Anyone not have radiation with Triple Negative

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lmcclure4477
lmcclure4477 Member Posts: 180

I am Triple Negative Stage 1A and had a double masectomy about a month ago. Margins were clear no cancer in the lymph nodes. I start chemo Monday but was told I don't need radiation. Anyone else not have radiation??

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Comments

  • Missy123
    Missy123 Member Posts: 18
    edited February 2013

    Hi lmcclure4477,

    I am the same stage as you and also had a double mascectomy.  Based on a number of factors including tumor size, location, no lymph node involvement both my medical oncologist and a radiation oncologist felt that since I had a mascectormy I did not have to have radiation.

  • lmcclure4477
    lmcclure4477 Member Posts: 180
    edited February 2013

    Looks like we had the same diagnosis. It is great to hear someone with a similar diagnosis also didn't need radiation. I start chemo Monday and will be getting the same drugs that you had.

  • Ann360
    Ann360 Member Posts: 15
    edited February 2013

    I have read that you either have a lumpectomy + radiation, or a mastectomy w/o radiation.  Not sure how accurate that is for every case.

  • Missy123
    Missy123 Member Posts: 18
    edited February 2013

    There is some good information on this website regarding when radiation treatment is appropriated:

    www.breastcancer.org/treatment/radiation/when_appropriate

  • Luah
    Luah Member Posts: 1,541
    edited February 2013
  • PeggySull
    PeggySull Member Posts: 686
    edited February 2013

    I won't know if I need radiation until the pathology report comes back from my bilateral mastectomy.



    When in doubt, get a second opinion, maybe from a trusted and knowledgeable radiologist.



    Trust your intuition after you've gathered and assimilated all the info you need.



    Peggy

  • jcolford
    jcolford Member Posts: 120
    edited February 2013

    Hi everyone,

    I am triple negative BRCA1 and I just completed 4 rounds of AC and 4 rounds of Taxol. The radiation oncologist told me that I don't "qualify" for radiation. My tumor was 4.3 cm and I had 3/5 lymph nodes that were positive for cancer. I have had a mastectomy, SLND and ALND. I don't know if I should be fighting for radiation or trust that they know what is best. Any advice?

    Thanks,

    Jo Anne

  • lmcclure4477
    lmcclure4477 Member Posts: 180
    edited February 2013

    jcolford: I would at least get a 2nd opinion. Since it was in lymph nodes and the tumor was pretty big, I would think you would be a candidate for radiation. I am no doctor, but I learned you need to fight for yourself! I was told no radiation for me but I totally trust my surgeon. She even consulted with a radiation oncologist who agreed I didn't need radiation. My tumor was 1 cm and they removed 5 lymph nodes and skeletal tissue that was closest to the cancer and they were all negative for cancer. I am also getting 4 cycles of AC and then 4 cycles of taxol. Started yesterday. Trust your instincts and if u think you should get radiation then get a 2nd opinion.

  • minxie
    minxie Member Posts: 484
    edited February 2013

    I didnt complete radiation and ended up with a local recurrence. No one can say for sure if the rad would have made a difference, but I wish I'd have finished, just to have all my bases covered.

  • Luah
    Luah Member Posts: 1,541
    edited February 2013

    Jo Anne: I would get a second opinion.

  • sheila63
    sheila63 Member Posts: 38
    edited February 2013

    My doctor did not recommend radiation after a double mastectomy, and chemo, and left the decision up to me.  However, when I spoke to my radiologist he stated that radiation would reduce my chances of a local recurrence by 20%.  Since triple negative is such an aggressive disease I wanted to fight it with every weapon available, and decided having the radiation would mean I was doing everything I possibly could. 

    Jo Anne, I agree with Luah, get a second opinion.

  • lmcclure4477
    lmcclure4477 Member Posts: 180
    edited February 2013

    Sheila63: Did u have radiation the first time u were diagnosed? I see that you had a reoccurrence in 2012 (I am so sorry to see that). I often wonder if I will have to go through all of this again.

  • sheila63
    sheila63 Member Posts: 38
    edited February 2013

    Yes, I did have radiation the first time after a lumpectemy.  My doctor recommended me to have a mammogram every six months on the affected breast but yearly on the other.  I wished I had pushed for every six months on both, but little did I know it would come back in the other breast, since the chances were low. 

    Hopefully you will never have to go through this again.  Just know that we are always here for you.

