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Old 09-24-2007, 10:02 AM   #1
Lani
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circulating tumor cells as risk factor --in patients with early bc (stage 1-3)

Cancer cells in blood can identify risk of recurrence in breast cancer [News-Medical.Net]
Cancer cells circulating in the blood, or circulating tumour cells (CTCs), are known to be associated with a bad prognosis in women with metastatic breast cancer. Now, for the first time, a group of scientists have shown that they can also detect CTCs before and after chemotherapy treatment and hence may be able to identify those patients likely to have a recurrence of their cancer after such treatment in future.
Dr. Julia Rack, from the University of Munich, Munich, Germany, told a press conference at the European Cancer Conference (ECCO 14) today (Monday September 24) that the results could help improve the design of trials of chemotherapy in breast cancer, as well as reducing costs to health services.
The team, led by Dr. Brigitte Rack, also from Munich, set out to look at the role of CTCs in blood at the first diagnosis of breast cancer and during adjuvant chemotherapy and endocrine treatment. They analysed blood samples from 1,767 node-positive and high-risk node-negative breast cancer patients before the start of their treatment, and compared the results to those obtained from 852 of the same patients after completion of chemotherapy.
"We found that 10% of patients whose blood was sampled before the start of treatment had more than one CTC, and 5% of these patients had more than two CTCs in approximately 20 ml of blood," said Dr. Rack. The presence of CTCs did not correlate with other prognostic factors such as tumour size, grading, hormonal or Her-2 status, but the scientists did see a significant correlation with the presence of lymph node metastases.
Of 24 healthy individuals used as controls, none showed more than one CTC, said the scientists. Among the 852 patients whose blood was analysed post-treatment, 11% were CTC positive before the start of treatment, while 7% had more than one CTC after completion of chemotherapy.
Of those patients who were initially CTC positive, 10% remained so and 90% had a negative CTC test after chemotherapy. Of those initially CTC negative, 93% remained negative, whereas 7% had a positive CTC result.
The advantage of screening for CTCs is that, unlike other predictive factors, including genetic signatures, it can be carried out after the completion of primary therapy, and, if needed, on other occasions during the duration of disease. Other predictive methods can only be used on diagnosis, and only once, say the scientists.

ABSTRACT: Circulating tumor cells (CTCs) in peripheral blood of primary breast cancer patients - Results from the translational research program of the German SUCCESS-Trial [European Cancer Organization]
Background: In metastatic breast cancer, the presence of CTCs has been shown to be associated with bad prognosis and their persistence predicted lack of treatment efficacy. Only limited data, however, has been published in the adjuvant setting. We evaluated the role of CTCs in peripheral blood at primary diagnosis and during adjuvant chemotherapy, endocrine and bisphosphonate treatment within the SUCCESS-trial (n = 3658 pts.)
Methods: We analyzed methods of 23 ml of peripheral blood from 1767 N+ and high risk N- primary breast cancer patients before systemic treatment. 852 of these patients have undergone follow-up blood sampling after completion of chemotherapy. The presence of CTCs was assessed with the CellSearch System (Veridex, Warren, USA). Briefly, after immunomagnetic enrichment with an anti-Epcam-antibody, cells were labeled with anticytokeratin (8, 18, 19) and anti-CD45 antibodies to distinguish epithelial cells and leukocytes.
Results: 10% of pts with a blood sampling before systemic treatment (n = 170) showed >1CTC before the start of systemic treatment (mean 13, range 2-827). While we found 2 CTCs in 5% of patients, 3% had 3-5 CTCs and 1% 6-10 and >10 CTCs each. The presence of CTCs did not correlate with tumor size (p = 0.07), grading (p = 0.30), hormonal status (p = 0.54) or Her2-Status of the primary tumor (p = 0.26). However, we observed a significant correlation with the presence of lymph node metastases (p = 0.015). None of 24 healthy individuals showed more than 1 CTC. Among those 852 patients with follow-up blood sampling after the completion of cytostatic treatment, 11% were CTC positive before starting systemic treatment (mean 7, range 2-166), while 7% of patients presented with >1CTC after completion of chemotherapy (mean 6, range 2-84). Of those, initially CTC positive, 10% remained positive (n = 9) and 90% had a negative CTC test after chemotherapy (n = 82). Of those initially CTC negative, 93% remained negative (n = 711), whereas 7% returned with a positive CTC test (n = 50) (p = 0.24).
Conclusions: The SUCCESS-trial is the first trial to perform the detection of CTCs in a large number of primary breast cancer patients with this highly standardized and easily applicable approach. If the observed persistence of CTCs after completion of adjuvant chemotherapy is prognostically relevant, will have be further evaluated with longer follow-up.
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Old 09-25-2007, 06:03 AM   #2
Lani
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more .....reasons to eat your tomatoes and carrots!(and avoid soy)

http://www.reuters.com/article/healt...88917420070924
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Old 09-25-2007, 06:04 AM   #3
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more ....

http://www.reuters.com/article/healt...88917420070924
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Old 09-25-2007, 09:45 AM   #4
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Are CTCs and Tumor Markers the same thing?
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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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Old 09-25-2007, 10:04 AM   #5
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They are not the same.

