Have stage 2B....what will be next?

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Kimberchick
Kimberchick Member Posts: 26
edited June 2014 in Stage I Breast Cancer

Hi, I just got my path report back and I am stage 2B.  I have not yet scheduled an oncologist appt., but I do know I am estrogen and progesterone positive, HER2 negative.  Do you think I will be having chemo or radiation?  The tumor was 2.5 cm and there was a tiny bit in the one sentinel node they removed.  The surgeon said there would be no more surgery.  I assume I will get hormonal therapy, like tamoxifen, but was wondering about other chemo?

  

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  • Letlet
    Letlet Member Posts: 1,053
    edited May 2011

    Kimberchick I was diagnosed last year, it seemed like the world crashed around my head but 8 months of treatment (surgery, chemo, radiation)...I am still standing and I made it out of the long, long tunnel that I thought would be forever.

     A 2.5 cm is of considerable size and I believe you will be offered chemo (of course I am not an oncologist). I would try to get a consult with an onc as soon as possible...although some doctors wait some weeks post surgery for the body to heal before starting chemo.

  • Kimberchick
    Kimberchick Member Posts: 26
    edited May 2011

    I think you misunderstood me....I am both estrogen positive and progesterone positive.  HER2 negative.

  • kira1234
    kira1234 Member Posts: 3,091
    edited May 2011

    Kimberchick, Did your BS or Onc. run the Oncotype test on you tumor. It will help your Dr. decide if chemo will benefit you or not.  As far as radiation that will be decided by you Dr's as well. If you had a lumpectomy radiation is normal procedure.

  • edwards750
    edwards750 Member Posts: 3,761
    edited May 2011

    Agree with Kira about the oncotype test. My ONC recommended it for me because she was ambivalent about my treatment plan. I am so glad she did. My score was low and my cancer was not aggressive so I am doing radiation; however, my tumor was really small like less than a centimeter. I did have a micromet in the SN though but because of the test score she decided I didnt need chemo. I would ask my Onc about having the test done. It is very expensive but fortunately our insurance co paid for it - it is like over $4k. Keep us posted.  diane

  • judyfams
    judyfams Member Posts: 148
    edited May 2011

    The usual decider about chemo is the oncotype test.  Ask your onco to have the test run on the tumor already removed to help determine if you need chemo.

    Also you will need radiation if you had a lumpectomy. Definitely ask your radiation oncologist if you are a candidate to have it done in the prone (face down) position instead of the supine (face up) position.  In the prone position the armpit and the ribs and the heart and lungs are not touched by the radiation.  The breast hangs down and the radiation comes from the right and left sides and not from above.  I had my radiation done that way and do not know why it is not done more.  I know one has to be a candidate for it - breast large enough to hang down (I'm a C) but the hospital facility would not even discuss the prone position with me even though I knew I was a candidate - so I went elsewhere and found a facility that did it for me that way.

    The hospital said if I did it in the supine position they would protect my chest and ribs.  But think about it - which gives the chest and ribs better protection - radiation coming from above you aimed at your breast or radiation coming from each side aimed at the breast?

    Judy

  • jessica749
    jessica749 Member Posts: 429
    edited May 2011

    OF course I am not an oncologist, but if you are stage 2b - given your tumor size of 2.5 cm, then there IS lymph node involvement, however small. Therefore, you will get chemo, I would think.

    The oncotype dx test does not seem to apply to you: if you look at the  website (google oncotype dx and read the website about 'who' this test is for),  apparently it helps determine if node negative, estrogen postive early stage bc can benefit from chemo. The implication then is that node positive bc can benefit, there is no big gray area as there has been for node neg.  The whole point of oncotype dx test i think is to help prevent medical community from overtreating so many bc's (which they now do of course, since it can be deadly and it's hard to judge recurrence). For me personally, while chemo is scary, more scary is under-treating me.  I am the kind of person who wants to know that I brought all the guns to battle...I never want to be regretting there was someting I 'should' have done...Good luck

  • Kimberchick
    Kimberchick Member Posts: 26
    edited May 2011

    Ah, good information!  Thanks!  I agree, KSD, that under-treating me is more scary.  I forgot to mention I had bilateral mastectomies.  So do you think I will not have radiation?

