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Old 10-06-2008, 03:09 PM   #1
OzzieSue
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Another interesting article from OncologyStat

HER2 Conversion May Account for Trastuzumab Resistance

Elsevier Global Medical News. 2008 Sept 4, K Wachter

HER2-positive tumors can convert to HER2-negative status in women receiving chemotherapy and the HER2-targeting drug trastuzumab (Herceptin), based on the results of a study of residual tumor tissue from 23 women.
This finding may account for resistance to trastuzumab and the incomplete pathologic response seen in some women.
"We've demonstrated that approximately a third of tumors [in patients who] did not achieve a pathologic complete response will convert from HER2-postive to HER2-negative disease," Dr. Elizabeth A. Mittendorf said during a teleconference held before the start of the American Society of Clinical Oncology's annual Breast Cancer Symposium.
HER2 is overexpressed in about 25%-30% of all breast tumors. These patients have a poor prognosis with a decreased time to relapse and decreased overall survival, noted Dr. Mittendorf of the department of surgical oncology at the University of Texas M.D. Anderson Cancer Center in Houston.
Dr. Mittendorf and her colleagues reviewed clinicopathologic data for 141 patients with HER2-overexpressing breast cancer who were treated at M.D. Anderson between 2004 and 2007. Tumors were determined to be HER2-positive either by demonstrating overexpression of the HER2 protein using immunohistochemistry or by demonstrating amplification of the HER2 gene using fluorescence in situ hybridization (FISH). The women were treated with 12 cycles of weekly paclitaxel (Taxol) with concurrent trastuzumab, followed by four cycles of fluorouracil, epirubicin (Ellence), and cyclophosphamide (Cytoxan), also given with concurrent trastuzumab.
Of 141 patients, 51% achieved pathologic complete response, which was defined as no evidence of invasive disease in the breast and axilla at surgery. At a median follow-up of 10 months, 3% of patients achieving a pathologic complete response experienced a recurrence versus 10% of those achieving less than a pathologic complete response.
Pre- and post-therapy tissue was available for 23 patients with less than a pathologic complete response.
In 16 tumors that were initially HER2-negative, repeat FISH showed that the residual tumor obtained at surgery remained HER2-negative. Seven tumors (30%) that were initially HER2-positive became HER2 negative. The researchers were able to reanalyze the pre-treatment biopsy tissue to confirm initial HER2 amplification of these tumors.
"This could represent a treatment effect in that we've selected out the HER2-negative clones. The HER2-positive clones have been treated and the HER2-negative clones persist," said Dr. Mittendorf. "Alternatively, we're hypothesizing that this could represent a possible mechanism of resistance to trastuzumab therapy."
She added that, "consideration should be given to reassessing HER2 status in the residual tumor of patients, who do not achieve a pathologic complete response, in order to identify those patients that could be enrolled in a clinical trial to further investigate the most appropriate adjuvant therapy for this population."
The researchers reported that they had no significant financial relationships to disclose.
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Old 10-08-2008, 05:56 PM   #2
Faith in Him
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Help

I believe that I may be one of the unfortunate people who became her2 neg after treatment with herceptin. I was strongly positive at the beginning of all this. Then when I recurred and was triple neg. My onc still considers me positive and I still get herceptin but I wonder if it is doing me any good.

Any ideas anyone?

Tonya
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DX 02/01/07
2.5 cm, Er/Pr-, Her2+++
18/20 Nodes
03/07 CT & Bone scan - Clear
AC x 4, Taxol x 4, Added Herceptin
Radiation until 09/07
Herceptin every 3 weeks until 06/08
01/10/08 local recurrence -IBC
01/28/08 CT & Brain MRI - clear
02/08 - Navelbine & Herceptin
05/08 -MRM
05/08 - Gemzar & Herceptin - didn't work
09/08 - Hyperthermia rads
03/09 - Tykerb/Xeloda
05/10 - Tram flap to fix wound
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Old 10-08-2008, 06:24 PM   #3
Rich66
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U'm not sure being her2 negative is necessarrily a negative considering being positve has the higher risk attached to it. Although..starting to see whispers of Herceptin having utility in her2 negative settings too.
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Old 10-08-2008, 06:54 PM   #4
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I have worried about the same thing, Tonya - when we found my first recurrence, we found that my ER+ status at initial dx was now negative. It's fuzzy territory, because I think I have learned that different recurrences can be ER+ and ER-. I've also learned that a single given tumor can have both ER+ and ER- aspects to it.

