edited December 2010

    I am 5 and one half years out and doing great. The whole cancer ordeal sucks, you will get through it.

    I love life and am grateful everyday for  the new txs that are avialable.

  • KitCat1
    KitCat1 Member Posts: 53
    edited December 2010

    Thank-you IKC and others for your positive input! I need to hear it! We all do! xo

  • imatthew
    imatthew Member Posts: 206
    edited December 2010

    see my wife's diagnosis below, 1 TCH done, next one is wednesday.

  • Letlet
    Letlet Member Posts: 1,053
    edited December 2010

    Hi ladies...I was just wondering if your onc is prescribing Tamoxifen after Herceptin. My bx report states ER- and PR 60% (weak). I just read that Tamoxifen suppresses estrogen only. When my onc told me about giving me Tamoxifen for 5 years I thought it's because it worked on progesterone too and apparently this is not the case so I'm confused as to why she would prescribe me this. I would hate to be on something with so many side effects if there was no point in me taking it anyway!

  • nagem
    nagem Member Posts: 353
    edited December 2010

    More than 5 years since diagnosis. Doing well. Good luck!

  • KitCat1
    KitCat1 Member Posts: 53
    edited December 2010

    Hi Letlet,

    I'm not sure on that one. From what I know Tomaxafen is for the estrogen receptor. Ask your onc. Don't be afraid to ask questions. Knowledge is power.Nagem... WAY to GO!!!! Yay another sister doing well! So happy for you!

    '

    Huge hugs to all! xo

  • weety
    weety Member Posts: 1,163
    edited December 2010

    I don't think many women are ERneg and PRpos.  I think it's usually the other way around.  Hmmm. . .   I think you should start your own post on this, putting your er/pr status in the title so you can find as many other women that have this same diagnosis.  Also, why do they consider 60% weakly positive?  My ER was weakly positive, and although the path didn't give numbers, my onc said that means it's probably only 5-10%.  60% doesn't seem very weak to me.  Just curious.

  • Leslie1962
    Leslie1962 Member Posts: 233
    edited January 2011

    I am ER/P neg and HER2+++. Had double mastectomy (left side cancer only), left axillary dissection, Adriamycin, Taxol, Cytoxan, Taxotere, Herceptin, radiation. I am down to my last few Herceptin infusions and doing well.

  • elenalb
    elenalb Member Posts: 8
    edited January 2011

    Wow Leslie,

    Your diagnosis/treatment sounds nearly identical to mine.  I had cancer only on the right side, 6/19 nodes, IDC, grade 3 (whatever that means), ER-/PR-, HER+++, but had a radical bi-lateral mastectomy in July 2010. Diagnosed 3/10, first chemo (before surgery) was A/C, then surgery, then 12 weeks Taxol/Herceptin, now I'm half way done with radiation.  I could only do 12 weeks of Herceptin, as my MUGA scan went from 57 to a 38 in 14 weeks.  My oncologist won't put me back on Herceptin, but I made him refer me to a cardiologist who ordered an eco-cardiogram, which showed my heart function at 60%.  So that's my next battle, trying to get my oncologist (I have Kaiser so they're all connected) to allow me to gauge my heart health by eco-cardiogram rather than MUGA.  The cardiologist was a bit amused that oncologists still use MUGA scans as they can measure your heart, but some other organ in the same vicinity giving false results.

    When I had my MUGA scan showing I was in "heart failure" at a 38% efficiency, I was walking several miles each week and working out on a treadmill at the gym (a recent accomplishment of mine).  I sure didn't feel like I was in heart failure....so the two of them won't consult on this.  I don't think the cardiologist wants to get in a "pissing match" with the oncologist.  The oncologist said after radiation that I was just to "get on with my life", he would not be doing any tests, etc. except an occasional blood workup.  So now I'm scared to death that this could reoccur and they won't catch it in time to do anything about it (don't know if there is anything else to do since they've thrown everything they had at me.

    Comments anyone?  Thanks.

