How many Stage III gals never go to Stage IV?

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IllinoisNancy
IllinoisNancy Member Posts: 722
edited June 2014 in Stage III Breast Cancer

Hi,

I know we have a post about moving from stage 3 to 4 but I'm more interested in hearing from the ones who never change from Stage 3 and live a nice long life.  I hope to get lots of positive answers.

Thanks,

Nancy

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Comments

  • jpsgirl96
    jpsgirl96 Member Posts: 240
    edited June 2011

    Hi Nancy, We have a thread here on the Stage III forum for 5+ years out; if you haven't seen it, have a look!! Lots of good stories there.

    There are so many different stories, different situations, different ages...and cancer itself is not really one disease but many.  I am sure you have also heard it said that there are no helpful percentages: there are only two numbers 0% (I don't have it) and 100% (I do have it).

    Can I ask a pesky question?  From your signature stats, I am surprised you are Stage IIIb.  I am not doubting, just wondering what makes it so for you.

    All the best, Leigh

  • IllinoisNancy
    IllinoisNancy Member Posts: 722
    edited June 2011

    Hi,

    I am Stage IIIb because my local recurrence in my left breast had showed up on the skin.  It looked like 2 small pin size musquito bites.  My BS said they don't like to stage local recurrences but since it was on the skin, I'm a stage III.  I looked up the stages on BC.ORG and it said if it went to the skin it was a 3b.  Other than that, my tumors have been very small and I had a clean PET scan.  Another odd thing was my Oncotypedx was a 9 in 2006 and the doctors said my recurrence was exactly the same kind of cancer, ILC, Pleomorphic, ER++, PR-, Her-.

  • diana50
    diana50 Member Posts: 2,134
    edited June 2011

    well so far so good here. 9 years .  my friend is 11 years; very large tunor and 10 + pos nodes.  there are many of us out there who are doing well.,

  • mrsnjband
    mrsnjband Member Posts: 1,409
    edited June 2011

    I am IIIb because I had inflammatory breast cancer.  It has been 3.5 years with no reoccurance. The odds for reoccurance is in the first 2-3 years & for the first 5.  So far so good! NJ

  • everyminute
    everyminute Member Posts: 1,805
    edited June 2011

    Let's see - I personally know

    Stage 3 10 years

    Stage 3 7 years

    Stage 3 33 years!

    Stage 3 25 years!

    and that is just off the top of my head

  • Claire_in_Seattle
    Claire_in_Seattle Member Posts: 4,570
    edited June 2011

    If you look at the American Cancer Society 5 year statistics, they are very discouraging.  They are also very out of date as reflect patients treated ten years ago.

    I am not going to share these, but rather want to share the 10 year survival statistics from MD Anderson.  These are for regional disease, and include Stage IIb and Stage III.

    • For women diagnosed, between 1985 and 1994, 10 year survival was 57.4%
    • For those diagnosed between 1995-2004, it was 74.1%

    I would think we should expect similar improvements for the group diagnosed 2005 or later.

    The article can be found at:

    http://www.mdanderson.org/newsroom/news-releases/2010/md-anderson-study-finds-increases-in-five-10-year-survival-at-every-stage-of-breast-cancer-over-six-decades.html

    I found this point very interesting considering all the discussion about the value of conventional therapies.

    "A number of MD Anderson's research milestones have impacted clinical care and breast cancer survival, both at the institution, and beyond, says Buzdar, including: combined modality approach to the treatment of the disease; utilization of systemic therapies prior to surgery; refinement of
    chemotherapies, specifically the incorporation of anthracyclines, taxanes and biologics, and newer hormonal agents like aromatase inhibitors."

    The table showing improvement over the years is so very encouraging.

    One other point is that "Overall" is only that of MD Anderson, so cannot be compared to cancer patients throughout the US.  But you can look at local, regional, and distant disease and see what is possible with excellent treatment.

    Such amazing news about overall progress. - Claire

  • Pure
    Pure Member Posts: 1,796
    edited June 2011

    Thats a great article Claire..Next time I have a crying wining fearful fit can you remind me of that article::) lol

  • IllinoisNancy
    IllinoisNancy Member Posts: 722
    edited June 2011

    Hey Everyminute....I Love your stats!!!!

    Thanks for sharingSmile

  • KerryMac
    KerryMac Member Posts: 3,529
    edited June 2011

    Wow, Claire, that article is great. What a huge jump for us. Great to see, and I would imagine that trend continues, to give us even better stats now. Thanks for posting.

  • AnacortesGirl
    AnacortesGirl Member Posts: 1,758
    edited June 2011

    Thanks Claire!  I was hoping to find the full text of the study but no luck.