  • lago
    lago Member Posts: 17,186
    edited May 2011

    KSD not all stage IIB has lymph node involvement. I'm 2B with no nodes.

    Kimberchick They typically give an oncotype test for early breast cancer (stages I-IIIA) that are node negative and HER2/nue negative. It sounds like you have micromets in your node so I believe you would still be eligible. The reason why they do this test is because there is a possibility you may not need chemo… the oncs really would prefer not to over treat some one. The test also takes into account your tumor grade (1-3). The higher the grade the more likely you will might need chemo but still there are many more factors to consider.

    I didn't have the test because I am HER2+. HER2+ get herceptin which is more effective with chemo. The onco test is expensive so they don't test you if you are going to have chemo anyway.

    I had 6 rounds of chemo (Taxotere, Carboplatin). Last one was Jan 18th. It really wasn't as bad as I thought. The last 2 rounds were harder but still doable. I was exercising all through the 1st 3 rounds. Slowed down round 4. Round 5 & 6 gave up a little but part of too was it was winter and cold out.

    Hang in there and let us know how it goes.

  • Kimberchick
    Kimberchick Member Posts: 26
    edited May 2011

    Lago, good to know.  I did have micromets in SN.  So do they consider that "node negative" to be eligible for the Onco test?  Also, does it depend if I am post-menopausal?  So glad you were able to tolerate your chemo so well.  You are amazing!  Did you lose your hair?  

  • sundermom
    sundermom Member Posts: 463
    edited May 2011

    I am 37 and also dx stage 2b.  My primary tumor was 2.2 cm and a had a micromet in each of the first two nodes.  My onc says he always recommends chemo for node positive ladies and that the Oncotype test is not applicable as soon as they find ANYTHING in the nodes.  I finished DD A/C x4 followed by DD Taxol x4 two weeks ago.  I had a BMX before chemo started (December 2010)and will be starting radiation in the next couple of weeks.  I will also take Tamoxifen for 5 years and then most likely switch to an AI for 5 additional years.  I have had a relatively easy time with all treatment so far and am willing to do anything that will provide ANY additional extra insurance against a recurrence.  I have 5 young children (10 and under) and want to be here for them for the next 50 years. 

    Tammy

  • Kimberchick
    Kimberchick Member Posts: 26
    edited May 2011

    tsundermann, thanks for the good info.  I'm surprised you had mastectomy yet are still doing radiation?  

  • lago
    lago Member Posts: 17,186
    edited May 2011

    I don't know but I would think you could get the test with micromets. Good question to ask your onc. It doesn't matter if you are pre or post menopausal but you do have to be ER+. I really don't know a whole lot about this test because I was ineligible. It's a nice test to get though because I hear it give you more specific information based on your tumor rather than these general stats on stages.Push for the test if your insurance pays for it.

     I'm not that amazing. There are lots of women that did well and worked out all through chemo. Remember that people will post more about having problems than not having problems on this site.

    I lost my hair. My eye lashes fell out 5 weeks after chemo but came in pretty quickly. The eyebrows thinned a little then started to fall out 5 weeks after chemo… but grew in about the same time so I never really looked like I was missing much. Just had to pencil in a little.  My avatar is a picture of me in my wig 2 weeks after my 4th treatment at a Bat Mitzvah.

    I wore my wig that weekend only. Wore scarves all the time. They looked pretty good on me. Right now I'm almost 15 weeks out from my last chemo. I've been going without anything since week 13. I did have colored though. Its of course very short but I'm actually getting compliments from people who don't know I've been through chemo. Don't have the heart to tell them this is the most expensive hair cut I've ever had but I haven't needed a cut since mid October Tongue out

    --------------------------------

    Mastectomy does not mean no radiation. I myself was in a gray area and surprised I didn't have to do it. Large tumors (over 5cm) usually do. Node invasion (not  sure micromets) usually do but depends on the number of nodes. Also your margins, how wide, where the tumor was etc. There are so many things to consider when it comes to radiation.