  • Leslie1962
    Leslie1962 Member Posts: 233
    edited January 2011

    elenalb - All I can say is maybe get another opinion on the heart function. I just had another echocardiogram that showed my left ventricular ejection fraction in the 50-55% range. I was still cleared to continue with my last few Herceptin infusions. It certainly sounds odd for you to be in heart failure while walking so much. Are you short of breath or anything like that? I too was told to go back out into the world and live my life. Once herceptin is done in February I think it will be difficult to know that lifeline, so to speak, will be done with. My doctor also does not do scans etc., unless there is a true reason to "go fishing", as he likes to call it. He said it usually finds some oddball stuff that you didn't even know you had and have been living with all your life. Don't need the extra radiation, special dyes and the anxiety that scans put people through. I am having major problems with lymphedema since axillary dissection. Have you been experiencing this or are you one of the lucky ones with no problems/symptoms? Hope you are doing well. Keep me posted on the heart function. Have a great week!  Wink

    ~ Leslie

  • KitCat1
    KitCat1 Member Posts: 53
    edited January 2011

    Hi Leslie. the oncs that I see said the same thing. No more scans , etc, unless warranted. ( you have complaints) I was having aching , back pain, they assured me it was nothing, but I insisited on the bone sacn and they did it.... it was nothing. I finished chemo in October and apparnatly these efeects can saty with you for 6 to 9 months. Also scans can give off neagtive results , causing worry and stress when not neede. i hear ya though, it seems like others are getting scanned all the time???? i think if you push, you will get. I  am in Canada and we have it all covered, so its not a make money issure here. When i was first daignosed I had bone scan, ultra sound of all organs and chest xray. I also had a ct injected dye scan on my liver for a mark that was there that turned out to be a birth mark. So moving forward..... during erecepton like you. I am tired though, I miss my energy. I just stated with a personal trainer so hopefully this will get me up an going.Your doc is right, we don't need extra scans for no reason, unless warranted. I hope All is well!! It's 2011... good riddance 2010, lets live LIFE!!!!!!

    Big Hugs XOX

  • jacee
    jacee Member Posts: 1,384
    edited January 2011

     Letlet said-

    I just read that Tamoxifen suppresses estrogen only. When my onc told me about giving me Tamoxifen for 5 years I thought it's because it worked on progesterone too and apparently this is not the case so I'm confused as to why she would prescribe me this. 

    Letlet, I just had this conversation with my endocrinologist this week. I am 97% ER and 90% PR. Yet, I never hear anything about progesterone suppression, only estrogen. He said,"that's because the only way you get progesterone, is as a by product of estrogen. If you take away the estrogen, then so goes the proesterone."  Hope this is accurate info...made sense to me.

  • TriciaK
    TriciaK Member Posts: 362
    edited January 2011

    I had three positive nodes, highly triple pos and five and a half years out and doing well:)

     Good luck!!!

     Tricia xx

  • medinorth
    medinorth Member Posts: 67
    edited January 2011

    I asked on another forum about mastectomy vs lumpectomy. I am also ER-/PR- and HER2+ but I had lumpectomy + re-excision and will have chemo and rads soon. I've read that node positive leads more onc to recommend AC-TH over TCH, but that the decision is determined by other things, including some regions of the country preferring one over the other. I am grateful for the wealth of information, but I really wish there was a better, more precise guide to these things. It has taken me a few weeks to get to all of the different forums. Besides my diagnosis and treatment, manuvering breastcancer.org has been a stressor.

  • TriciaK
    TriciaK Member Posts: 362
    edited January 2011

    Medinorth,

     A lumpectomy with rads gives the same overall survival stats but does have a slightly higher rate of local recurrance!

     Tricia x

  • ALK
    ALK Member Posts: 46
    edited December 2011

    Thank you for such positive news.

  • lkc
    lkc Member Posts: 1,203
    edited December 2011

    Hi ladies, Just wanted to update you all. I am now " out' over 6.5 yrs from a stage IIIC er, pr neg& Her2 pos BC." Awful " prognosticators at Dx , and now I am NED and happy as a clam. Take heart, and please know there are quite a few us  long timers out there once again busy with our lives and living well beyond the daily terror of BC.

  • Momof2inME
    Momof2inME Member Posts: 683
    edited December 2011

    Thank you! Thank you!! I am having BMX next wednesday and these stories are amazing!! I am so scared there will e positive nodes. To "hear" all of you gives me hope and inspiration! You are all so strong and amazing to me!!

  • mauimom
    mauimom Member Posts: 80
    edited December 2011

    thank you for the positive updates!  they really help...

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