  • Claire_in_Seattle
    Claire_in_Seattle Member Posts: 4,570
    edited June 2011

    Some things I can think of that are standard protocol now vs 10 years ago:

    • 3rd Generation chemo protocols.  Interesting for me that being in the SWOG 0221 raises my chances of survvival by about 4% vs 2nd Generation Protocol for AC +T.
    • Aromatase Inhibitors vs Tamoxifen only.  Some incremental benefit here too.
    • Herceptin for anyone who is an appropriate candidate.
    • Better equipment for radiotherapy.
    • We are able to manage side effects and toxicities much better so a greater percentage of patients complete the therapy.  Major important.

    I think too that we are starting to understand the importance of things we can do post active treatment, the most important of which is exercise.

    And we can go on to live normal, productive and happy lives afterwards!!!!

  • Claire_in_Seattle
    Claire_in_Seattle Member Posts: 4,570
    edited June 2011

    Anacortes Girl.....think just a press release summarizing statistics from MD Anderson.

    I posted because I think reflect where breast cancer treatment is going, as opposed to the national stats that include everything, including those who forego any treatment.  These are also more current.   Importantly, they show the effect of advances in treatment on survival.

    I think CancerMath uses something similar in their algorithms.  Because stats are so much more favorable than what the American Cancer Society provides.  I also find CancerMath statistics consistent with trials for the chemo protocol I received.

    I will be very curious to see what Adjuvant Online gives if and when they release 9.0.

    One of my big learnings when I first reviewed the earlier studies that SWOG 0221 is a follow-on to, was how much better the survival statistics were vs the ACS ones.  Then the light dawned.  These women completed the therapy!!!

    Even women in the control groups (2nd Generation AC + T) were much better than the population as a whole.  Very important learning.

  • ck55
    ck55 Member Posts: 346
    edited June 2011

    Claire, just out of curiosity, where did you go for your treatment.

    I was at Swedish with Dr Buchanan as my BS and Dr Kristine Rinn as my onc.Felt I got great care there.

    Cyndi

  • Claire_in_Seattle
    Claire_in_Seattle Member Posts: 4,570
    edited June 2011

    I was treated at Group Health which does share some resources with Swedish.  I thought Dr Tien-Bao Chao did a superb job with my surgery, and my oncologist was certainly up on the latest research (I have someone else now). 

    One of my learnings from this experience is how happy I was not to have to "doctor shop".  Someone from Canada mentioned this, and I was happy to be referred to the best person for my particular issue.  (Similar to a Level 1, Level 2, Level 3 support model in technology.)  I could say no, or ask for a second opinion, but I was very happy with the care I got.

    And so happy not to have to doctor shop.  I knew I had the right person when the people booking my appointments would say "O good, you have......"

    It is also great being within a system with online medical records.  Your history is updated, so the next person in line just updates.  So efficient, and it's all there.

    This was really helpful when I finally circled back to my Internist (who I had never met, as needed all the exams done prior to treatment, and this was a new health system for me) and say: "you can see I have had quite the year".

    And then, he could check to make sure all the rest of me was OK.  It was.

  • sweetbean
    sweetbean Member Posts: 1,931
    edited June 2011

    Claire,

     What is the SWOG 0221?  I just did AC+T and am doing Herceptin.  Did I have 2nd generation chemo?  Or 3rd generation?  I'm a little confused -thanks! 

  • Rennasus
    Rennasus Member Posts: 1,267
    edited June 2011

    Just wanted to share that my sister had Stage III breast cancer in 1984.

    She had a BMX and chemo and just celebrated her 27th cancerversary!

  • elmcity69
    elmcity69 Member Posts: 998
    edited June 2011

    this is awesome - thank you, Rennasus, and happy for your sister. hope you are doing well. i just had my TE removed last week - no muss, no fuss. i'm back to practically pre-surgery activity (except a yoga banx4 weeks, boo hiss!).

    claire, you made my day. love love love it. going to email it to my hubby, who gets fearful and sad but tries to hide it. he's a nurse practitioner and i think his medical expertise is "too much information", if you know what i mean.

    anyway, hugs to all.

  • Claire_in_Seattle
    Claire_in_Seattle Member Posts: 4,570
    edited June 2011

    Hi Sweetbean.... The major difference between 2nd and 3rd generation AC + T protocols is whether dose dense or not.  So whether you did every 2 weeks vs every 3 weeks (2nd Gen).  Prior to Neulasta/Neupogen support they couldn't give you AC every 2 weeks because your immune system would tank too far.

    With Herceptin, there may have been other factors in the decision.  I don't know.

    SWOG 0221 was designed to test whether Dose Dense (the control, and what I got) or Metronomic (weekly, lower dosing) was superior.  The other part was weekly Taxol vs every other week.  That was the initial study. 

    That was closed back in December, and now Dose Dense AC is being tested with weekly vs every other week Taxol.

    I think some preliminary findings will be available about this time next year.

    The way the initial study was set up, I got six DD AC vs four which is the standard for 3rd Generation protocols.  I can say that I was OK, but would have found it very hard to do seven.  I don't think we will know for a number of years if any survival benefit.  There was more toxicity though.

