What the norm for chemo with TNC?

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debbiej
debbiej Member Posts: 72

I was just wondering if everyone with TNC is on pretty much the same chemo regiman?  I start Chemo on Tues. and he has me on 12 wks of Paclitaxel (taxol)  The 12 wks of Fluorouracil,Doxorubicin, cyclophosphamide.  Does this sound like the right course of action?  Has this combination worked for anyone else.  Thanks, Debbie

Comments

  • Titan
    Titan Member Posts: 2,956
    edited January 2013

    I had dose dense ac and t.....ac 4 times every two weeks, then 4 taxol...sounds like your onc is giving you the maximum..which is a good thing...good luck to you!

  • gillyone
    gillyone Member Posts: 1,727
    edited January 2013

    Where do you live Debbie? Yours looks like FEC/T which seems more common in Europe and Canada. Like Titan I had dose dense AC/T.

  • Renae64
    Renae64 Member Posts: 99
    edited January 2013

    I had 3 months AC and 3 months taxotere. Just a question, have your doctors given you a bone scan? I had clear nodes, but bone mets occurred! Anyone else out there like me? Are bone scans done with TNBC cuz it is so aggressive, please help. Hugs, Renae

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

    Debbie: FEC/T is pretty common (and considered equivalent to AC/T)... good that your onc is doing the taxol first. There have been some recent studies showing that doing the taxane first has better results. 

  • tisthyme
    tisthyme Member Posts: 49
    edited January 2013

    Debbie, I had 12 weekly taxol and then 4 AC, every 3 weeks.  I am curious why you are doing 12 weekly FAC. I have heard it is best to do smaller amounts of chemo closer together, rather than a large amount at a time spaced farther apart, but have not heard of anyone doing 12 weekly FAC.  I am curious to why you are doing FAC, FEC is usually more common.  Most TNs I know of had the AC part (Doxorubicin, Cyclophosphamide), but not the F (Fluorouracil), and if they had the F it was FEC not FAC.  

    Renae64, I had a pet scan and a bone scan. The reason for the PET was they were trying to stage me prior to beginning neoadjuvant chemo, and when a place lit up on my back, they did a bone scan to figure out if it was a bone met or arthritis.  Thankfully, it was shown to be arthritis.  I know many TNs who do not get staging scans of any kind, unless they have an affected node or other concerns.  Insurance doesn't seem to want to pay for these scans unless they believe it is warranted.

  • debbiej
    debbiej Member Posts: 72
    edited January 2013

    I will try to answer all your questions, but I am not to great with the abbreviations yet.  I live in Texas and go to what is considered the best in the country clinic, md anderson, mays clinic.  I will take taxol once a week for 12 weeks, then the other combination of drugs that I mentioned on my original post every three weeks for a total of 12 weeks, than I believe I would do 6wks of radiation.  I have not had a bone scan.  It has been two months since my pet scan and the only thing that showed up then was the lung nodule.  At first doc thought he might do another pet but then decided to go ahead and start chemo saying that no matter what it showed we would start chemo anyway and also thought it would not show anything in two months time.  Does anyone know about that?  Can TNC grow another tumor in 2months time?  He was also considering doing another mammo with ultra sound on breast with the lumpectomy but decided against that as well.  He was pretty undecided which may me a little uncomfortable.  My husband would question him on why he wanted to do them again and that's when he would say, you're right it to soon and probably wouldn't show anything.  I wish my hubby would of just keep quiet, although I didn't tell him that, and let the doc make up his own mind.  Also I thought there would be a group of ONC putting thier heads together to decide which was the best course of action to take but that didn't happen either just him.  I am going to email the doc this morning and see about that.  I was told by a good friend of mine that's the way things are handled there.  She has a very rare skin cancer on her face.  She said they would sit in front of her and discuss thier game plan.  So I was somewhat disappointed it was just this one guy.  Doc was also not happy with the margins on my lumpectomy and said they may have to in at a latter date and explore again.  Not happy about that.  I hope I have answered all your questions so you can give me a little more information.  Doc did say that Taxol would be the easier of the two.  Hugs to all of you, you are great friends, Debbie

  • JoanQuilts
    JoanQuilts Member Posts: 633
    edited January 2013

    I am triple negative and had six treatments of taxotere and cytoxan three weeks apart. Sometimes treatment differs by where you Sre in the country. Also I had a ver small tumor no Lvi and neg nodes.

