One of my BC friend told me (not sure where she got the info. from), the stronger your ER/PR+ is, the easier your BC will recur, I read something similar somewhere on internet as well. What did your doctor say?
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Gitane Joined: Feb 2008 Posts: 829 |
Oct 18, 2009 01:24 am
Gitane wrote:
This is really not something that anyone knows. There are so many factors that affect how well we do after treatment. I have read that women who have negative ER/PR may be more likely to recur within the first 3-4 years, and that women who are positive ER/PR may be more likely to recur at a later time. Treatments affect these statistics with ER/PR negative BC more likely to respond to chemo and ER/PR positive BC more likely to respond to endocrine therapies. However, these generalizations come from statistics that apply to large groups of women with many different types/sizes/grades/stages of BC who received many different treatments. I was told that nobody knows how an individual will do. Dx 8/18/05, Pleomorphic ILC, multifocal, multicentric, G2, 1/9 nodes positive, OncotypeDX 23, ER+ PR- Her2-
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hollyann Joined: Nov 2007 Posts: 2,391 |
Oct 18, 2009 08:58 am
hollyann wrote:
I was told with triple negative, meaning ER/PR and Her2Neu negative that there is more likely recurrence the first 3 years than after 5 years and with ER/PR positive bc your chances of recurrence go up after 5 years..........In the end it is all a crap shoot no matter what......Onceyou have bc you always run the chance of recurrence no matter what....I have met a woman here in my town who is a 19 year survivor......She was diagnosed at age 21 and we all know the younger you are the more aggressive it is....I have also met women who were diagnosed later in life who are no longer here who lved only a couple of years......So we really don't know how we will all react to bc....... Hugs and love, Lucy also dx with DCIS grade 2 er/pr + her2 neg
Diagnosis: 1/15/2007, IDC, 1cm, Stage Ib, Grade 1, 0/6 nodes, ER+/PR+, HER2- |
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KerryMac Joined: Jan 2009 Posts: 1,699 |
Oct 18, 2009 10:01 am, edited Oct 18, 2009 10:02 AM
by KerryMac
KerryMac wrote:
I think the wide-spread use of AI's is too new for any reliable stats to be issued anyhow. Half the time I just think the Oncs make it up! They really just don't know. The different approaches of hormonals is so wide-spread - some use Tamox alone, some Tamox with Lupron, some suggest an ooph and an AI - hard to know what will or will not work for you. It is kind of a one shot deal - we don't know how things are going to work for us - just because they work for another woman who "on paper" looks exactly the same as you, doesn't mean that you will have a similar response. At the end of the day, you just have to do as much as you can, and then make peace with it. And go on and live your life with out any "if only's...." Kerry - Mx, Chemo, Rads, Ooph, Arimidex, Zometa
Diagnosis: 11/2008, IDC, 6cm+, Stage IIIa, Grade 3, 6/11 nodes, ER+/PR+, HER2- |
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SherriG Joined: Jan 2005 Posts: 4,861 |
Oct 21, 2009 04:00 pm
SherriG wrote:
Studies I have read do say that with er/pr+ bc, the recurrence rate increases after the first five years. I have to wonder if that is because we stop taking the anti-hormonals at the five year mark? For me, I'm going to continue on with something. Diagnosed 11/05/04 Stage 3 ILC "Lump is a four letter word!" Sherri
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yellowfarmh
Joined: Feb 2005 Posts: 853 |
Oct 21, 2009 09:34 pm
yellowfarmhouse wrote:
Hi Sherri, Are you close to 5 years too? Any thoughts on what you'll take? I've got about 9 months left on Arimidex. I went on Arimidex 6 months after dx and just after having an ooph. My onc is thinking of having me stay on Arimidex. blessings, Wendy blessings and love to all my sisters here!
Diagnosis: IDC, 3cm, Stage IIIa, Grade 3, 4/9 nodes, ER+/PR+, HER2+ |
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SherriG Joined: Jan 2005 Posts: 4,861 |
Oct 23, 2009 03:50 pm
SherriG wrote:
Hi, Wendy! It is good to see you post. I am hitting my five year mark in a couple of weeks. My five years on the anti-hormonals is in about six months from now. My onc is not sure there is any benefit from staying on anything but he is completely on board with me taking something longer for my own peace of mind. I took tamoxifen for 10 months until we were sure that chemopause was permanent. Then I moved to Arimidex. I took that for 10 months until I developed some gastro issues. I switched to Femara and have taken that for 3 years now. I am thinking about switching to Aromosin now. I have read so many reports that state that those pesky stray cells can figure out how to get around the blocking agents of the AI's. Aromosin is the only AI that works in a different manner so I'm going to try to keep those cells confused! Diagnosed 11/05/04 Stage 3 ILC "Lump is a four letter word!" Sherri
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