    The continuation now is doing the standard 3rd Generation for AC (four DD).

    You can find more information if you do a search on SWOG 0221 on the Southwest Oncology Group site.

  • sweetbean
    sweetbean Member Posts: 1,931
    edited June 2011

    Oh, thanks!  I did dose dense AC and Taxol, although I should have done dose dense AC followed by 12 weekly Taxol and Herceptin.  Onc screwed up and we didn't know about the Her2 status until well after chemo.  I started it 8 weeks PFC.  Thanks for the info!

  • Claire_in_Seattle
    Claire_in_Seattle Member Posts: 4,570
    edited July 2011

    sweetbean....suspecting the DD AC + T has already knocked those suckers to kingdom come.  Important with Herceptin is to do for one year, which I am sure is the case.

    Am sure you will be just fine. - Claire

  • Octobergirl
    Octobergirl Member Posts: 334
    edited July 2011

    Sherri,  I had TAC at 3 wk. intervals in 2009. I asked my oncologist about dose dense tx. and he said data supported TAC as the most efficacious treatment for my situation.

    Claire and Nancy, thanks for starting this thread and posting the MDA report. Lately, I've worried a lot about recurrance because of bone issues. This is reassuring!

  • Joviangeldeb
    Joviangeldeb Member Posts: 213
    edited July 2011

    Just chiming in to say that I've been ned for 3 years now.

  • christine47
    christine47 Member Posts: 1,454
    edited July 2011

    Sherri,

    RE, TAC for stage 3, my friend just completed 6 rounds of TAC every 3 weeks for her stage IIIb, grade 3 BC.  I finished mine 2 months ago.

  • NancyD
    NancyD Member Posts: 3,562
    edited July 2011

    I'm another TAC x 6 lady. I finished my first four doses just about three years ago and was preparing for surgery. I had two more doses after surgery. They were all three weeks apart except for the surgical break.



    After thinking about it I'm very glad I had it that way as I was able to continue working without much problem. I only had to take a couple of days off every three weeks. I have people working for me now...healthy people...who do that as a normal thing, lol.



  • diana50
    diana50 Member Posts: 2,134
    edited July 2011

    TAC here; clinical trial in 2002. still NED

  • sugarplum
    sugarplum Member Posts: 318
    edited July 2011

    And me too - TAC X 6, 3 weeks apart in 2006 (oh, how I loved that third week!). Still NED & forever hopeful...

    Julie

  • gardenbird
    gardenbird Member Posts: 31
    edited July 2011

    I'm also a TAC x 6 at 3 week intervals in 2007.   Had my treatment here in the Netherlands.   I'm doing really well (still underlying fear, but nearly normal), and like Julie, hoping for the best 

  • kmur
    kmur Member Posts: 912
    edited July 2011

    Hi Nancy and Ladies,

    I am stage 3 also. I hope you don't mind me saying what a wonderful thread this is.  I love to read or hear positive stories. Thought I would share mine... I really think us stage 3 girls are going to change all those old stats we read.  I just keep hearing so many positive stories now that I too have BC.  I rarely speak about my BC to people,but needed to buy my first bra after recon surgery.  The lady that helped fit me was so nice. Somehow I told her about my BC and so on. Turns out she had stage 3 breast cancer 17 years ago and back then treatments were not quite as good. She said her cancer was kind of scary,but here she is doing fine.  I think I was supposed to meet her that day I guess. All those stories make me very hopeful. Thanks for sharing and blessings to all of you

    Kim

  • jpsgirl96
    jpsgirl96 Member Posts: 240
    edited July 2011

    TACX6 every three weeks here too, March-July 2006.  I wanted to commute from Florida to Washington DC to work, and that meant the every three week protocol worked better for me, and the results my onc was seeing for dense-dose AC+T and TAC were similarly encouraging.

    What I had been seeing from Adjuvant Online when I was still looking was that the advent of these "third" or maybe "fourth" generation chemo regimens PLUS the anti-hormonals for those of us who are ER/PR positive has made huge percentage improvements even for larger tumors and node-positive breast cancers.

     Alas, for an ILC-er like me, there is still not enough data to understand what really works better to prevent recurrence, and even some doubts as to whether chemo does much of anything...BUT the recurrence rates are definitely NOT higher for us ILC folks, and may even be a bit lower, even if the chemo isn't the best trick in the box.

    I never know whether to recommend it, but there is a wonderful book - a total page turner for those of us who have had cancer - called "The Emperor of All Maladies".  It gives great insight into the complexity of cancer as a disease, and into the progress (and lack thereof) in treatment.  I loved it, and it helped me see how little use "statistics" are for non-clinicians (i.e. patients).

  • kmur
    kmur Member Posts: 912
    edited July 2011

    Hi jpsgirl96,

     Thank you for your post. I so agree with your thoughts and I am going to look into that book.

    Thanks,

    Kim

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