  • marywh
    marywh Member Posts: 2,280
    edited January 2013

    Hi Debbie did you get my pm's? been thinking about you. The way it worked with me is that they would all sit around and talk about me in their morning meeting and then my onc. would see me by himself. I think your question about a new tumor growing back in 2 months is a million dollar question. This is a sneaky little buggar we're all dealing with. Going back in to check margins, I know its a pain, but it really is better to be safe than sorry, considering the alternative.

  • tisthyme
    tisthyme Member Posts: 49
    edited January 2013

    Oh ok, you are doing the FAC every 3 weeks.  I live in Corpus Christi and followed the MDA protocol for TNBC.  at that time (July 2011), it was 12 weeks of Taxol, then 4 rounds of AC every 3 weeks.  Most TNs I knew where doing Dose Dense AC, meaning AC every 2 weeks instead of every 3, so I asked my Oncologist if I could do dose dense.  She said that we are following the MDA protocol and that places that follow Dana Farber or Sloan Kettering protocol are doing dose dense. Yes the weekly Taxol was far easier for me.  I had 33 radiation treatments and that was easy for me; the driving to radiation everyday seemed to be the biggest pain about it.

    About your question: Can TNC grow another tumor in 2 months time.  From what I have read and heard from TN sisters, yes, oh yes it can.  TN seems to be one of the fastest growing. SOme women say that between mammogram and surgery (about 1 month) their tumor doubled in size.  Although it is one of the fastest growing with rapidly dividing cells, it is also usually quite responsive to chemo.  Most chemo works on killing rapidly dividing cells and that is just what we have.

    Debbie, I also suggest that if there is anything you are uncomfortable with, speak up! get a second opinion! You have to be your own advocate, the squeaky wheel gets the oil. Don't be afraid of speaking your mind, ask your drs what they would suggest for their loved ones.  Our health care is only as good as our weakest link.  Don't let that be YOU! Good luck to you.  Wishing you a complete response from chemo and few side effects.  

  • debbiej
    debbiej Member Posts: 72
    edited January 2013

    Thanks, that is exactly what I did, I just got done typing a long email to the doc expressing my fears and opinions.  Hopefully I went about it tactfully and didn't offend him.  I am not a shy person when it comes to my children, I know that is funny thing to say right now in this situation but, what hurts them hurts me, and this is killing them, so I will stick up for myself to infinity and beyond!  Just like our friend Buzz! LOL! 

    Thanks girls, for your never ending support! 

    Lots and lots of hugs!  Debbie

  • deeteeone
    deeteeone Member Posts: 19
    edited January 2013

    I had 4 rounds of AC..then I just finished 33 rads..It feels sort of odd not having a saftey net anymore.

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

    Almy: We have all gone through those terrors about spread - very natural and very scary! You're doing chemo - that's a good thing, a systemic treatment that can hopefully reduce your tumour and catch any rogue cells that may be circulating. It sounds like you are in very good hands at the Mayo, and the treatment plan makes perfect sense. Try not to worry. 

  • sheila63
    sheila63 Member Posts: 38
    edited January 2013

    I had ACT for 12 weeks, except the last week I could not take the taxol since I was accumulating so much fluid.  I am hoping this does not make a difference.  Good luck!

  • Denisehfred
    Denisehfred Member Posts: 4
    edited February 2013

    Has anyone tried the treatment IPTLD:Insulin Potentiation Targeted Low Dose

    http://www.bestanswerforcancer.org/what-is-insulin-potentiation-therapy-low-dose-iptld/

    for TNBC?  If so, I was wondering if you could tell me your experience.  Thank you.  

  • HollyHopes
    HollyHopes Member Posts: 497
    edited February 2013

    I had dose dense (every other week) A/C 4x followed by dose dense Taxol 4x and then 35 rads...

  • Nuan
    Nuan Member Posts: 19
    edited February 2013

    I had 4 rounds of TC then 30 radiations, including 5 boosts.

  • slv58
    slv58 Member Posts: 1,216
    edited February 2013

    Hi, I'm having 6 FEC-T every 3 weeks but when I see my oncologist on wed. I'm going to ak about dose dense. I also see most women are getting AC,so I'm wondering about that as well. Any advise ?

    Dx 1/21/2013, IDC, 3cm, Stage II, Grade 3, ER-/PR-, HER2-Chemotherapy 01/23/2013 Cytoxan, Ellence, fluorouracil, Taxotere
  • InspiredbyDolce
    InspiredbyDolce Member Posts: 1,181
    edited March 2013

    I think the dose / regimen is also determined by other factors in the path report, family history of bc, micromet of lvi concerns, etc.  

