TNBC to start chemo next week

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jenkwa2
jenkwa2 Member Posts: 11

Hi everyone

I am new to this forum.I am newly diagnoised with IDC 4cm stage 3 TNBC.My Oncologist reccommended AC every two weeks  times 4 cycles then Taxol every week times 12 weeks.I will receive Neulasta 24 hrs after each chemo treatment.2-3weeks afterchemo  my oncologist said I would have surgery for the remaining tumor that is left.

I receive my port and first dose of chemo on the same day this week coming (week of  Feb. 7th).

 Has anyone had this chemo regimen?

I have been accessing websites regarding the type of treatment I will be receiving,diets I should follow after each treatment due to the possiblity of nausea and type of diet during the duration of my treatment.

Is there any particular foods after each treatment or during the duration of treament anyone followed that worked?

I read keeping ice chips in your mouth during treament may cut back on mouth sores did this work for anyone?

My Oncologist said some patients ate ice cream during their adminstration of chemo  and that help some patients

I have already shave my hair off I did not want to wait to see clumps of hair on my pillow or in the shower.'

If anyone has advice/input I would appreciate it

Comments

  • Titan
    Titan Member Posts: 2,956
    edited February 2011

    Hi jenkwa2!   Good luck with your first chemo...sounds like you are trying to educate yourself prior to chemo and that is a good thing.

    For alot of information go to the Chemotherapy thread on here...you will probably even find a group of women that you can talk to starting chemo in February also.

    Good luck and let us know how you are doing!

  • Sugar77
    Sugar77 Member Posts: 2,138
    edited February 2011

    Jenkwa2 - there is also a really good thread that Titan (posted above) started called "Calling all TNS" On that thread, you'll meet lots of lades with Triple Negative.

  • minxie
    minxie Member Posts: 484
    edited February 2011

    I had that exact chemo regimen. I never got mouth sores. Howevere I made a decision to eat super healthy and cut out all fats from my diet which kind of backfired during the chemo - I dropped 20 lbs and they were concerned about such a drastic weight loss. At the end I started going back to eating whatever could fatten me up, even ice cream. I know some women gain weight on chemo, but I'm thinking it's the ones who need steroids from the Taxol, which I didn't.

    They will give you meds that help with the nausea. For me, the AC was rough, but at the end of the two weeks I'd feel OK. The Taxol weekly though had a cumulative effect, with increasing neuropathy and fatigue each time. My hair did start growing back 1/2 way through though!

    Good luck and let me know if theres anything else!

  • jenn3
    jenn3 Member Posts: 3,316
    edited February 2011

    I did AC, but 12 weekly Taxol treatments. 

    It sounds like you're doing a great job of getting prepared for your 1st chemo.  I did suck on ice chips during the Adriamycin portion of the chemo and I did get mouth sores, not sure if they would have been worse otherwise.  Also, not sure if you've read this or not, but hydrate, hydrate, hydrate before, during and after chemo - it really does help.  Also, if you feel a strange sinus or pressure headache coming on during the Cytoxan push, ask them to slow down them chemo to 45 - 1 hour and the headache should disappear (if you get one). Chemo also seems to cause your mucus membranes to dry out - you may experience a dry mouth or sinuses.  Use Biotene toothpaste and mouthwash, it's meant for dry mouth.  If your nose is dry - use a saline mist - it really helps.   As for the food, I think a lot of us start off with the best of intentions, but in all honesty, your taste buds are affected by the chemo and you'll have good and bad days - eat what you can tolerate or taste and worry about the weight or the "right" thing later. 

    Not sure if you want to do this or not, but I brought a chemo bag with me to chemo and I put things like disinfectant wipes, lifesavers, small soft fleece blanket, fuzzy socks, notebook and pen, crackers and/or a piece of fruit, bottle of water (even though they had water and snacks) and a magazine or book.  That way I had my "comfort" things with me during chemo.  I always put my soft fleece blanket under their blankets and used the rest of what I brought as needed.

    (((hugs)))) I'm sorry you had to find your way here, but it is doable.

  • husbandoftripleneg
    husbandoftripleneg Member Posts: 1
    edited February 2011

    Hi,

    I'm new to this forum but I've been on TNBC foundationsite and Inspire - advanced Breast cancer site for over 2 years. My wife has met TNBC. Please read this recent posting from TNBC site and show to your oncologist.

    "Chemotherapy Sequence Affects Early Breast Cancer Outcomes

    Elsevier Global Medical News. 2011 Jan 7, B Jancin

    SAN ANTONIO (EGMN) - The sequence in which paclitaxel and anthracyclines are given for treatment of early breast cancer makes a big difference in long-term outcomes.

    That's the conclusion reached in what is believed to be the largest-ever retrospective study of the clinical impact of the sequencing of taxanes and anthracyclines. The study involved 3,010 early breast cancer patients who were treated during 1994-2009 and entered into the prospective online database at the University of Texas M.D. Anderson Cancer Center, Houston.

