Statistics and herceptin

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  • GramE
    GramE Member Posts: 5,056
    edited October 2008

    Laura, I lived in our house 36 years and remember when it came time to update.  We did windows, carpets, kitchen, but never got to the bathroom (for remodeling ... )  When I sold the house the new people LOVED the old  60's blue and white ceramic tile in the bathroom and the tiny octagon tiles on the floor.   The other bathroom was a pale peach and off white mix of ceramic tiles.  This apartment has stark white everything and i do miss the color.  White cupboards and counter top in kitchen and vanities in bathrooms, white tile in bath and shower, even white floor tile.  Like being in a hospital, sort of...  Good luck on the door project.

    I see that fall is in the air - much cooler temps, but I am not complaining - yet.   Have a good weekend,  Hugs,  Nancy 

  • tbird57
    tbird57 Member Posts: 150
    edited October 2008

    I watched the movie tonight and thought it was great.  I've also read Robert Bazell's book, HER2, which the movie was based on.  But I had a question: in the movie, there was a line that stated something like this  "a third of the women who have breast cancer have a very aggressive form of it and they will die from it."  Is this true?  I know HER2+ women have an increased risk of recurrence and a reduced overall survival rate, but I didn't think all HER2+ women were absolutely doomed without herceptin.  Was this just dramatic license?  Also in the movie, they said that not all women respond to herceptin.  Is there a way to tell who is, who isn't?

  • henny
    henny Member Posts: 89
    edited October 2008

    The way I understood it from when I was first diagnosed was that if you had Her2 and did nothing you would die, if you did surgery only, you had a 50% chance of no recurrence. With chemo is goes to 70% and with Herceptin it goes to 85% My numbers may be a little off but that's the gist. I didn't get a good answer for how these numbers relate to stage.

    I did think it was powerful when at the end of the movie the stadium was filled with all of us. 

  • Estepp
    Estepp Member Posts: 6,416
    edited October 2008

    The way Henny described it is the way I was told at DX too. There was a commercial   in the middle of the movie that talked about a test that our doctors can give us to see if Herceptin is responsive. I am going to ask my Oco about it tomorrow.

    I do believe that woman who had her2 BC before Herceptin, were a a huge risk of death. Because it is so fast growing and not always as responsive to chemo. BUt remember, they did not even test for the her2 gene  until like.. somewhere in the 90's. Remember in the movie/book the woman who, at the end, was given 4 months to live when the cancer came back.. and she was asking if there was ANYTHING she could try.. and her Onco told her that "if" she tested positive for her2 she could get in a third phase trial.. and she said... how do I know if I am Her2.. and  he said "we'll test you". Well, this was 4 years AFTER her original dx of BC., about 1996ish...

    We are living in a blessed time to have this type of cancer.

    Gods Love,

    Laura

  • Anonymous
    Anonymous Member Posts: 1,376
    edited October 2008

    Laura,

    I agree with you.  We are blessed to have so many options (herceptin, tykerb, SUPER herceptin) as her2+ patients.  I took notice of that commercial too.  Interesting.

    When I was originally dx'd in 2002, I met a woman in my first support group whose cancer came back quickly and she was her2+.  I remember her saying she wished she had gotten into trial at that time to receive herceptin adjuvantly.  She always said if she had gotten herceptin with original tx, she might not have gotten recurrence so soon.  Unfortunately, she did not survive her mets.  I miss Cheryl and think of her often.

    What I want to know is why do some of us respond so well to herceptin and others don't.  Perhaps their bc has mutated.  I think I have a big case of survivor guilt. 

    Knowing how blessed I am,

    Bethie

  • bluedasher
    bluedasher Member Posts: 1,203
    edited October 2008

    TNT, I wondered about that same line when I heard it. I think it must be an oversimplification. Everything I've read and what my oncologist told me is that for my <1 cm, stage I, 100% HER2+ cancer, with lumpectomy, radiation and no chemo,  I have a less than 20% chance of recurrance and an about 10% chance of dying.

    Perhaps what was really true is that if HER2+ cancer got past a certain point like stage IV, it would be fatal without Herceptin. Maybe they simplified it. I also thought that HER2+ was around 25% of cancers rather than 1/3. Or possibly the statement was what they though at the time that Herceptin was being developed. Since HER2+ testing was pretty new at the time, they wouldn't have had as much statistics developed on i  

    I  also noticed that they said several times that Herceptin doesn't have any side effects which isn't quite true. But since it has much less side effects than chemo and they were just starting to test it, that may have been what they thought then. 

    It was a very interesting movie and I'm glad I saw it.  If there were minor inaccuracies or simplifications, it still is great to have a movie out there letting people know that research does sometimes produce breakthroughs. I'm grateful to Dr. Slamon for persevering and to Revlon for helping to fund his research.