    My treatment consisted of 4 cycles of Cytoxan and Taxotere, every 3 weeks, and at a 60% higher dosage than that which is listed in the NCCN guidelines.  

    I had a BMX, the bc was only in one breast, at one spot.  Nothing abnormal in the other breast. 

    I did not have radiation.  

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

    That ITPLD sounds exciting - I have not heard of it on these boards to be a common treatment, but you can place it in the seach criteria and see if there are conversations about it.  That should be a reminder to us to try to limit our sugar!

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

    Because some research correlates high fat diet and sugar to TNBC, you would think they would add this to the TNBC regimen as an additional medicine in the infusions.

  • Missy123
    Missy123 Member Posts: 18
    edited February 2013

    Hi Debbie,

    My chemo consisted of 4 rounds of Adriamycin and Cytoxen every 2 weeks, then 12 weekly sessions of Taxol.  If you have questions about the chemo your doctor is prescribing you could always get a second opinion.  However you are being treated at an excellent facility so I'm sure the chemo they are recommending is appropriate.  Hope everything goes well with your treatment and the side effects are minimal.  I found the weekly taxol to be easily tolerated.  I was able to work, though at somewhat reduced hours, during this time.

  • shadytrake
    shadytrake Member Posts: 142
    edited February 2013

    Hi Dolce,

    I'm getting the same chemo as you had plus radiation.  I was surprised that they didn't recommend the ACT grouping but my MO said if my tumor had been bigger, then he would have recommended.  I'm in the "grey" area.  I guess we'll see how it goes.

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

    slv58: FEC-D is equivalent to AC-T and a very common regimen in countries other than the US. It is the big guns, though is "E" is gentler on the heart than "A." I had a long conversation about my onc about this, as I wanted to do dose dense for TN. She had no issue, but it was a bit unusual at the time, and perhaps still is in Canada. To my knowledge there has been no head-to-head study of triweekly FEC-D versus dd AC-T.    

  • PeggySull
    PeggySull Member Posts: 686
    edited February 2013

    Dose dense is the standard treatment for triple negative. I read in Patricia Prijatel's book, Surviving triple negative breast cancer, that if your doc doesn't suggest dose dense you should get a second opinion.



    Peggy

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

    To my knowledge, there is not one standard treatment for TNBC, such as the case in point of "dose dense."  If you open up the NCCN Guidelines Manual, there is not a reference of it in there.  Also, this is one of those things that is up for debate, as it depends on if someone is high risk, and stage of BC.  Not all Oncologists recommend the most aggressive treatment if they believe another treatment would be just as effective without the risks. I think anyone mentioning dose dense as a standard is really putting themselves out there on a limb, unless they are an MD making that statement. Each person comes to the table with a whole set is circumstances and must be evaluated and treated not only due to guidelines but also to personal direct risk factors.  Family history, stage, location, age, health, risk factors, etc are analyzed when a treatment plan is presented to the patient. 

    I had dose-intensified treatment, which was CT treatment every 3 weeks, but at a 60% higher dosage.

    Now - Per the NCCN guidelines, for the characteristics of TNBC that I had, regarding my path report, here is what was referenced for the Preferred Adjuvant Regimens - as you can see, they referenced four different acceptable protocols for the category/stage/etc that my pathology report referenced.  

    So these aren't for other stages/other types, etc.  This one excerpt below, is for treating TNBC according to what was in my pathology report.

    It also includes dosing recommendations in this manual as well.  That's something we don't hear about on these boards a lot, is what dosage did everybody have. 

    From page 44 of the NCCN guidelines, version dated:  7/11/2012:

    ADJUVANT CHEMOTHERAPY1,2,3,4,5

    Non-trastuzumab Containing Regimens (all Category 1)

    Preferred Adjuvant Regimens:

                      ·  TAC (docetaxel/doxorubicin/cyclophosphamide)

                      ·  Dose-dense AC (doxorubicin/cyclophosphamide) followed by paclitaxel every 2 weeks

                      ·  AC (doxorubicin/cyclophosphamide) followed by weekly paclitaxel

                      ·  TC (docetaxel and cyclophosphamide) 

  • anamerty
    anamerty Member Posts: 195
    edited February 2013
  • Ahicks62
    Ahicks62 Member Posts: 19
    edited July 2013

    I had Cytoxan and Taxotere, 4 rounds 3 weeks apart. My oncologist felt this would be sufficient based on my situation, it was a small tumor and no spread to the nodes.

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