Final study results!!!!!!!
Comments
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Wow--hadn't checked this thread in a few days. Y'all have been busy!
Lindalou--thanks for the info on the abraxane and xeloda in a non-metastastic setting. Nosurrender--didn't mean to freak anyone out--it's just that my mom is Stage IV, and she didn't go on abraxane or xeloda until she had mets. I didn't realize those drugs were used in other instances. Good to know, thanks ladies.
Matic--re: Oncotype DX. Mine took about 2-3 weeks. My score was 18. I had a 2.7 cm pleomorphic ILC, ER/PR+ (50%/30%) HER2 -, grade 2, mitotic 1 tumor. SNB--0/4 nodes. Am doing CAFx6.
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Matic, I know you have mentioned the Oncotype DX many times and have indicated if I am correct that you would like to have your mom's tumor tested. Were your mom's nodes negative? If not, here in the US they normally do not run the test if you have positive nodes. It is my understanding that you can only have the test done if you have ER/PR positive breast cancer and negative nodes. Since I had a positive sentinel node I was not offered the test.
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HI, matic,
Thanks for your comments, and yes, I did understand them (I'm a health care provider.) Having been on Arimidex and Femara for the IDC, I agree that examestane is the choice, if indeed i must choose. I'll see my oncologist Tuesday for this discussion.
Keep up the good work. Seems you have a gift for both research AND people--a rare combo in our medical world at times.
Anne
Anne
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Dear Matic,
It is very good to see you posting again! Thanks for all your research and time devoted to sharing both your knowledge and encouragement with us.

LindaLou
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Phew!!! Matic, I am also glad you are back posting. I see how so many of these women depend on your counsel. Your response to my questions worried me that you would not return for them.
I also read your responses with interest, and now that I understand where they come from it helps put them in the proper perspective for me.
As I said, my prognositic indicators stage 1, mitotic 1 no nodes, no vascular invasion, no necrosis are all good things, but the rarity of ILC triple negative made a adjuvant chemo decision very hard for me. A nationally noted Oncologist in my area recommended TC for me for the very reasons you mentioned. I appreciated you were there to respond to me as well.
Surely now that we have resolved the recent misunderstanding, I will gladly jump back into the discussions where appropriate, but..... still I am direct and I do ask questions. This is not meant as critisim. If this causes problems for anyone... I will of course back out.
warm regards
Grandma Wolf...aka Dakota
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Matic,
I had asked my oncologist about OncoTypeDx. It requires a HR+, so it wasn't useful for me, I don't think there are any other restrictions though. However, there is another service called Adjuvant on line. Would this help you? I think it may only be available to people in the medical field, so you might access it directly yourself. Hope this might help. Grandma Wolf https://www.adjuvantonline.com/index.jsp
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Welcome back GrandmaWolf! Asking questions is what these forums are all about....so please don't hold back!

P.S. you are correct that adjuvantonline is designed for medical professionals. There is another similar site however that I heard recently recommended in another post here. It allows access to anyone. I think the statistical outcomes produced on that site are slightly more favorable than the ones on Adjuvantonline so it has now become my favorite! It still is important to mention that no Breast Cancer Outcomes Calculator can account for each of our unique pathologies. They serve only to show the relationship of general tumor pathology and treatment protocols to predicted survival.
You can check it out here.
http://www.cancer-math.net/breastcancer/~With%20Therapy/
LindaLou
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I've been away on vacation and wow lots has been going on since i last checked in. Matic ....you have been so helpful, inspirational and have given me hope in battling this disease. I appreciate your passion in researching ILC and your willingness to sure your knowledge. I have access to medical journal as I'm a health care provider but do not at time have the medical knowledge to clearly understand everything I'm reading. You have been a wonderful resource when I need clarification. Grandma ...I'm relieved to see you have continued to respond. These boards offer such support and we all have so much to offer one another. Mo
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According to the calculator, I get an extra 80 days if I do Tamox. or AIs. The benefit for me still seems to be really low, but I think that I'll still make an onc. appt. for extra, extra peace of mind.
Thanks for the link LindaLou
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Lini57,
You probably already knew this but let me point out just a few finer points of this calculator if it helps to understand your results and if they are entered accurately.
First off the calculator uses millimeters for tumor size, not centimeters. For those of us with tumors over 1.0 cm you have to remember to convert to mm. My 5.1cm tumor has to be entered as 51mm. It will make a difference if not entered correctly.
The calculator is one of the few that will show statistical differences between the type of BC you had, whether it was Ductal, Lobular, mixed types or many of the other less common BC types. It also distinguishes between ER/PR+ or ER+/PR- etc.