  • sundermom
    sundermom Member Posts: 463
    edited May 2011

    I have to admit that I, too was surprised to find out about having rads. I am having rads to clavicle area, axillary nodes (even though Level I and II (32 total) were removed), whole breast and 5 boosts to the scar line.  Given my age, node involvement and the fact I had LVI I am at a very high risk for recurrence.  My RO said adding rads to my treatment plan would drop my recurrence risk to less than 10%. 

    Tammy 

  • jessica749
    jessica749 Member Posts: 429
    edited May 2011

    Iago you are right not all 2B is node positive: but the 2b with a tumor size of 2.5 cm apparently IS, and I got this info.  off of this very website we are on...they have a section describing what staging is and means, and for cancer size 2.5 cm, if you are called 2b it's because you also have positive nodes.

  • sundermom
    sundermom Member Posts: 463
    edited May 2011

    Micomets is node positive.  The term micromet just refers to the size of the mass that was seen in the node.  It means it was less than 5mm.  Macromets are greater than 5mm.  I read this on my patholoogy report.

    Tammy

  • jessica749
    jessica749 Member Posts: 429
    edited May 2011

    kimberchick: My opinion is that you will NOT have radiation if you had bmx. I had bmx, and my onc was like: No radiation. I said, "none?" He said, "None."  Then, "what is left to radiate?"  But then, I was considered node negative (isolated tumor cells).  If you are positive nodes in some weird circumstances I'm not familiar with I think there could be radiation but I wouldn't think with your small amount ie micromet that would qualify for the general, no radiation needed when there's a bmx.

  • Kimberchick
    Kimberchick Member Posts: 26
    edited May 2011

    Thank you ALL for this information!  I know I need to just visit my oncologist and plan to do that this next week.  But in the meantime, it was just nice to hear from you knowledgeable women!  I appreciate it.

  • lago
    lago Member Posts: 17,186
    edited May 2011

    KSD I'm not saying you aren't IIB, of course you are.  I'm just saying that within each stage there are many definitions. So many people think that stage IIB means you have to have infected nodes.Granted I haven't seen a lot of big tumor no node women. Even my BS was surprised I had no nodes.

    I personally like the staging information on the NCI site here: link 

  • Letlet
    Letlet Member Posts: 1,053
    edited May 2011

    Sorry i did misread the part about estrogen! I'll edit my post. Thanks for pointing it out.

  • Beeb75
    Beeb75 Member Posts: 325
    edited May 2011

    I'm stage 2b too, had bilateral mastectomies and am doing radiation. It was a hard call, but 2 radiation oncologists recommended it mainly because of my young age (35) and high grade of cancer. I'm having radiation to my chest wall only (in other words to my reconstructed breast). Some people also get radiation to the axilla (armpit) and collarbone area.



    Depending on if they do the oncotype test on your tumor, and your age, I think you will be offered chemo and hormonal therapy. Radiation will be a harder call. A lot depends on how aggressive you want to be in your treatment. Will you want to do everything possible to keep it from coming back? Or are you willing to accept some risks to avoid some treatment. Best of luck in your decisions!

  • shells43
    shells43 Member Posts: 1,022
    edited May 2011

    Just chiming in as another 2b with large tumor & no nodes. I had chemo and radiation to the chest wall. The radiation was recommended, but was my choice. At 43, I wanted to do everything possible and not be sorry later that I didn't. By the way, with a tumor my size (9.7 cm x 9.2 cm, the size of a tennis ball) I had a 92% chance of having positive lymph nodes. Even with negative nodes, chemo was decided upon without an Oncotype test. It was not even offered by my onc and I hadn't joined this site yet to find out about it! I don't think the results would have made any difference in the course of my treatment. Just do what is right for you and be at peace with your decision.

  • momand2kids
    momand2kids Member Posts: 1,508
    edited May 2011

    Hi

    I had the same size tumor- was considered 2A and everyone thought I would not need chemo--oncotype came back in the gray area- so I decided on 4 rounds of A/C and radiation (had a lumpectomy)--never regretted it--- feel like I did it all--

    Get your opinions, the oncotype then you will be able to make a decision.  Micromets are not necessarily the issue- but the oncotype can really help you.  For me, the micromets would bother me and I would probably have chemo--- but everyone's level of risk tolerance is different.  