  • Liz08
    Liz08 Member Posts: 470
    edited October 2008

    Ladies-

    the couple that was in the commercial for the test to check if Herceptin is working are Christine & Joe who are the creators of a forum for those who are her2+++, their website is www.her2support.org.  It's a great website/forum for those who are her2+++ 

  • GramE
    GramE Member Posts: 5,056
    edited October 2008

    Liz, that link does not give me anything except 2 links to videos.   Maybe it is my Macintosh - and/or fire wall settings.   

  • SecretCancer
    SecretCancer Member Posts: 34
    edited October 2008

    Hi everyone --

    Correct me if I'm wrong, but I didn't think there was any way to test that Herceptin was "working" unless you had metastatic breast cancer and can see (in CT scans) if the cancer is spreading or shrinking.  For those of us without mets there is no way to tell.

    Kim

  • Liz08
    Liz08 Member Posts: 470
    edited October 2008

    Lefty-

    you have to chose an area of the forum you want to go into such as click on "message boards" and you get to see the topics in the forum and you chose which one you want. 

    I clicked on "message boards" here's the link.  http://her2support.org/vbulletin/, if you're still having trouble let me know.  The members on the her2 forum are very knowldegable about the various stages of bc that is her2+++.

  • Pugmama
    Pugmama Member Posts: 4
    edited October 2008

    I was dx in 6/06 with IDC w/lobular features, 3 tumors, grade 3, lymph and vascular invasion, ER/PR+ and Her2+...I am still here...celebrating my 2 yr mark from surgery date, 8/9. At my visit last week with my Onco he told me that 70% of pts dx's with the aggressive form I had have already recurred...I have not...though the statistics are very hard to read and hear, ignore them..it will drive you crazy..wake up thanking God for another day and live your lives...

  • GramE
    GramE Member Posts: 5,056
    edited October 2008

    Liz, thanks for the link - it worked great.   

     Pug:  congrats - dancing with NED  ( no eveidence of disease ) is super.   

    I had my penultimate ( next to last ) Taxol and Herceptin  today.   Konked out for 4 hours and doing prob will be up till all hours due to the steroids.    Herceptin for almost another year every 3 weeks is next, with surgery consult on Nov 6.   

  • BethNY
    BethNY Member Posts: 2,710
    edited October 2008

    I was given similiar stats- w. just surgery 50% with chemo too 70% Herceptin 82% and had I chosen to add Tamoxifen it would have been 87%....

    I do want to tell everyone that's on their yr of Herceptin, that your hair grows SOOOOO much faster when you're finished! Something to look fwd to.

  • GramE
    GramE Member Posts: 5,056
    edited October 2008

    I had # 11 of 12 weekly Taxol and Herceptin and fuzz on my head is very much there.  Some had said to keep massaging your head to make it grow faster.   

    Question:   I have surgery consult on Nov 6.   After # 12 of taxol and herceptin I am to have only Herceptin every 3 weeks.  Do or did you schedule it, even if surgery is going happen or wait till AFTER surgery to do it.  Does one coordinate it with surgeon or onco since it is not "chemo" ???

    Have a great weekend. Enjoy, smile, laugh - Hugs and Blessings,  Nancy 

  • Estepp
    Estepp Member Posts: 6,416
    edited October 2008

    you know, it is weird.. I have 5 more chemo's to go ( taxol/herceptin) and I have always had fuzz on my head. I have lost about 75% of the hair on my head... and 55% of the hair on the body. I just find it strange that some of us keep hair... some do not...

    Laura

  • GramE
    GramE Member Posts: 5,056
    edited October 2008

    Laura, I had 4 Dose Dense A/C before the the combination and hair was GONE in 15 days.   

    A funny:  Chemo friend Nadine finished chemo 2 weeks ago and she has no hair on head, but at her surgical consult today, she had to raise her ams for exam and discovered she has underarm hair but nothing on her head.    

  • DianaT
    DianaT Member Posts: 532
    edited October 2008

    Hair is such a funny thing (and I am not laughing). I had about 75% of my body hair until the taxotere (4 rounds), halfway thru my eyebrows and eyelashes started to thin out and my the last treatment I had one (1) eyebrow hair and I kept that bad boy on ~ everyone told me to pluck it.  My hair is growing back, finally full enough that I am feeling more and more comfy ~ one guy said I had a cute cut (I ignored him, Erick said thanks).  I have been told that once herceptin stops hair grows much much faster too!  I am looking forward to that too.  My eyebrows are still pretty much nonexistant and my lashes are there but still short.  I finished chemo May 22, 08

  • BMac
    BMac Member Posts: 650
    edited October 2008

    BethNY you are so right about slow hair growth on Herceptin.  I finished chemo on March 13th and I'm appalled at how slowly my hair is growing.  I'm on Herceptin until early January and I can't wait.  I had ovarian cancer 6 years ago, finishing chemo Mar 6th/03 and I know that at this point I had way more hair.  That's been my biggest complaint.

  • DianaT
    DianaT Member Posts: 532
    edited October 2008

    also, my dr. gave me statistics that were much more doom and gloom than what you all have been told.  I guess because of my staging, I don't know.

