Chemo types

Merilee
Merilee Member Posts: 3,047

What kind of Chemo have you ladies with ILC had? And why did your oncs choose that particular type?

Comments

  • karen1956
    karen1956 Member Posts: 6,503
    edited December 2009

    TAC chemo - every 3 weeks...6 rounds......

    I was in a clinical trial.....other options for the trial were AC + Taxol (4 rounds each every 2 weeks), or AC + Taxol and Gemzar (I think the Gemzar was with the Taxol, but other wise same as just AC + T).  Assignment was randomized.

  • dlb823
    dlb823 Member Posts: 9,430
    edited December 2009

    Merilee ~  I had Taxotere & Cytoxan for multicentric ILC with same hormone stats as yours.  PM me if you'd like a link to an excellent current UCLA video that explains the history of chemo for breast cancer, where we are today with targeted therapies, and why some are more beneficial than others for certain types of bc.     Deanna  

    P.S.  I went to 3 oncs who all had different recommendations -- AC+T, TC & no chemo!  I chose UCLA b'cuz it was clear that they really knew their stuff and I had complete confidence in them.

  • AnacortesGirl
    AnacortesGirl Member Posts: 1,758
    edited December 2009

    Merilee,

    I am on a trial through Seattle Cancer Care.  The first 12 weeks were a combination of Taxol and Sutent (sinutibin) and the current chemo is 15 weeks of AC.  Initially I saw two oncs and they both wanted to do neoadjunvant because of the multiple tumors and the lymph node mass under my arm.  The cancer had change quickly in the last month since I initially felt pain and went for a screening mammo so they wanted to take the systemic approach first.  The Sutent is similiar to Avastin in that it attacks the vascular support to the cancer.  The overall goal is to kill anything that might have made it to the lymph nodes and beyond and then get a good reduction on the tumors in the breast for clear margins when I have the mast.

    dlb823,

    Can you post that link?  I would like to learn more about the targeted therapies.

  • dlb823
    dlb823 Member Posts: 9,430
    edited December 2009

    Christy ~  I just PM'd you that link.   Deanna

  • pickle
    pickle Member Posts: 1,409
    edited December 2009

    I had 2 tumors totalling 4.6 cm. IDC and ILC. Stage 2 grade 3 er/pr + her2-. node neg. Treatment was mastectomy, 4xAC. Tamoxifen

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited December 2009

    I am having TCH x 6 followed by radiation and herceptin. The only reason I'm having chemo is because it was HER2+. If it had been HER2 -ve, then radiation was the treatment not chemo. If you were hormone receptor negative and HER2 -ve ie triple negative, then chemo is the only option. If you are stage 1 node negative but hormone receptive, then you shouldn't be having chemo at all.

  • Texas357
    Texas357 Member Posts: 1,552
    edited December 2009

    I had 3 rounds of 5FU/Epirubicen and Doxitaxel followed by 9 rounds of taxotere. I'm now on Femara. I think oncologists choose whatever has worked effectively for their patients. As my oncologist explained it, "we each have our own blend of potions".

  • Gitane
    Gitane Member Posts: 1,885
    edited December 2009

    I had 6 rounds of dose dense AC, four of them before the mastectomy and 2 after.

  • cammy2
    cammy2 Member Posts: 42
    edited December 2009

    I will start in Jan with AC every three weeks for four cycles and then Taxol weekly for 12 weeks, then Hormone therapy. Is there an area here that talks about side effects ladies have had from the different combos of chemo?  I have heard the Adriamycin is really tough and then someone else said taxol was the worst for them.??

    Still recovering from the bi-lat mx on Nov 20th.  Had three seroma drainings - may need one more.  Going well except the nerve pain - i wasn't prepared for how crazy the nerves have reacted.

  • amlg1
    amlg1 Member Posts: 596
    edited December 2009

    I had dose dense of A/C every 2 weeks x4, then dose dense Taxol and Herceptin every 2 weeks x 4,I have to do herceptin for 1 year every 3 weeks.Everyone reacts different to chemo,with all the anti nausea meds given,I did very well.It was so tolerable for me.

  • Gitane
    Gitane Member Posts: 1,885
    edited December 2009

    cammy2, I am sure there is lots of discussion about SE's on the chemo thread, and probably elsewhere.  Hopefully someone who knows this site better can help.  You could try the "search" feature, too.  Sorry to hear that you have had the seroma problems after your bilat.  And nerve pain!  Are you getting help with that, exercises, heat/cold, meds?  Our bodies sure get beat up through all of this.   I had AC every two weeks so I could maybe help with that, but never had Taxol.  For me the biggest SE (not including hair loss, of course) was major fatigue and mild nausea.  I slept a lot, and didn't feel up to eating very much.  I remember crying all the time, which my chemo nurse said was partly due to the decadron.  It hyped me up, then I'd emotionally crash afterward.  Well, it was probably also me not handling this whole thing too well, either.  I enjoyed soups and toast, crackers, mild juices, and cooked veggies.  Once I started taking Kytril, about half way through treatment,  most of the nausea issues eased up.  The effects for me were cumulative, so that by the end I was really zonked!  I ended up getting shingles, which was treated and cleared up. Towards the end of treatment I got mouth sores, but it was also treatable.  I had a great response to chemo and I know many ILC women do.  

  • Pt0121
    Pt0121 Member Posts: 4
    edited April 2010

    I wondered about the chemo too.  What about adriamyacin and cytoxin?  Any of you have them? I am suppose to put port tomorrow.  Start chemo in a wk or two.  Still wondering if i am doing the right thing.

  • momand2kids
    momand2kids Member Posts: 1,508
    edited April 2010

    pt

    I had AC-- 4 rounds delivered over 8 weeks.  I was able to work for the most part- and I have young children--- I was usually out of commission for about 3 days each time-not sick but queasy and not really feeling up to myself.

    I am over a year out of chemo (finished on 2/27/09) and almost a year from radiation (finished 5/6/09) and I feel GREAT!!!   it does knock you down, but you will get back up.....

     why are you wondering? did you have an oncotype test?  You should really do what you feel is necessary--I did not want to do chemo but I could see that there would be a benefit for me.... my recurrence rate dropped from about 15% to 8% (or something like that).   

    I had a strong and healthy heart going in and  was in excellent health otherwise, so I feel like I tolerated it well..... but as has been said, everyone has different side effects.

    Happy to give more info if you need it.   

  • hopeinfitcher
    hopeinfitcher Member Posts: 92
    edited April 2010
    I had:Cytoxan/taxotere,6 weeks-every 3 weeks,after-35 radiation,after-5 yers-Arimidex.
  • 070Maria
    070Maria Member Posts: 4
    edited October 2010

    Treatment mastectomy, currently AC

  • cathmg
    cathmg Member Posts: 278
    edited October 2010

    Hi,

    I had TC, 4 rounds, in the fall of 2008. As a matter of fact, my last treatment was on Halloween, so I never forget that date. My onc said that TC was a newish treatment for the type of cancer I had, and seemed  to be giving better results. I was glad to skip the Adriamycin.

    Best, 

    Cathmg

Categories