    You will ultimately make the right decision for you once you have your info.

  • badger
    badger Member Posts: 34,614
    edited May 2011

    Hi, I had bilateral mastectomy with sentinel node mapping in Feb 2010.  Was dx stage IIb due to a 2.5 cm tumor in R breast and a micromet in R sentinel node.  The official staging is written as: T2 N1(mi)

    Was offered a choice between chemos (taxotere & cytoxan (TC) or adriamycin & cytoxan plus taxol (AC + T)).  Chose the TC due to a family hx of heart disease, the A can be harder on your heart. I asked about oncotype test but onc said no, as we didn't need it for a tx decision. 

    Did 6 rounds of TC chemo March - June 2010 and been on tamoxifen since July.  I'll be on tamox 5 years total then we'll see what's next.  Yes I lost my hair, two weeks after first infusion, but it came back around Labor Day and is real cute now.

    I did not have axillary dissection, did not have radiation, and did not do reconstruction.

    I try to walk every day, even through chemo, even if all I could do was walk around the block.

    PM me if you want any more info.  Best wishes and big {{hugs}} 

  • voraciousreader
    voraciousreader Member Posts: 7,496
    edited May 2011
    atta woman Badger!!!!!  Laughing
  • BarbaraA
    BarbaraA Member Posts: 7,378
    edited May 2011

    I had a micromet and my MO ordered the Oncotype test which came back low so no chemo for me. I am older, however, at 59.

  • calamtykel
    calamtykel Member Posts: 1,187
    edited May 2011

    judyfams - Lymph node involvement trumps oncotype.     If you have any LN involvement, they will strongly recommend chemo, as the "horse is out of the barn" as they say.... 

    Hang in there - your type responds well to chemo - it's going to be okay.  I just finished chemo in November and honestly, the "waiting" wondering and worrying was far worse than the actual chemo medication! =:O  It can be done and you can do it!

  • sapphirelilac
    sapphirelilac Member Posts: 13
    edited May 2011

    hi

    i think we have the same results. when i had my lumpectomy all lymph nodes were negative, thank God. based on the results my onco told me that all i need is radiation treatment. i had it for 30 days and now i am taking tamoxifen. 

  • CarylC
    CarylC Member Posts: 230
    edited May 2011

    I had a mx and am now doing 6 rounds of TCH, a year of Hercepting, to be followed by radiation.  I don't know for sure if it's because I had macromets in my nodes or extracapsular extensions but my onc said we have one chance to "cure" this and if we don't do it the first time, we are just treating after that so we're doing everything we can.  Period.  

    I figured he knows better than I do so I'm going for it.   I also got 2 opinions from 2 different oncology groups, one from a major teaching hospital and one from a local onc who I chose to be treated by.  Same story from both.

  • IsThisForReal
    IsThisForReal Member Posts: 384
    edited May 2011

    I had a lumpectomy and recieved my full pathology report afterward.  I also had macromets, and the RO strongly recommended rads, and he did the supraclavicular nodes as well.  Before rads, of course, I did 6 rounds of TCH and continued to 18 tx of herceptin.  As CaryIC said, we have one chance at this, and am happy to say I am having my BLM this summer and will then focus on total hystrectomy. 

  • Sherry56
    Sherry56 Member Posts: 6
    edited May 2011

    Hi,

    I also have stage 2/3 and estrogen and progesterone positive, HER2 negative. One lymph node was involved my tumor was 2.5 did have a lumpectomy. Had my first Chemo on Wednesday not so bad, I did have some stomach cramping though with mild headache. But was given drugs to take care of nausea which helps the cramping and headache as well . So all and all feeling ok. Still able to do what I usually do.  Can expect my hair to fall out on next treatment, feel pretty depressed about that. Depression is a problem at times. I don't really have a support system so I just try to suck it up and try not to have my own little pitty party. This might be a long haul. My chemo treatment is 1 time every 3 weeks by iv injection and it takes up at least 3 1/2 hours to start and finish. I will start radiation-5 days a week for  6 weeks in August with Hormonal theraphy later. Good Luck. Sherry 

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