Once you have your actual age and tumor characteristics entered, there are 3 statistics that should not change. The statistic for 15 year death rate without adjuvant therapy, average life expectancy of women without breast cancer and how much that average life expectancy would change for someone with your age and tumor characteristics without taking adjuvant therapy.
Then you can play around with the Adjuvant Therapy options to see how they impact the 15 year death rate with adjuvant therapy, and how much the average life expectancy without adjuvant therapy can be extended by using various adjuvant therapies.
In my case, by adding Aromasin for 5 years to my already 3rd generation chemotherapy, I can reduce my 15 year death rate by 15% and add 1432 days. If I had opted for no adjuvant therapies at all my 15 year death rate would jump from 30% to 82% and my life expectancy would be cut by 22 years
I find it interesting to play around with the tumor characteristic stats also just to see the impact of a larger or smaller tumor size, number of nodes involved or differences between cancer types. It helps to see how many of our pathology stats are interconnected.
I still have to reiterate with EMPHASIS however, that while these types of tools may help give us a better understanding of how certain therapies can benefit us, they are NO SUBSTITUTE for sitting down with your onc and discussing the specific pathologies and characteristics involved in your BC. No calculator can possibly take into account all the nuances of each of our individual BC presentations.
With that understanding, my research/analytically oriented mind enjoys playing around with these to gain a better understanding of how the statistics are generated.

LindaLou
P.S. if you need a centimeter to millimeter conversion the simple rule is to just multiply your cm x 10 to get the mm.
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Thanks, LindaLou - I like this calculator better than adjuvantonline, too. Not only did it give a better outlook, but I like that it separates out lobular and looks for exact tumor size rather than just a range.
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Hello LizM!
Yes, I know that.My Mum has had 2 sentinel nodes positive in the level I of axilla, 2 micrometastases (2 and 1 mm).HOWEVER I believe there is a chance to do oncotype on your own request but of course it is very expensive(I am not sure how much).I spoke to my Mum the other day and she says she would actually like to know these scores but she has just forgotten the cancer.I am glad she does well. I think these gene test of the tumor is more accurate than lymph node status and grade and so on. So then I will know if chemo was suitable for her, especially I am concerned about Epidoxorubicin, which is an anthracycline, that certainly has some toxicity in the body, and I would not give the anthracyclines to favourable tumors, only to tumors that express topoisomerase @2.It is an enzime.Recent studies show many women do not need anthracyclines but rather alkylants such as Cyclophosphamyd with or without a taxane(Docetaxel).
So I have to speak to her pathologist, who I know very well and have to decide about the blocks of her tumor.I would like to have the results in this year already.
I will keep in touch:=)
Matic
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Whew...I am so happy we're all back on track here! I love the fact that you were able to understand each other's confusion - work through it and then move beyond it. Gma and matic - you're both great! Us ILC girls are an "elite"/rare group and it's great that we can stick together and help each other. Thanks for that!
matic -
Hi! I finally found out from my Onc...the pleomorphic of my path. was less than 10% - I think he and you have both said that's considered favorable. The mitosis was not noted on my path, but I got the impression that my Onc. thought that was due to the pleo having been low at 10% - . Does that sound right to you? Say hi to Mum! Hope all is well.
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Dear LauraGTO!
Hi!!Well it is hard to say why there is no mitotic scores, because usually there are in every paht report.I do not know whay not in your case. The good thing is that pleomorphic features were less than 10%.That is good!We do not like pleomorphics;)BUT I have to say also our best pathologist in Slovenian Institute of Oncology in Ljubljana said to me she does not believe pleomorphic lobular really goes worse than classical or any other lobulars. I have to admitt I can not say yes or no to this statement because nobody has done in our country that research.Next year or later on I WILL DO the work on lobulars and I will compare classical lobular to pleomorphic lobular and to ductal carcinoma of breast and then I will be able to say the conclusions of those specific patients.
we will see.My idea is if pleomorphic lobular still has ER,PR+++ and HER-2- markers and low mitotis rate, it still is favorable but I also believe there are some other genes expressed within this tumour because there is something to make it PLEOMORPHIC, so the cells ar larger and have large nucleuses, so there is something that has to do with this differentiation into the more pleomorphic way.
I am sure I will figure this out in the future, so then it will be easier to treat those patients more aggressively than classical lobular.
Can I ask you which hormonal therapy you are now on?You have had only 1 lymph node positive, havent you?
