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Old 12-17-2007, 07:07 PM   #1
Lani
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Good news for the holidays--how herceptin has changed the prognosis of her2+ breast

cancer

http://www.abstracts2view.com/sabcs/...u=SABCS07L_435
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Old 12-17-2007, 08:32 PM   #2
Margerie
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I wonder if the her2+ population in this study was also hormone+. Doesn't specify??
I am triple + and always wondered if the hormone+ trumps the her2+ or vice versa.
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Dx 10/05 IDC, multi-focal, triple +, 5 nodes+
MRM, 4 DD A/C, 12 weekly taxol + herceptin
rads concurrent with taxol/herceptin
finished herceptin 01/08
ooph, Arimidex, bilateral DIEP reconstruction
NED
Univ. of WA, Seattle vaccine trial '07
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Old 12-17-2007, 09:50 PM   #3
Bev
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M. I think the luminal includes some hormonal positivity, one or the other. So I think this is good for you. BB
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Old 12-18-2007, 08:41 PM   #4
Becky
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It is always better to have the hormone receptors be positive - even if only one is and two are better.
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Kind regards

Becky

Found lump via BSE
Diagnosed 8/04 at age 45
1.9cm tumor, ER+PR-, Her2 3+(rt side)
2 micromets to sentinel node
Stage 2A
left 3mm DCIS - low grade ER+PR+Her2 neg
lumpectomies 9/7/04
4DD AC followed by 4 DD taxol
Used Leukine instead of Neulasta
35 rads on right side only
4/05 started Tamoxifen
Started Herceptin 4 months after last Taxol due to
trial results and 2005 ASCO meeting & recommendations
Oophorectomy 8/05
Started Arimidex 9/05
Finished Herceptin (16 months) 9/06
Arimidex Only
Prolia every 6 months for osteopenia

NED 18 years!

Said Christopher Robin to Pooh: "You must remember this: You're braver than you believe and stronger than you seem and smarter than you think"
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Old 12-18-2007, 09:25 PM   #5
Margerie
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I know that generally hormone + patients have a more favorable prognosis than hormone negative, her2 + tumors are considered more aggressive than her2- and the majority of HER2+ patients are hormone negative. So if you are strongly er+ and pr+ and her2 3+, is this double good (two targets for treatment) or is this bad because of the er/her2 crosstalk?

I haven't seen any studies differentiating the her2+ population- except the er+/pr- tamoxifen study.

Yes, this is why we need a tumor registry to figure out all this stuff!
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Are we there yet?


Dx 10/05 IDC, multi-focal, triple +, 5 nodes+
MRM, 4 DD A/C, 12 weekly taxol + herceptin
rads concurrent with taxol/herceptin
finished herceptin 01/08
ooph, Arimidex, bilateral DIEP reconstruction
NED
Univ. of WA, Seattle vaccine trial '07
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Old 12-18-2007, 11:28 PM   #6
Karen W
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I think I remember reading that because of the crosstalk with the er/pr and her2 receptors, Tamoxifen is not an effective treatment for Her2+ bc. That is why (supposedly) Aromatase Inhibitors are better when you are Her2+ and er/pr+.

I think this is correct but not certain.

Karen
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