Pleomorphic ILC

Gitane
Gitane Member Posts: 1,885
Pleomorphic ILC
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  • Gitane
    Gitane Member Posts: 1,885
    edited February 2008

    Are there any other pleomorphic ILC's out there? I'd love to know who we are, what our experiences have been, and especially want to know any survival stories.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited February 2008

    Gitane--my mom had ILC, negative nodes. I don't know if it was pleomorphic or not, but she is now a survivor of over 21 years without a recurrence! (had lumpectomy, rads, tamox). Her story inspires me and I hope it will you  too.

  • am2300
    am2300 Member Posts: 4
    edited February 2008

    Gitane,

    My mom was diagnosed Feb 2007 with stage 2b pleomorphic ILC.  She has finished initial treatments and is now on Femara and doing great.  I read info about pleomorphic ILC online that really scared me, but all the articles/studies were small and really old.  I've been told by an oncologist that pleomorphic is not an established independent poor prognostic indicator.  It seems difficult to find any recent info on pleomorphic... hopefully that means it truly isn't a concern with newer, improved treatment options?  Nash has really researched the pleomorphic issue and is a wealth of info.  I'd love to hear more survivor stories of pleomorphics as well. 

  • Gitane
    Gitane Member Posts: 1,885
    edited February 2008

    am2300,

    Thank you so much for responding. Your mom and I have a diagnosis in common. Please tell her I wish her the best and please keep us posted.

  • Gitane
    Gitane Member Posts: 1,885
    edited February 2008

    awb,



    21 years. Wow! That is fantastic. Thanks for sharing.

  • IllinoisNancy
    IllinoisNancy Member Posts: 722
    edited February 2008

    Hi,

    My cancer is ILC pleomorphic also.  I was diagnosed on 10/06 and had a lumpectomy and SNB which revealed clear nodes.  I also had the Oncotypedx test and received a 9.  My oncologist and breast surgeon all told me not to worry about the pleomorphic term.  It is much more important that it is stage I and ER+.  I had radiation and now on Tamoxifen. I will be for 2 years and then I will switch to Armidex for 5 years.  Good luck with your journey!

    Nancy

  • nash
    nash Member Posts: 2,600
    edited February 2008

    Hi, girls. I will post info I've read on pleomorphic when I have a chance. Just wanted to let you know I saw the thread. Will get back to you all soon.

  • Gitane
    Gitane Member Posts: 1,885
    edited February 2008

    IllinoisNancy,

    I appreciate you posting this. You are the very first person I know of who has pleomorphic ILC and PgR negative BC like mine. Of course, mine was a much later stage, 2b, large tumor, 1 micromet and some ITC's to nodes, so I have a different prognosis, I'm sure. Still, knowing that you can get an OncoDx score of 9 with a pleomorphic ILC is interesting. I hope you will continue to post, I'd love to know you are doing well.



    Nash,

    I would love to read anything you can find. Thank you for the offer.

  • am2300
    am2300 Member Posts: 4
    edited February 2008

    Gitane,

    What are ITC's to nodes?

  • IllinoisNancy
    IllinoisNancy Member Posts: 722
    edited February 2008

    Hi,

    I will continue to keep you posted.  I think that we have a very bright future and we should enjoy each day.

    Take care,

    Nancy

  • Gitane
    Gitane Member Posts: 1,885
    edited February 2008

    ITC's are individual tumor cells. This refers to individual tumor cells in the node or tiny clusters < .2mm that are under the requirement for a micrometastasis. At least I think that's what they are. For me they were found in 2 nodes and one micromet of about 1mm in one node. They were found with keratin staining.

  • am2300
    am2300 Member Posts: 4
    edited February 2008

    Thanks Gitane.  That's a new term for me. 

