Which Chemo drugs used?

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Noranelly
Noranelly Member Posts: 30

Hi I have recently been diagnosed with her2 positive bc. I was just wondering which combination of drugs people have had or are having to treat this cancer? My sister has been having chemo to ,but she had a hormone positive cancer which was very big with 17 lymph nodes involved. Mine was 2.8 cm with 5 positive nodes my oncologist is recommending the same chemo, fec and tax oater but I follow mine up with herceptin. Is this other peeps experience? It seems a bit strange as they are different cancers. Start my chemo 31st October. Noranelly

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  • RebzAmy
    RebzAmy Member Posts: 322
    edited October 2012

    Hi Noranelly

    I also had a similar diagnosis to you and my treatment was as you've described above so in answer to your question, yes, this was my experience - your sister has hormonal breast cancer which is different to yours which is not hormonal but is HER2+ hence the Hercepti.

    Good luck for 31st Oct.

    RebzAmy

  • RoulaG
    RoulaG Member Posts: 239
    edited October 2012

    Hello Noranelly



    I had 6 TCH (taxotere, carboplatin and herceptin), and I continue the herceptin until I finish up 12 months.

  • maryannecb
    maryannecb Member Posts: 1,453
    edited October 2012

    FAC, then Taxotere/herceptin then herceptin alone to complete a year

  • bluedasher
    bluedasher Member Posts: 1,203
    edited October 2012

    Most common in the US for Herceptin positive (regardless of hormone status, stage I through III) is either AC-TH or TCH.

    AC-TH is 4 rounds of Adriamycin and Cytoxan followed by four rounds of Taxotere and Hereceptin then Herception continued to complete a year on it.

    TCH is 6 rounds of Taxotere, Carboplatin and Herceptin then Herceptin continued to complete a year.

    Some doctors use Cytoxan is used instead of Carboplatin and sometimes Taxol is used instead of Taxotere.

    AC-TH has been studied the most and is very effective but there is a small risk of long term decreased heart function and a very small risk of Leukhemia. TCH was compared to AC-TH in a large study BCIRG 006 - heart issues are less common with it and the heart recovers once the Herceptin is stopped and it doesn't have the Leukhemia risk. There was no statistically significant difference in recurrence between the two treatments. It is debatable whether the slightly better but not statistically significant recurrence with AC-TH outweighs the higher side effect risks with it or not and both chemos get used.

    The cancer that they have located has been removed by surgery. Chemo needs to kill any stray cells that are wandering around so the number of nodes involved doesn't make much difference to the type of chemo. They need to treat the type of cell. There is some work going on to see if a lighter chemo will be good enough for early Stage I - node negative tumors less than a centimeter.

  • marjie
    marjie Member Posts: 1,134
    edited October 2012

    I had FEC then Docetaxol(taxotere) followed by Herceptin for 1 year.

  • Terry71
    Terry71 Member Posts: 293
    edited October 2012

    I had the exact same treatment as marjie FEC-D The FEC is fluorouracil, epirubicin, (RED DEVIL)  and cyclophosphamide, and the D- Docetaxol.... I  just finished my herceptin Sept 27th...... had follow up app yesterday, says all is well and see me in 6 months......

  • Noranelly
    Noranelly Member Posts: 30
    edited November 2012

    Great news hope all continues to go well. I have just had first chemo and although I didn't like it I have managed to keep well. Any tips on how u coped with side effects etc as we have exactly the same chemo regime? Noranelly

  • marjie
    marjie Member Posts: 1,134
    edited November 2012

    Noranelly - keep us posted on what your side effects are.  Everyone is different.  One of the most important things is to try and avoid mouth sores!!!  I rinsed my mouth with soda water every time I was in the washroom and I never had a single mouth sore.

    You will learn to know your "cycle" - keep track of your temperature, drink lots and lots of water, rest when you need it, and stay positive ... seems like a long road ahead of you but it will be done before you know it (I used to hate it when people said that to me but they were right!).  Happy to help you anytime.....you are welcome to PM for info if you are more comfortable that way Smile

  • IWILLMAKEITTHRU
    IWILLMAKEITTHRU Member Posts: 4
    edited November 2012

    Hi. Am new to the boards, but have been reading several and find them very helpful. I was diagnosed with Her2+, Stage 3 cancer in Dec of 2011. Had sentinol node biopsy done, removed 10 nodes, 9 were cancerous. The tumor was at the base of the left breast and on the chest wall. Had a mastectomy, and started AC treatments. After 2 treatments I had severe reactions to the chemo. Turned neutropenic, had blood clot that went to foot and am still not able to walk on it, 7 months later. (Almost had to have it amputated.) Also ended up with a pulmonary embolism, pneumonia, and was within minutes of not making it. Spent 25 days in hospital on IV's. Also ended up with a fistula, and colostomy. All caused by the Adriamycin/Cytoxin. So, I cannot have chemo ever!! I have had 5.5 wks of radiation,and am on my 7th (out of 17) Herceptin treatments. I cannot have the taxol that is usually given with the Herceptin. I was wondering if anyone else has had just the Herceptin with no other drug for this type of cancer? If so, how far out from treatments are you?  I actually feel much better now, and am just very thankful to be here to even ask for help..Thanks for any info.