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I was told at the time of discussing my path report that grading ILC is not necessary since the invasive cells are lazy and well organized (indian file?) No mitosis was mentioned. Is tumor grading and mitosis the same thing? I do remember discussing that the current formula to grade/score tumors can not and should not apply to ILC or if this criteria is used, all ILC would be graded the same because of the lazy tumor. Obviously something has changed in this grading system. Ihad my tumor out in September of 04. What did I miss or what do I need to ask at next oncology appointment. I usually can get these docs angry by my questioning. I clearly get the impression of them thinking "How dare you question me" I have been able to hold my own and try very hard to be non threatening.
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Here's an article that discusses whether ILC should be graded or not (it concludes that it should). I know some labs grade ILC while others don't:
http://www.nature.com/modpathol/journal/v18/n5/full/3800273a.html
Gracejon--mitotis is part of the Bloom Richardson grading system. The tumor is graded on mitotic count, nuclear grade and architectural grade (tubule formation), all on a score of 1 to 3. The 3 sections get added together for a total score, which determines whether the tumor is grade 1, 2 or 3.
Matic--I'm continuously confused by my pleomorphic lobular. It's a grade 2, mitotic 1, but pleomorphic cells are clearly "angrier" looking than classic ILC cells under the microscope. And although I'm ER/PR positive, I'm only moderately so (50%/30%). I'm HER2 neg, but I've read research papers that say pleomorphic lobular can be HER2 positive in as many as 80% of the cases. So, it's not clear from the research what makes pleomorphic ILC more aggressive--is it only the cases that are HER2 positive? I do know of pleomorphic ILC women who are HER2 neg and also Stage IV, so it has to be more than the HER2 issue.
I also have read papers that suggest a genetic compenent to pleomorphic ILC, like you mentioned, Matic. Which would make sense, as I was 38 at diagnosis, with a very strong family history of cancer. I've read research that suggests a BRCA2 tie-in for pleomorphic ILC. I ended up testing BRCA negative, which surprised the docs as I am an Ashkenazi Jew whose father died of pancreatic cancer. The docs think there is probably some BRCA gene that hasn't been discovered yet that's related to BRCA 1 and 2, and that I could have that mutation. Perhaps that ties in to the pleomorphism somehow.
The number of involved lobules on my path report was greater than 10%, which I was told was bad. But then my mitosis was 1. So I feel like a big walking conundrum!
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Matic,
I have been a silent reader of all the ILC discussions until you told me about your mom's prognosis.
I had a bilateral mastectomy, sentinel node biopsy with 6 nodes removed 2 tested positive. One .2mm the other 2 mm. The original tumor was 2.5 cm. ER/PR+ HER- staged at 2b. Mitotic: 1 tumor grade 2. .3cm clear margins. There was NED on the left breast that was removed.. call it collateral damage.
The onc put me on Dose Dense AC then will proceed with Taxol ( despite the outcome of the research showing that Taxol might not do much for HER- gals, he feels I need to do it cause of the + nodes)
Now I am in a bind here. They are pretty much leaving it up to me to:
- go in an remove more nodes - WHICH IREALLY DO NOT WANT !
- Have full axil rads after chemo
I will be consulting some specialists but wanted to see what your mom would be doing since we seem to be almost in the same boat with her. I will be sending my path slides out too.. anything special you would suggest that I ask about ?
I really want to keep my lymph nodes, but my priority is to wipe this out once and for all too..
Presently I have completed 3 out of the 4 AC's.
Thanks !
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Lindalou~ Thanks for the clarification. My tumor was 4mm. I was extremely fortunate that they found a lobular so small. I did input different therapies and outcome only changed by days.
lini
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Nash, thank you. I could not for the life of me remember the name Bloom Richardson confused it with prostate Gleason score. For sure the oncologist said the only scale they believe in is Bloom Richardson and lobulars can not and would not be able to be scaled with that system. I also remember reading about Nottingham. I really have put a lot of this out of my mind so need a refresher course once in awhile. I am ambivalent on information and how it relates to my personal circumstances. I question whether I could or would change anything at this point anyway. I did one of those therapy things recently and kind of forgot that this even affected my expected age of longevity. I was really surprised this knocked off quite a few years. Originally my question to the doctors was how long do I have to live. Now it's more like what me? No way! I have clearly cleaned up my act and am living a far more healthy life style and shoot, it has to catch up with me. Since my friends and family are exhausted trying to keep up, I think I have cards on my side. I do go to a hospital that considers itself tops in it's field. I am glad that they think so but perusing even these threads makes me very skeptical. Again it leads to some lively discussions at times of visits. I even print some of the info and have had the answer of "I don't know where that info came from but I doubt it's validity" I guess it does not endear me to my medical team but I do appreciate some defensive posture instead of discounting these issues,
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Lini,
I was with a woman today who had LCIS. She had a bilateral and recon and that is it. NO AIs or anything.