  • NancyNY
    NancyNY Member Posts: 67
    edited February 2008

    Hi Gitane,

    I'm one of the many Nancy's who seem to have lobular breast cancer.  I was diagnosed in May 2004 both pleomorphic and classical.  I was stage 2A because of size, no nodes involved.  Every doctor I had, including the 2nd opinion from Sloane kettering said that pleomorphic cells donot change the prognosis.  I'm almost 4 years out and so far so good.  Nancy

  • Gitane
    Gitane Member Posts: 1,885
    edited February 2008

    NancyNY,



    What a pleasure to hear from you. 4 years! I'm encouraged by this, I can't tell you. Thank you for sharing this. I'm also glad to hear you were told by Sloane that it doesn't change the prognosis. I was told by my onc that it changes how I respond to chemo, hopefully for the better. I did have a good response to AC, but not a pCR. I wanted to get an OncoDX done to see my RS but my onc discouraged this. He told me it would be intermediate to high grade. I'm assuming he feels this way because it's progesterone negative; I guess I should ask. I didn't know the median RS for pleomorphic then. I read a study posted on the Onco DX site that the median RS for pleomorphic (about 180 cases studied) was 18.9 with a range from 1-71. I guess my onc feels I am above the median recurrence risk. Thinking about this changes nothing, of course, but it's like wiggling a loose tooth as a child, I don't seem to be able to avoid doing the research.

  • nash
    nash Member Posts: 2,600
    edited February 2008

    I'm going to post the links to some of the journal articles I have about pleomorphic ILC. A word of warning--they are overwhelmingly negative. The slant of the articles is opposite what pretty much all of us have been told about our pleomorphic ILC. I think we all have been told that the pleomorphism doesn't change the prognosis, and that what's important is what is important to any bc, namely tumor size, hormonal receptor status, HER2 status and lymph node status.

    That being said, I think it is generally accepted that pleomorphic ILC is more aggressive than classical ILC. However, it is unclear whether all pleomorphic ILC cases are more aggressive, or only those cases that are HER2 positive.

    And given what a crap shoot bc can be, the prognostic indicators are not always relevant. I know women who have classical ILC, grade 1, who also have mets. I know of women with negative nodes who have mets. I also know a woman who had IBC who only had a mastectomy, no chemo or rads, and is fine 13 years later. I have had more than one onc tell me, "Sometimes the women we think will do fine don't do well, and the ones we think will die soon, do great."

    So I think what we can take away from the articles is that exactly what I and others have been told--that pleomorphic ILC is probably more aggressive than classical ILC in general, but no more aggressive than a typical high grade IDC (although I find that confusing, as my pleomorphic ILC was graded a 2).

    Also, the mitotic score of the tumor is important (mine was a 1), because it is probably the best indicator of how fast the tumor grows. So even if one ends up with mets, they too will grow relatively slowly and can be controlled for quite some time.

    Also, the difference in oncotype scores just off of this thread may illustrate how complex the whole situation is--Illinois Nancy's score was a 9, mine was an 18, both with pleomorphic ILC. So, everyone's personal genetic makeup comes into play as well.

    Unfortunately, there just isn't that much clinical interest in pleomorphic ILC. MDAnderson is the only cancer center who pays much attention to it. And I know of a Stage IV pleomorphic gal who recently saw Dr. Christofanilli at MDA (who is probably the most expert ILC onc in the USA), and she said he didn't focus much on the pleomorphic subtype. On the other hand, she's stage IV, so maybe it's moot.

    At any rate, here are the articles--like I said, don't let them scare you. Most of the studies are old and small. But for those of you who like to read what's in the literature on your disease, I wanted to make them available.

    http://www.ncbi.nlm.nih.gov/sites/entrez?holding=npg&cmd=Retrieve&db=PubMed&list_uids=11117786&dopt=Abstract

    (from 2000)

    http://www.ncbi.nlm.nih.gov/sites/entrez?holding=npg&cmd=Retrieve&db=PubMed&list_uids=9758360&dopt=Abstract