  • Noranelly
    Noranelly Member Posts: 30
    edited November 2012

    Gosh what an awful time u have had. I am sorry to hear of all you have been through. It sounds like words can't describe it! You r doing better now and to get throu that u must have been strong. It sounds like chemo is not for u!!! I haven't had an experience like u but I hate feeling sick etc after chemo and I am not looking forward to my next one anyway take care noranelly

  • Alicethecat
    Alicethecat Member Posts: 535
    edited November 2012

    Hi I Will Make It Thru

    Sorry to hear you've gone through so much re the chemo, sepsis and blood clots.

    I got sepis after my first infusion of FEC (fluoroucil, epirubicin and cyclophosphamide) - treated in ER and hospital admission with IV antibiotics.

    Then I developed small blood clots to the lungs on Taxotere and had other side-effects (peeling skin and low white blood count.)

    The blood clots were treated by injections of Tinzaparin and five-day injections of Lenagrastim. Then I was switched to warfarin, which I am still on.

    I do understand a little about what you've been going through and you have my sympathy!

    However, after my oncologist reduced my dose of Taxotere to 80% of the standard dose, my life turned around and the side-effects went down....

    Is this something your oncologist is likely to do in case you need chemo again or is it too risky for you?

    On the positive side, I was cancer-free after the mastectomy and that's still the same situation eight months down the track after the chemo and radiation and an on-going course of Herceptin so...best of luck!

    Best wishes

    Alice

  • IWILLMAKEITTHRU
    IWILLMAKEITTHRU Member Posts: 4
    edited November 2012

    Thank you for your reply, and good wishes. No, I cannot have any chemo.My white blood count was down to 0.5, even though I was on a shot to bring it back up. (A $10,000 shot!!)  I am now just doing the Herceptin every three weeks. My oncologist said that there have been no studies on Herceptin only, without the TX, so they don't know how well it will work. Only time will tell, I guess. I, too, am on Warfarin, hopefully just a few more months, though. Between the stoma and the Warfarin, my diet is extremely limited... At least, knock on wood!, I have had no bad side effects from the Herceptin. I am truly greatful for this. If you look around any corner, you can always find someone worse than you are, so I try to be as upbeat as possible. Just thought there may be someone on the board that had taken only the Herceptin. thanks again, and best wishes to you.

  • Alicethecat
    Alicethecat Member Posts: 535
    edited November 2012

    Hi I Will Make It Thru

    There are ladies on the HER2+ Support Group who are only on Herceptin.

    http://her2support.org/vbulletin/

    Best wishes

    Alice

  • Alicethecat
    Alicethecat Member Posts: 535
    edited November 2012

    Hi I Will Make It Thru

    My neutrophils dropped to 0.37 after my first infusion of FEC but I had the Neulasta injection and then switched to Neupogen and the chemo continued!

    Still here and recovered well after chemo.

    However, I appreciate that everyone is different and you/your oncologist have your own view of the risk you are prepared to take.

    I didn't realise that I could have been attacked by a virus when I went down to 0.3. Just thought of bacteria!

    Best wishes

    Alice

  • SeattleMama
    SeattleMama Member Posts: 147
    edited November 2012

    Here's my treatment - I think its through Dec 18, 2012

  • MizMarie
    MizMarie Member Posts: 332
    edited November 2012

    About a week after my first round of chemo in August 2011, I developed fever a chills, which I had been warned about, but I didn't call the MO until I felt so sick I could barely walk.  When I went in, my white count had dropped to .9, and my neutrophils were at .06.  I spent a couple of days in hospital, but I recovered quickly.  From then on, I was given a Neulasta shot to protect my immune system, and had no further problems.  I do remember at my consult appt being told to call in if my temp went above 100.5, but it was not emphasized why this is so important.  Lesson learned!

  • SeattleMama
    SeattleMama Member Posts: 147
    edited November 2012

    Thanks Marie, good to know, Neulasta!  So glad you went in. That would have scared me.

  • marjie
    marjie Member Posts: 1,134
    edited November 2012

    Ah yes!!  The fevers....Neulasta didn't work for me so I ended up having to learn to inject myself with Nuepogen daily for 10 days after each chemo.  Unfortunately, on day 7, every single time - fever & hospitalization - I actually had a bag packed because it was like clockwork.  My WBC would actually zero out and I finally ended up having to have a blood transfusion.  I was too wiped out to really care, but it was stressful on my family.

    All that being said - it DOES pass. Herceptin was a walk in the park compared to the FEC-D.  Just more tiring than anything.

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