    Hugs,

    Sheila

  • lmcclure4477
    lmcclure4477 Member Posts: 180
    edited February 2013

    Sheila: Did u have radiation the 2nd time when you had your reoccurrence? I was told I don't need radiation because I had a double masectomy and clear margins and lymph nodes. Three different doctors confirmed that they didn't feel I needed it. Just want to make sure I am not making a mistake. This chemo is making me miserable and don't want to go through it again!

  • sheila63
    sheila63 Member Posts: 38
    edited February 2013

    Yes, I did have radiation the 2nd time also.  If you have three doctors confirming that you don't need it,  I would feel safe with that decision.  Neither of my doctors would say yes or no so I made my own decsion.  By you having no postive nodes is definitely a huge plus, and our doctors keep a close eye on us for the first five years. 

     I am so sorry about the chemo making you feel so bad.  There were times when l was just ready to stop, and take my chances, but I knew this was the strongest weapon I had to fight with.   

    Good luck to you, and hang in there, you will do great!

    Hugs,

    Sheila

  • InspiredbyDolce
    InspiredbyDolce Member Posts: 1,181
    edited April 2014

    I did not have radiation, I had 4 rounds of CT for chemo.

    My medical team presented my case to the tumor board, and it was decided I did not need radiation.  About 4 months post-chemo, I discovered, through my own research, that I had a narrow margin.

    I then went out and got 2nd opinions on whether I needed radiation.  I went before a 2nd medical board, and they felt overwhelmingly that there was not enough evidence to support radiation, even though I had a narrow margin.  We also discovered that my surgeon did remove a sliver of muscle at tumor location, and the 2nd independent lab noted that there was a rim of fat around my tumor.  They felt all these variables added to my narrow margin, making it much wider.

    This 2nd board also felt surveillance was best for me, based upon the conditions of the diagnosis, and as for the question of at what point is radiation most effective, they didn't really even address that, as they felt I didn't need it.  So for me, they felt strongly it was best to keep this option available, if I ever needed it, rather than use it upfront without enough elements to warrant it. They said they could give it to me, if I felt 'that strongly' about it, but that they felt pretty confident not to use it.

    I at first felt very aggravated that nobody had told me about my narrow margin, but it looks like both medical teams came up with the same answer - no radiation, in spite of things.  The 2nd opinion, the Radiation Oncologist, said if this was her, she would opt for surveillance.  I felt some sense of relief knowing that I still had that option available.

    But I think with TNBC, you just don't know.  The newest research suggest that there are 4 distinct subtypes of TNBC - some are aggressive, some aren't.  It worries me some days, the thought of a recurrence, and then other times I can go for weeks without worry.  It's just hard to deal with, having a TNBC diagnosis, but I hear it gets easier day by day.  I'm a 1 year survivor. I think I would have worries whether or not I had radiation. 

    In the end, you have to trust your medical team, if your gut feels that they are making the right decisions for you.  If your gut tells you something is not right, seek a 2nd opinion.  Don't feel like they will hold that against you, they know and even come to expect that patients seek additional opinions.  They just want to see you well and healthy, however you get there.

    I'm Type A personality and it was so hard to give up control to my doctors, and not question everything.  I still do that ... but to a lesser degree.  :)

    I wish you all the best with your decisions.

    Many hugs!

    - 2nd opinions / tumor boards / radiation

  • InspiredbyDolce
    InspiredbyDolce Member Posts: 1,181
    edited February 2013

    I want to add, the % reduction from radiation, should be taken into account with what numbers you are starting with.  If someone has a 50% risk of recurrence, and if radiation reduces that 30%, that is a huge deduction.  However if someone has a 10% risk of recurrence, and radiation reduces that 30%, the risk to benefit ratio is different.  So when you are with your Radiation Oncologist, ask for the % as it pertains to your particular case.  That can also help you with your decision.

  • MsBliss
    MsBliss Member Posts: 536
    edited February 2013

    Missy, 

    Did you do the mx after the lumpectomy?

  • Missy123
    Missy123 Member Posts: 18
    edited February 2013

    Yes, I had a lumpectomy first then underwent chemotherapy.  While getting chemo I was tested for the BRCA mutation.  Since I have a mutation of "uncertain significance"  I decided to have a bilateral masectomy. 

  • melissa119
    melissa119 Member Posts: 172
    edited February 2013

    Just to chime in I had BMX with 1.7cm tumor clear margins no positive lymph nodes and had 4dd AC and 12 weekly taxol no radiation. My BS said before my surgery if my tumor was more than around 4cm and/or any positive nodes I would need radiation but luckily I did not. Anyway hope that helps. Joann. I would def get a second opinion.

