Complete Pathological Response!
Hello friends, I have a bit of good news to share that I hope will be encouraging for others that are just faced with this very scary diagnosis. After 7 months of chemo I just had my scans and the pathology from my bmx and the results are in - I've had a complete pathological response, no cancer cells found at all!
I thought I'd both share that good news and give details about my treatment, for the interested or for posterity:
- I had 5 rounds of A/C administered every three weeks
- After that, I had weekly Herceptin from January to late April, along with Taxol. The Taxol was administered weekly for three weeks, with a "rest" week in between (although my last cycle was messed up because they accidentally gave me Taxol for 7 weeks straight with no break. The only consequence of that was increased fatigue
Comments
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Congratulations! That's a great feeling!
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Glad to hear it. I'm glad all the treatment has worked well for you. Relax for awhile and enjoy this time. Hope you stay NED for a very long time.
Terri
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Awesome! Congrats!
Lori
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Thank you!
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NED? You're gettin' it on with NED? I'm so jealous! I've never met him, personally. GOOD GOING though! :-)
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Wonderful news and praise God!
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Thank you so much! Yes Lena, I certainly never thought I'd meet him, lol!
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Congratulations, sweet Pam!! I am so happy for you!
God bless,
Marianne
P.S. Does this mean you change your name to Ned? Teehee!
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Pam, so good to hear from you! Especially with such good news! Congrats! How did your surgery go? I hope you had a quick recovery!
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So happy for you. I am getting close on finishing chemo and just met with a surgeon myself.
We all want to be you!!
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Marianne if it would keep me NED forever I'd change my name in a heartbeat, lol!!! I'd even embroider it on all my underwear.
Thank you bkj!! It went just fine - I'm having some skin neurological problems from the mx - burning, "bee stings" and such, but they'll pass. I hope, hahah.
Thanks Lily! Best of luck to you as well. With my specific dx it's likely to come back fast (but taking herceptin improves my chances), so I am planning on loving every day whether it has it's faults or not.
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PaminWV - We have very similar dx. I am in the Neratinib trial right now. Are you? It's for HER2+ patients.
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Hi Leisa,
Right now I have to do my 6 1/2 weeks of rads and simultaneous Herceptin...I'm not sure what wil be after that!
My Onc (and Lori!) told me this was the best possible response, and the best predictor of prognosis - in a good way. I am very lucky so far.
I know there are answers and commonalities that could predict cancer and IBC in particular, but we just don't know about them yet. And I think my response is in large part being Her2+++ (I didn't realize it til recently but I am off the freaking chart with Her2) chemo worked well and I could take Herceptin.
But if you're at all interested, as you saw my treatment seems to be like everyone else's, but I received my A/C every 3 weeks and then Taxol 3 weeks on, 1 week off, with Herceptin administered every week when Taxol started. The other big difference was that I never received and Procrit or other blood-boosting shots, and I had a very easy time of chemo in general. My TMI statement I always say is that I never threw up, but it does tell you that I was feeling pretty good. The only reason I didn't throw up was from taking Emend, promethazine, zofran, and sometimes even ativan - *everything* seems to make me nauseated as I get older. I had a double mx with left side being prophylactically removed.
So, those are the only differences I saw in my treatment vs what I've read. I'm sure not suggesting if someone's counts fall they should refuse treatment because I had a good result or anything similar, I sincerely doubt the differences had anything to do with it but who knows? I'm just kind of recording for posterity's sake.
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Pam, I am so glad for you! Congrast!!!!
Pam, how did u find your doctor? We live close to each other, I live in Ct. I have read that a right doc is a very important part of treatment. Did you go to Memorial Sloan - Kettering Cancer center in NY? Did you wotk during chemo?
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Thanks so much, Andrea!
I just went to the University cancer center and was assigned my oncologist (the head oncologist) because IBC is rare. So in that case, IBC definitely worked for (rather than against) me. I've never been anywhere for a second opinion, but if I have a recurrence I will seek a second opinion at Fox-Chase.
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Hi Pam: I'm a bit late reading your post, but that is wonderful news, couldnt be any better than a complete pathological response. Congratulations and continue to keep well and enjoying life.
Kathy
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Thank you so much, Kathy. I hope you are in or soon will be NED also!
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Hi Pam: I'ts so good that you had such a great response to the chemo. I was NED for a while but now have skin and bone mets. Ugh! I've been on Xeloda (oral chemo, 2 weeks on, 1 week off) which cleared up the skin mets very quickly but I had to be taken off the drug for an extra week due to very bad side effects -- face rash and blotches and lips blistered, as well as hand and foot syndrome. Everything has healed now and I feel good. I'm seeing the Oncologist on Weds. He may prescribe a smaller dose of the Xeloda. It's so crazy that the meds clear up one thing but then give nasty side effects.
Keep well. Kathy
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