    The clear winner was paclitaxel, followed by anthracycline-based therapy with 5-fluorouracil, doxorubicin (Adriamycin), and cyclophosphamide or 5-fluorouracil, epirubicin, and cyclophosphamide, Dr. Ricardo H. Alvarez reported at the San Antonio Breast Cancer Symposium.

    Starting with paclitaxel rather than an anthracycline-first regimen led to better long-term results in the settings of adjuvant chemotherapy and primary systemic (or neoadjuvant) therapy.

    The adjuvant chemotherapy analysis included 1,596 women, three-quarters of whom received paclitaxel followed by anthracyclines. The 5-year relapse-free survival rate with this regimen was 88.8%, compared with 79.5% when anthracyclines were followed by paclitaxel. The 10-year relapse-free survival rates were 81.8% and 73.5%, respectively.

    Five-year overall survival was 93.1% with paclitaxel followed by anthracyclines, compared with 83.2% for the reverse. The 10-year overall survival rates were 83.9% and 65.6%, respectively.

    In a multivariate analysis that was stratified for potential confounders, including age, clinical stage, hormone receptor status, tumor grade, and era of diagnosis, the anthracyclines-first sequence was associated with a 67% increased risk of relapse (P less than .0001) and a 2.5-fold greater risk of mortality (P = .001), according to Dr. Alvarez, a medical oncologist at M.D. Anderson.

    Among 1,414 patients who underwent neoadjuvant therapy, the 5-year relapse-free survival rate was 79.0% with the paclitaxel-first regimen vs. 61.2% with the anthracyclines-first regimen. Ten-year relapse-free survival occurred in 61.7% and 50.5%, respectively, of these patients.

    Overall survival was 84.2% and 66.2% at 5 and 10 years, respectively, in patients who received paclitaxel followed by anthracyclines, compared with 71.3% and 53.4% in those who got anthracyclines first.

    In a multivariate analysis, the anthracyclines-followed-by-paclitaxel sequence of neoadjuvant chemotherapy was associated with an adjusted 49% higher risk of relapse (P = .01) and a nonsignificant 28% increase in risk of all-cause mortality (P = .17), compared with the paclitaxel-first strategy.

    The mechanism that accounts for the increased efficacy of taxane-first regimens for treatment of breast cancer is unclear, according to Dr. Alvarez."

    I hope this info is helpful. This is usually the opposite way the chemo is given.

    John

  • jenkwa2
    jenkwa2 Member Posts: 11
    edited February 2011

    Thanks everyone for your advice and words of encouragment.I made it through my second round of chemo this week.I am counting down each treatment 2 more treatments of ac then 12 weeks of Taxol.I really am greatful for this site there are different areas for different questions you may have I think its great .Especailly in the beginning when you don't know what to expect.Thanks again.

     Wanda

  • Suze35
    Suze35 Member Posts: 1,045
    edited March 2011

    Bump for lilylady

  • lilylady
    lilylady Member Posts: 1,079
    edited March 2011

    Got it-thanks. Added to Favs. Also went to the TNBC website. That study caused a big stir over there because the ladies who had already started resented that someone would post something that they thought meant they weren't getting the best possible treatment ect.

  • dawn31337
    dawn31337 Member Posts: 307
    edited March 2011

    I found the TNBC site to be somewhat negative.  I don't bother with it anymore.  Sorry I didn't see this thread earlier.  

    I had DD ACx4 and DD Tx4.  I wanted to get this done with ASAP.  Evidently there are no studies that compare 12 weekly T and 4 DD, which I find hard to believe.

    I sailed right through it and was queasy literally 2 or 3 times.  I did have bone pain with Taxol and Neulasta 2 out of 3 times.  I didn't get the shot after my last T and have a follow up next week to make sure my white blood cells are back to normal.  

    Happy to say I am just over 2 weeks past my last chemo, and I feel terriffic!!  Now if I could just grow my hair faster!!

    Best of luck to you, and I hope you have an experience as good as mine was. 

  • Titan
    Titan Member Posts: 2,956
    edited March 2011

    Well..that sucks..I had Ac first then Taxol..oh well..can't do anything about it now..the nurse said that with the AC they were bringing out the big guns first..I'll have to ask my onc about that...I'm not upset about it..but dang..my onc did say that there are changes all the time so I guess this is to be expected..they were doing what was right for then..even though it wasn't even 2 years ago!

    A friend of mine had 4 ac's only..no taxol at all..she is almost 7 years out and doing fine

  • jenkwa2
    jenkwa2 Member Posts: 11
    edited March 2011

    Hi everyone

    does anyone know about purchasing hospital or supplemental indemnity insurance once you have been diagnosed? Aflac doesnot unless you are cancer free fro 10years?if anyone knows or can direct me I would appreciate it

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