  • lmcclure4477
    lmcclure4477 Member Posts: 180
    edited February 2013

    I spoke with my breast surgeon again yesterday about needing radiation. She said from my pathology report I did not qualify for radiation with the bilateral masectomy. She reassured me that my pathology report from surgery came back the best that it could and not to worry. She is a great doctor and I really trust her.

  • susan1231
    susan1231 Member Posts: 6
    edited February 2013

    I had BMX no positive lymph nodes 4 cm tumor first go round.  Lymph nodes were only tested on the affected (left) side.    Radiation was not recommended so just chemo.    Recently diagnosed again with much smaller tumor (1.2mm) - discovered during a routine follow-up pet scan.   Since this one was not on the same side as the original tumor it was classified as a "second primary diagnosis" rather than a recurrance.   This time they are having me go thru radiation + chemo.   The pet scan did not show anything in the lymph nodes or anywhere else other than the tumor site, but they are being conservative in case there is a cell still floating about in there.   They are radiating the entire right breast as well as the lymph nodes on that side. 

  • Robyn-6591
    Robyn-6591 Member Posts: 2
    edited February 2013

    Likewise triple negative with stage 1A. Right mastectomy and removal of 12 lymph nodes (clear). Double mastectomy very rarely an option in New Zealand. I have been told radiation isn't of any benefit and I have to decide (no recommendation has been given) whether I want chemo. Suggested regime was cyclophosphamide and doxorubicin followed by paclitaxel. % for and against treatment both looked low and I was put off by the possible long term side effects (leukaemia and/or heart muscle damage). Now been offered cyclophosphamide and docetaxel. Have decided to go with this option and start 11th March.

  • cgabbyj
    cgabbyj Member Posts: 6
    edited April 2013

    I had tnbc, stage 1A, all 3 nodes taken were negative. 3 lumpectomies with fuzzy margins so had a mastectomy which finally yielded clear margins. I was not offered chemotherapy nor radiation since I had no metastasis and my tumor was tiny (>0.5 cm). Later, I found I had a 2nd tiny tumor which was er+/pr+ and was offered tamoxifen but I chose surveillance because tamoxifen's side effects seemed quite awful and would present a barrier to getting into shape. My joints are stiff enough and I struggle with getting enough exercise as it is.

    Glad to be here,

    Cynthia

  • TNmother
    TNmother Member Posts: 11
    edited April 2013

    Hi ladies, iam 38 and was diagnosed with IDC stage 2, grade 3 TN. I had a lumpectomy & clear lymph nodes. Just finished up 4 rounds of a/c and starting 12 rounds of taxol. Can anyone tell me the SE of taxol? Also I'm debating on radiation, dr says yes but not sure why? Thank you for any input!!

  • Luah
    Luah Member Posts: 1,541
    edited April 2013

    TNmother: I found taxol much easier than AC, I felt pretty much felt normal. I had some blackened nails and toe nail loss; a slight rash on my arms; loss of eyelashes and some ankle swelling at the end. But my hair started growing half way through!   

    Radiation is virtually ALWAYS given with a lumpectomy. Stats that show equivalent outcomes Mx versus Lx are based on Lx plus radiation, a standard of care now for over 20 years. And recent evidence suggests that radiation may have special benefit for TNs. See my post above.

    Do you have a medical condition that contra-indicates radiation? 

  • TNmother
    TNmother Member Posts: 11
    edited April 2013

    Luah, no medical condition but afraid it will hurt my heart! It's on my left side & just not sure it's worth the risk? I'm so glad to hear taxol is easier, ac has been rough especially when I have a little boy at home with me!!

  • 3wishes
    3wishes Member Posts: 6
    edited April 2013

    Hi Missy,

    What does uncertain significance mean?

  • Luah
    Luah Member Posts: 1,541
    edited April 2013

    TNmother: Bring your concerns to your RO. Ask about the risks and benefits (i.e. potential for long-term SEs from rads versus survival outcomes of Lx without rads). Ask to see research findings, and how he will avoid your heart, etc.

    Many, many, many women undergo rads on the left side (I was one of them) and suffer no ill effects. However, I had the same concerns and my RO took me over to a computer monitor and showed me precisely where the rads would be hitting. 

  • russem
    russem Member Posts: 11
    edited April 2013

    I'm another one that didn't get radiation. They felt that at this point I didn't need it. I'm now six months out from my last chemo.

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