She is celebrating her 20th YEAR NED this month!
xxoo,
love you,
g
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Thanks, Gina. I decided just today that I'm not going to let it bug me so much anymore. It was invasive, but only 4mm. My bilateral was considered "overkill" by some, so I'm going to relax and quit stressing over it. 20 years will put me at almost 70. That's cool!! I'll start worrying again then. LOL!!
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HooRAy... for you Matic,
I just noticed you filled in your profile. That is so helpful when people just start posting to these boards.
Grandma Wolf..aka Dakota
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Hey Grandma - I love the picture. Just wondering if it is you????
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I'm confused on the topic of pleomorphic ILC. Would this be outright listed in my path report? The only thing related I see is the Nottingham score in which my nuclear pleomorphism is 2. No other mention of this word in the rest of my report. So, do I have classical or pleomorphic ILC??
Thanks!
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Connie--pleomorphic ILC is a subtype of ILC and is different than the nuclear pleomorphism grade. Not all path labs distinguish the subtype of ILC. I had two labs look at my slides, and only one (the university hospital) identified the pleomorhpic ILC. The other lab just called it ILC.
So, yes, it would be on the path report, and mine was under "diagnosis".
Of course, that doesn't really answer the question of whether you have classical or pleomorphic. There'd be no way to know other than have the slides reviewed. Since you're grade 3, there's a good possiblity you are pleomorphic. However, unless it changes the course of treatment, it's probably not worth pursuing.
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HARMONY...with a capitol H! I love it!
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matic - Okay...I'll try to explain this: When I had the core biopsy, my largest tumor (3.9cm) was as hard as a rock! The Radiologist said it was "as hard as a hockey puck". He had to jab it at least 15 times to try to get a "core" of it to biopsy. In doing so, a huge Hematoma developed. When the path came back positive for bc, and a Mast. was required, the bs said the Hematoma was so bad, that I had to wait for it to subside b/4 they could do the Mast. (I had to wait 3 weeks). And then...after the Mast., the bs said she could not visually grade the largest tumor because of the Hematomo, so we had to wait for the final pathology report. So now, I am wondering if the reason there's no mitotic level noted is due to the fact that the tissue was extremely damaged from the Hematoma/trauma of the core biopsy. What do you think? Thanks as always!
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hello matic22
i have ki-67 data (less then 5%)
hr - score 0 (0-3)
i dident get grade data.
astrogen>75%, progestron>75%.
tomur 2cm ILC classical varian.
1)what grade no. to fill on adjuvantonline
2)in the SLN 1 micrometastasis <0.5mm (is it involvment nodes - 12 nodes are clean after second surgary of axillary nodes)
thank you
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Hi Laura,
FYI, my path report does not list mitotic level either. It also doesn't tell me the ER/PR percentages, just that the tumor was ER+/PR+ Very annoying! My slides were also sent to both Dana Farber and Beth Israel in Boston and they didn't list these values either.
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PeggyDixon, to answer your question if that was me in the picture..
Yep Peg, that is me on my mechanical soulmate of almost 20 years. I have been up through the mountains of NewHampshire,down the twisty roads of West Virginia, the beltway into DC...you name it.
When i was on chemo eight years ago feeling like you know what, jumping on that bike and riding like the wind was the only thing that made me feel better. In fact, with the black bike, wearing black leather, sunglass's, big skull earrings and my chemo bald head, I looked like something out of "Natural Born Killers". I got respect at the checkout counters for sure.
Right now I am too preoccupied with my current situation... just dx second primary in opposite with Lobular...only to find highly suspicious areas on the original breast. Folks were always worried I'd kill myself on a motorcycle... not as likely to kill me as these old boobs, I think.
How is your situation currently. Do you notice a different approach to the treatment information talked about on this board and what you experience with the medical community in Canada?
PS: am I the only ditsy one who gets lost on getting around in these conversations? I try to respond to a specific posting and usually go round in circles to get where I want to be....duh.
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dear grandma!
YES, I have already seen adjuvantonline but it does not fit to me because it really is not good.The tumour size, for example, between 2 and 5 cm is taken together, but in clinical practice we can not just take it as both the same prognostic information.Actually the size of the tumour does not matter so much as does biology of the cancer.If I find anything interesting about ILC, i WILL POST.aND PLEASE if any lady has some articles, please be so kind and put it down.There is noone that would know everything.Kind regards;)
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