    (this is an old one from 1998)

    http://www.ncbi.nlm.nih.gov/sites/entrez?holding=npg&cmd=Retrieve&db=PubMed&list_uids=1398644&dopt=Abstract

    (also, old--1992)

    http://www.ncbi.nlm.nih.gov/sites/entrez?holding=npg&cmd=Retrieve&db=PubMed&list_uids=1592388&dopt=Abstract

    (1992)

     http://www.blackwell-synergy.com/links/doi/10.1046/j.1365-2559.2000.00810.x

    (2000)

    http://www.blackwell-synergy.com/links/doi/10.1046/j.1365-2559.2001.01252.x

    (2001)

    http://www.breakthrough.org.uk/researchcentre/research_groups/molecular_pathology/projects/classic_and.html

    http://www.turkjcancer.org/text.php3?id=45

    (2001)

    http://www.ihop-net.org/UniPub/iHOP/pm/7296306.html?pmid=1398644

    (1992--this might be duplicate info)

  • Gitane
    Gitane Member Posts: 1,885
    edited February 2008

    Nash,



    I've read many articles, but I don't know which of these I've read, so I will certainly use these links. With this PILC we may be able to help one another by sharing, as the information is so difficult to get and in some cases hard to understand. Your work here will help me, I'm sure. I can't thank you enough to taking the time to research and post this. Wow.

  • IllinoisNancy
    IllinoisNancy Member Posts: 722
    edited February 2008

     Q:  

    I need information on PLEOMORPHIC lobular cancer. I have been told by my oncologist that this is "more aggressive" than classic lobular. All the information about cancer that I have researched says the same in so many words with no specifics. Prognostic tables primarily are basing projections on ductal and classic lobular patients since PLEOMORPHIC lobular is so much more rare. I need information on my type of cancer beyond the brief two or three sentences in most books and articles. Where can I get it?

     

    A:  

    PLEOMORPHIC is a term to describe cell shape and not a descriptor for lobular cancer per se. i think you are seeking information on something that doesn't exist.

    My mom is 61 and has stage 2B Invasive Lobular Carcinoma in the right breast with a 3cm tumor and with 3 (of 33) lymph nodes positive for cancer. She is ER +90 and PR +80 and Her2 +1 (considered her2 negative). The nuclear grade is 3 and it says her ILC is PLEOMORPHIC type. Her overall Nottingham Score is 7, grade 2. I've found several articles, mostly over 10 years old, that describe the outcome of PLEOMORPHIC ILC as very bad with high mortality in the groups studied in the article. One even mentioned average death after diagnosis was only 2.1 years. However, my husband works at a hospital and was told by an oncologist that PLEOMORPHIC ILC is not an established poor prognostic indicator and that Mom's 10 yr risk of recurrence after surgery, chemo, and hormone therapy is 25-30% chance. So, I'm confused because the articles I've found seem so much more dismal than what my husband was told. Is the oncologist correct and there have just been great improvements in treating PLEOMORPHIC ILC in the past 10+ years, or is Mom's situation really bad? We live several hours from her, so I haven't been able to talk to her oncologist and don't want to scare Mom with the articles I've found. But, I'm scared and confused myself after what I've read.

     

    A:  

    her having PLEOMORPHIC findings are not an issue. having 3 positive nodes are. the good news is that she has a well behaved breast cancer based on the ER/PR and Her2neu receptors. risk of recurrence is greatest during the first 2 years after treatment is completed. hopefully she will be doing surgery, chemo, radiation and hormonal therapy.

    Q:  

    Hi: I have read studies that say a PLEOMORPHIC lobular carcinoma has a worse prognosis than ductal. If a PLEOMORPHIC lobular was invasive, and her/2 negative and ER positive, would that necessarily be the case? Also one node was involved. Thank you.

     

    A:  

    we focus more on the prognostic factors and yours are very favorable-- hormone receptor positive and her2neu negative.

