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wicked
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Topic: complete pathologic response Posted: Sep 17 2007 at 9:58am |
Anyone else have a complete pathologic response (cPR)??
I had chemo first and after dose dense ACT, had a cPR. I know it was in one node but because of the response, I don't know how many it really went to.
If anyone else had a cPR, can you share what your docs said about it regarding recurrence. I was pretty much shocked to hear that my recurrence/survival stats only improved by a few percentages. Not that I'm complaining because I'll take what I can get but I just thought a good response would make a big difference and it doesn't seem to.
Any thoughts?
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marathonmom
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Joined: Jul 10 2007
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Posted: Sep 18 2007 at 8:57am |
Hi,
I had chemo prior to surgery and sentinel node disection.
Following sx, there was no sign of cancer in my nodes. Since the disection was post chemo, I was concerned about the fact that we did not know the status of my nodes prior to chemo. My oncologist told me that what matters is the status post chemo: no cells is the nodes. However, from what I have been reading regarding, there is no correlation btwn node status and recurrence in triple neg. BC.
Any other thought on this?
Oana
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dx 3/6, stage2, grade3, triple neg, 6FEC, lumpectomy, 0 nodes, 4 Taxotere, rads
Oct 2007 mets to lungs and brain
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wicked
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Posted: Sep 18 2007 at 10:04am |
Oana, I believe there's less recurrence when nodes aren't involved. My doc gave me this site when I was asking about statistics:
It's usually used for chemo after surgery but the stats are the same before surgery.
I just have to be careful not to pay too much attention to statistics. I try to focus more on living and being there for my daughter. I know that every day I spend worrying is a lost day. As long as I'm feeling good, I'm going to live life to the fullest!
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marathonmom
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Posted: Sep 19 2007 at 3:21am |
You are SO right. Even though I have days when I feel down, I try to focus on the positive, on feeling good NOW and not thinking too far ahead.
I also have 2 sons and want to make the most of every day with them.
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dx 3/6, stage2, grade3, triple neg, 6FEC, lumpectomy, 0 nodes, 4 Taxotere, rads
Oct 2007 mets to lungs and brain
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Karen
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Joined: Sep 18 2007
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Posted: Sep 19 2007 at 7:57am |
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I asked my Doctor similar questions - do I have an aggressive form of tnbc, do I have a high chance of reoccurance? (my nodes are neg) She honestly said she did not know. She was aggressive with my chemo and we hope for the best. I just finished my 8 cycle of chemo and start radiation this friday. I am so tired. I met too many ladies my age and younger on their 2 occurrence. One girl is so adorable - she is 26 and the cancer is in her hip.
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Diag 4/07 2.8cm, invasive DCIS, gradeIII,-LN
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marathonmom
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Posted: Sep 19 2007 at 9:39am |
Don't give up Karen....the chemo is done and soon you will start feeling better. Rads are nothing compared to what you have already done.
Just curious, what chemo did you have?
Best,
Oana
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dx 3/6, stage2, grade3, triple neg, 6FEC, lumpectomy, 0 nodes, 4 Taxotere, rads
Oct 2007 mets to lungs and brain
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Karen
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Posted: Sep 19 2007 at 3:21pm |
Thanks for the encouragement
I had ac every 14 days for 4 treatments, then taxol every 14 days for 4 treatments. My last one was on Sept 6th - I get my port removed tomorrow and start radiation on friday (for 6 1/2 weeks) I meet with a dr every 3 months - it will be either the surgeon, the oconologist or the radiation oconologist(chemo brain can't remember how to spell) I am assuming for the first year but don't know. I am due for an mri in the next few months because my right breast looked suspicious on either my bone scan or mri can't remember.
It all happened so fast I still can't think.
Edited by Karen - Sep 19 2007 at 3:27pm
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Diag 4/07 2.8cm, invasive DCIS, gradeIII,-LN
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marathonmom
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Posted: Sep 19 2007 at 5:39pm |
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Good luck with rads and MRI results! And yes, I also have chemo brain...
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dx 3/6, stage2, grade3, triple neg, 6FEC, lumpectomy, 0 nodes, 4 Taxotere, rads
Oct 2007 mets to lungs and brain
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