That being said, I have worried that if my HER2 status were reversed to HER2 negative, and were it true that I am more ER/PR- than +, then I could also potentially someday be triple negative. YUCK. It's all so fuzzy...

But this brings up great questions for SABCS... I hope there will be some talks there about this gray area.

Rich - it is considered somewhat preferable these days to be HER2 as opposed to triple negative. HER2 is a target that can treated with Herceptin and Tykerb. ER+ is a target that can be treated with Tamoxifen or AIs. --- triple negative has no distiguishable targets and is harder to treat, outside of conventional chemo.
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NOV 2012 - 9 yr anniversary
JULY 2012 - 7 yr anniversary stage IV (of 50...)

Nov'03~ dX stage 2B
Dec'03~
Rt side mastectomy, Her2+, ER/PR+, 10 nodes out, one node positive
Jan'04~
Taxotere/Adria/Cytoxan x 6, NED, no Rads, Tamox. 1 year, Arimadex 3 mo., NED 14 mo.
Sept'05~
micro mets lungs/chest nodes/underarm node, Switched to Aromasin, T/C/H x 7, NED 6 months - Herceptin only
Aug'06~
micro mets chest nodes, & bone spot @ C3 neck, Added Taxol to Herceptin
Feb'07~ Genetic testing, BRCA 1&2 neg

Apr'07~
MRI - two 9mm brain mets & 5 punctates, new left chest met, & small increase of bone spot C3 neck, Stopped Aromasin
May'07~
Started Tykerb/Xeloda, no WBR for now
June'07~
MRI - stable brain mets, no new mets, 9mm spots less enhanced, CA15.3 down 45.5 to 9.3 in 10 wks, Ty/Xel working magic!
Aug'07~
MRI - brain mets shrunk half, NO NEW BRAIN METS!!, TMs stable @ 9.2
Oct'07~
PET/CT & MRI show NED
Apr'08~
scans still show NED in the head, small bone spot on right iliac crest (rear pelvic bone)
Sept'08~
MRI shows activity in brain mets, completed 5 fractions/5 consecutive days of IMRT to zap the pesky buggers
Oct'08~
dropped Xeloda, switched to tri-weekly Herceptin in combo with Tykerb, extend to tri-monthly Zometa infusion
Dec'08~
Brain MRI- 4 spots reduced to punctate size, large spot shrunk by 3mm, CT of torso clear/pelvis spot stable
June'09~
new 3-4mm left cerrebellar spot zapped with IMRT targeted rads
Sept'09~
new 6mm & 1 cm spots in pituitary/optic chiasm area. Rx= 25 days of 3D conformal fractionated targeted IMRT to the tumors.
Oct'09~
25 days of low dose 3D conformal fractionated targeted IMRT to the bone mets spot on rt. iliac crest that have been watching for 2 years. Added daily Aromasin back into treatment regimen.
Apr'10~ Brain MRI clear! But, see new small spot on adrenal gland. Change from Aromasin back to Tamoxifen.
June'10~ Tumor markers (CA15.3) dropped from 37 to 23 after one month on Tamoxifen. Continue to monitor adrenal gland spot. Remain on Tykerb/Herceptin/Tamoxifen.
Nov'10~ Radiate positive mediastinal node that was pressing on recurrent laryngeal nerve, causing paralyzed larynx and a funny voice.
Jan'11~ MRI shows possible activity or perhaps just scar tissue/necrotic increase on 3 previously treated brain spots and a pituitary spot. 5 days of IMRT on 4 spots.
Feb'11~ Enrolled in T-DM1 EAP in Denver, first treatment March 25, 2011.
Mar'11~ Finally started T-DM1 EAP in Denver at Rocky Mountain Cancer Center/Rose on Mar. 25... hallelujah.

"I would rather be anecdotally alive than statistically dead."
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