    These questions were on the John Hopkins Breast Cancer Forum.  They agree with my surgeon and Oncologist that pleomophic is not necessarily a bad thing.  Other factors are much more important.  We Pleomorphics just need to relax:)
  • Gitane
    Gitane Member Posts: 1,885
    edited February 2008

    First, let me tell you that I am very happy you, Illinois Nancy, Nash, and others are reading this thread and have taken the time to post the information. It means a lot to me that you did this.



    Since Ms Shockney is affiliated with this web site, and I find this web site wonderful, I'm torn about posting my thoughts on the answers she gave. But my emotions run deep, so here goes...



    "Ask the Expert" provided a badly needed service. The answers to our questions about pleomorphic lobular cancer are appropriate to the service she provided, but I had hoped for more. Indeed, the first question in your list is mine.



    Pleomorphic lobular is a poorly understood variant of lobular which is a poorly understood phenotype of BC in general. Just like ductal, tumor size and/or nodal status are important. But the same biomarkers and indicators don't always act the same way in lobular or pleomorphic lobular carcinoma as they do in ductal. There is much more to pleomorphic lobular carcinoma than just the nuclear pleomorphism. Researchers are trying to find reasons for its behavior. HER2+ seems to come up as a reason for its being aggressive, but how many are HER2+? Mine isn't. My tumor was VEGF + which is rare in lobular but perhaps not in pleomorphic lobular. Our stats parallel high grade ductal according to some, Stanford feels they parallel grade 2 ductal.



    Ms. Shockney is correct in saying that the answer to my question doesn't exist. But, there is certainly a lot more information available about pleomorphic lobular. The information is just very hard to find because pleomorphic lobular is so much more rare and less studied than ductal. There are lots of variables here, as the Onco DX variance of 1 to 71 in the RS score demonstrates. I just want to find out all I can about what is known about the variables. Don't ask me why I want to do this, as it doesn't seem to matter to me personally, as far as my treatment options go. Still, I'm driven to search, so I guess I'll continue.

  • am2300
    am2300 Member Posts: 4
    edited February 2008

    Gitane,

    I'm like you and feel the need to find the info.  The 2nd question listed from 'Ask the Expert' was mine.  It seems there are just a few of us seeking the little bit of info that does exist out there and that we keep meeting on these websites.  :) 

  • NancyNY
    NancyNY Member Posts: 67
    edited February 2008

    Did you know that the person who answers the Ask the expert questions (Lillie Shockley) is on the Board of directors of the site?  I guess it's true people keep meeting on all the different boards.

  • nash
    nash Member Posts: 2,600
    edited February 2008

    I, in case y'all didn't notice, am an info junkie. Sealed It gives me a sense of control. And over the years, I've found that the docs don't give you all the info you need, nor do they necessarily pay attention to what could possibly be important details of one's particular case. No one thinks as hard about your situation as yourself and/or your family members.

    I'm only 39, I have a 6 year old and a 9 year old, my mother just died of bc eleven days ago, and I've lost my dad, my grandfather and my father-in-law to cancer as well. So dying from the disease is heavy on my mind. I would like to live long enough to see my children graduate from high school.  Perhaps it's a non-issue and I'll live to 100. Who knows. But I like to be realistic and pragmatic, and also like to take a very clinical approach to educating myself about my disease, especially when the docs really don't know much about it themselves.

    And as much as I like Lillie and immensely respect the work that she does, the answer she gave to Gitane's question above was contrary to what's in the literature.

  • Gitane
    Gitane Member Posts: 1,885
    edited February 2008

    Nash,

    I hate breast cancer. I hate that your mother has died of this, that you have it, too, that I have it, that my child might have it in her lifetime, that one in seven women are diagnosed with it and live in this horrible limbo that we must somehow navigate, that remains a shadow in our hearts, and hurts our loved ones as well. My heart goes out to you in your loss. I wish there were better words of comfort, but if there are, I don't know them. Just know that I care. We are all sisters in this.