  • GramE
    GramE Member Posts: 5,056
    edited October 2008

    I also have one eyebrow hair on the left, 2 on the right and refuse to pluck.   2 eyelashes on each side. If I used mascara, it would last a year or more !!

    Since I will be on Herceptin every 3 weeks until next June or July, I expect that hair is not going to be my "crowning glory".  There is more and more white fuzz - and only one more taxol and herceptin to go.  Just think of all the money saved on hair products and hair cuts and the time to groom it.   In the shower, out, no shaving pits or legs, no wirey chin hairs,  toss on a wig or head cover, ready to go after taking more time deciding what to wear.    

    If you are near Sally Beauty Supply, they have eyebrow stencils for $ 2.99.  I got them but have not tried yet.  Sephora has them for much more and a whole kit with pencils, gel, etc.   Both are online, but shipping is pretty high in my opinion.   I rad that if you put loose powder first, pencil sticks better -again I have not tried it yet.   And mascara also sticks better than pencil.  

    In a way this is like playing dress up as a kid -- play around and hope you dont end up looking like the painted lady !!!    HUGS, Have a great weekend,   Nancy 

  • Brenda_R
    Brenda_R Member Posts: 509
    edited October 2008

    A funny thing about eyebrows-

    I read that after you lose your eyebrows to chemo and they grow back in, when they "shed" again, they shed in clumps.

    I recently found out that's true. Lol  I have had missing chunks out of both eyebrows for the last few weeks.  I am over 1 year out of chemo, so I guess it takes awhile for those to shed. 

  • tbird57
    tbird57 Member Posts: 150
    edited October 2008

    Oh dear, that's not good news about the slow hair growth with Herceptin.  Does this mean I'll be close to hairless until the end of 09?  Good grief. 

    bluedasher, I read the book by Robert Bazell and that line isn't in it anywhere, so I figured it's just dramatic license.  The stats my doc gave me are about the same as everyone else is quoting with a similar stage and diagnosis.

    Love to all,

    Teena 

  • vhqh
    vhqh Member Posts: 535
    edited October 2008

    I am on Herceptin for life if it keeps working for me, finished chemo in February of this year and quit wearing a hat in May.  By July I had a head full of thick cute curls that I loved so yes, it can grow back good while still on Herceptin.  Unfortunately for me the hairs gone again but oh well, it was nice while it lasted!   :)

  • tbird57
    tbird57 Member Posts: 150
    edited October 2008

    I'd love to have a head full of curls...I'll keep that positive thought!

  • GramE
    GramE Member Posts: 5,056
    edited October 2008

    I had a head full of thick naturally curly hair - looked like Little Orphan Annie when wet.   It would be nice to have it back again since it is cold now without hair.  There is some white fuzz around the fringes, and my last Taxol and Herceptin is tomorrow.   Positive thoughts are going out for all,

    Hugs,  Nancy 

  • HappyTrisha
    HappyTrisha Member Posts: 614
    edited October 2008

    Just did a quick scan of the posts but wanted to add my two cents to this topic.  I would crawl on my hands and knees if I had to in order to get herceptin.  I was one of the very lucky kids who received it as part of the early-bc herceptin trials going on at Dana Farber.  I had it with navelbine, then my mastectomy, then had A/C, then rads, then finished up the year of herceptin.  I also had a second mastectomy in the process (that one voluntary).    Then I had reconstruction.  This December will be 5 years since I was diagnosed.  I am currently on arimidex as I was triple positive.   I had no side effects to speak of when I was on the final stretch of herceptin.  There is nothing I would change in the entire process.  I did everything I could to increase my chances at survival.  My bc was aggressive, and so we went with aggressive treatment.

    As far as I am concerned, I am cured.  I had angels on my shoulders throughout this process and it was definitely an angel who led me to Dana Farber and the trials where I was guaranteed herceptin as part of the trial.

    Thank you angels, and GO HERCEPTIN!

    Trisha

    Smile 

  • Estepp
    Estepp Member Posts: 6,416
    edited October 2008

    AWESOME TRISHA!

    That is so awesome! Thanks for sharing your story!

  • tbird57
    tbird57 Member Posts: 150
    edited October 2008

    Laura, that's a new avatar for you, isn't it?  Looking good, girl!

  • my2boys
    my2boys Member Posts: 339
    edited October 2008

    Thank you for posting your story HappyTrisha.  It brought tears to my eyes.  You are a brave woman.

    God Bless

  • Estepp
    Estepp Member Posts: 6,416
    edited October 2008

    LOL... yes, it is a new avatar... it is me in the wig I wear all the time now. Looks good for winter. I have about 25% hair...LOL.. on my head... so when I go out, that is my wig... I thought I should post how I look now.. :)

    I WISH it was my hair.. but nope... I have 4 more chemos ( taxol) and then herceptin till next yr.. so that wig may be with me awhile...:)

    I have never looked good in the wraps... so I wear a beenie around the house ( it is cold here) and my wig when I leave the house...:)

    Laura

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