A circulating tumor cell (CTC) is exactly what you think - a breast cancer cell in the bloodstream.

Tumor marker (let's say CA 27/29) measure the amount of a certain protein. Tumors produce more of this protein that normal cells (and/or organs). So, when tumors are growing and getting bigger (or spreading), more of the protein is being produced and the "tumor marker" goes up and can be measured in the blood. (This is kind of like being pregnant. You don't do an ultrasound to try to find a tiny object but you can measure the amount of pregnancy protein (in this case, HCG) in urine).
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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 09-25-2007, 01:29 PM   #6
lilyecuadorian
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Becky thanks for explanation ..you are a really good teacher for me ...My husband know about you ...because I always said " oh Becky think this or that etc"
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Diag April/06 5 months after give birth my son Max
stage IV mets on liver (5 tumors) 38 year old,
her2+++ and ER+PR+ from32 nodes 4 positives
mastectomy right breast chemo before surgery herceptin/carboplatin/taxotere ,clear and surgery have radiation 20, `& then herceptin and tamoxifen
NED until Aug/07 body only then 'n June 04-06-07 .1 lesion of 1.6 cm on cerebellum ...novalis ,open sugery
5m.m brain met again novalis, 4mm.In the liver. Waiting 2 months now 3 tumors enroll on T-MCC trial start first infusion Nov 5/07 at Dec 17 scan show one tumor despair the 2nd and 3th diminish Doc said great results until March/08 ct scan show progression
03-05-08 start tykerb & xeloda
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Old 09-25-2007, 11:24 PM   #7
harrie
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Have any of you been tested for CTCs before and/or after chemo?
If CTC is in the bloodstream, in very small numbers, I would presume it may not be enough to elevate the scores of the markers. But I would assume it would be valuable information to know if there are CTC present even in small numbers.
Your opinions please....
Maryanne
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*** MARYANNE *** aka HARRIECANARIE

1993: right side DCIS, lumpectomy, rads
1999: left side DCIS, lumpectomy, rads, tamoxifen

2006:
BRCA 2 positive
Stage I, invasive DCIS (6mm x 5mm)
Grade: intermediate
sentinal node biopsy: neg
HER2/neu amplified 4.7
ER+/PR+
TOPO II neg
Oncotype dx 20
Bilat mastectomy with DIEP flap reconstruction
oophorectomy

2007:
6 cycles TCH (taxotere, carboplatin, herceptin)
finished 1 yr herceptin 05/07
Arimidex, stopped after almost 1 yr
Femara
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Old 09-27-2007, 05:25 AM   #8
BonnieR
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I am getting confused about this issue too. And have chemo brain on top of it! Anyway at my onc visit yesterday i tried to ask why I am not receiving the HER2Serum blood test that I have read about on this board, I was told not everything does not apply to all patients.
Later I received my CA 27.28 Result which was 30. I know that is low and within "normal range" but it has gotten a tiny bit higher each time. The doctor tried to explain that it is a normal function of the body and that everyone has these markers floating around. I dont understand why, if there is no tumor, why is there a "tumor marker" to begin with? I am thought to be tumor free
I have been awake for awhile fretting and tryin to figure it ouy, My typing os sure suffring chemo brain and steriod effects this morningl Feeling scramblwd. Maybe not the best time to be lucid.....
but could use input....
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Post menopause
May 2007 Core biopsy, Rt breast
ER+, Pr-, HER2 +++, Grade 3
Ki-67: 90%
"suspicious area" left breast
Bilateral mastectomy, (NED on left) May 2007
Sentinel Node Neg
Stage 1, DCIS with microinvasion, 3 mm, mostly removed during the biopsy....
Femara (discontinued 7/07) Resumed 10/07
OncoType score 36 (July 07)
Began THC 7/26/07 (d/c taxol and carboplatin 10/07)
Began Herceptin alone 10/07
Finished Herceptin July /08
D/C Femara 4/10 (joint pain/trigger thumb!)
5/10 mistakenly dx with lung cancer. Middle rt lobe removed!
Aromasin started 5/10
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