    Gitane

  • nash
    nash Member Posts: 2,600
    edited February 2008

    Thank you, Gitane.

  • snicklefritz
    snicklefritz Member Posts: 66
    edited February 2008

    Hello ladies:

         Long-time member here but I rarely post.  When I saw this thread I felt I had to put my two cents in.   I am a four year survivor of pleomorphic lobular, very aggressive.  Early 2004, I did the four months of chemo then the radiation.  The reason for my post is that I am doing fine.  I know how frightening it is to look at those studies on pleomorphic lobular.  One day, I read the original study and I got literally sick to my stomach and could not stop shaking for hours.  My oncologist however, allayed my fears by telling me that pleomorphic lobular is NOT any worse than your average, garden variety ductal.  The lymph node infiltration and her/2 status are much more important than the grade or type of the tumor.  My tumor did infiltrate a node or two.  No-one knows for sure why some women do well with certain cancers and others don't.  There is no rhyme or reason here.  Always stay positive and live life to the fullest and try not to get caught up in the studies you read because YOU are your own case and those studies don't involve you.  The other thing is that todays treatments are so much better than even five years ago. 

    Have a great day

    Mary Jane

  • nash
    nash Member Posts: 2,600
    edited March 2008

    Thanks for your post, Mary Jane. And I love your posting name, BTW! It's great to hear how well you're doing.

  • Gitane
    Gitane Member Posts: 1,885
    edited March 2008

    Mary Jane,

    Fantastic that you are going strong. Thank you for posting and cheering me up considerably. Knowing others with a similar diagnosis are doing fine really helps more than anything.

  • pepperpot
    pepperpot Member Posts: 9
    edited March 2008

    Hello,have only just joined so hope I do this right.I was diagnosed with pleomorphic infiltrating lobular cancer,may 06, aged 44 am currently N.E.D.and am doing just fine,so I hope this encourages others ,I was grade 3,er+ and pr+ her2+, node negative,(never did get to know stage,must ask oncologist at next visit)great to know am not alone, as no one I know has ever heard of this type ,good luck to you all,and best wishes to everyone,take care,onwards and upwards,Pepper .

  • nash
    nash Member Posts: 2,600
    edited March 2008

    Hi, Pepper, and welcome! Glad to hear you're doing so well.

  • Gitane
    Gitane Member Posts: 1,885
    edited March 2008

    Pepper,

    There are so few of us pleomorphic ILC's, it's always wonderful to know one who is doing well. Thank you for sharing with us.





  • AnnBrown
    AnnBrown Member Posts: 10
    edited April 2008

    I am a longtime member, also a PLC.  I was diagnosed in August of 04 and had 4 FEC then 4 Taxotere, then bilateral mast w/o reconstruction, then 37 rads, now on tamoxifen.  I am ER+/PR+, grade III, aneuploid, with a very high mitotic count in the original pathology, and now postmenopausal from chemo(I was 45 at dx).  I tried arimidex at the end of rads, but couldn't tolerate the arthritis.  My onc switched me to tamoxifen, and I have pledged to endure it for the full 5 years.  I had 3 positive nodes at surgery.  They could only find 4 nodes total, and my BS figured the chemo had eradicated a lot of nodes that were probably cancerous, too.  Anyway, I'm doing great and really concentrating on having a wonderful life.  At times, I do think about the poor prognosis.  I never asked about prognosis until I was finished with chemo and rads, and then he gave me about a 50% chance of recurrence after all I had done.  I figure that worrying about it doesn't help me or my family, so I try not to.  However, that's easier said than done whenever some new pain crops up.  I am better now about waiting a week or two to see if it goes away.  My onc says cancer pain usually won't go away, so I try to use that as a guide.  He will check anything out, though, if that will give me peace of mind. 

    Anyway......there is life after treatment.  I feel and look normal now, although that did take a while.

    I'll be praying for all of you, my PLC sisters.  We are an elite group!

    Ann

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