I need to see an ILC expert
Hi,
After fighting ILC for 11 years, I think cancer is winning. I just underwent surgery for the third time on my breast area. To make this short and to the point, my ILC is spreading throughout my skin. It completely took over my LAT flap and after removal I did not get any clean margins. It is everywhere in my breast skin. I've had as much taken as they could and now it has been found in my stomach skin. I've completed surgeries, chemo, radiation, Tamoxifen, Arimidex and now another hormonal treatment pill. My ILC is always 90+ Estrogen, 0% PR, 0% HER-. I'm really scared that nothing will stop it. Local oncologist don't have an answer. Please help me. I will travel anywhere for treatment.
Thank you,
Nancy
Comments
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So sorry for your situation. Just want to mention to do your research and make sure you choose a university based teaching hospital to be treated. You might even be able to do some research and find somewhere that specializes in ILC, such as Mayo Clinic or the like. IMO where we are treated is a huge piece of this puzzle. Good luck and please keep us posted...
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Why don't you look into the Chicago area?
http://www.chicagobreastcancer.org/site/epage/9367...
Maybe you can be directed to a specialist or you may qualify for new treatment options.
Good luck to you.
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Illinois Nancy, what about MD Anderson Cancer Centers? They have several locations, one in NJ (might be the closest to you), Fl, and one here in Az, too. Can you get a referral from your MO for someone who specifically treats ILC in skin? I'd demand one and go right away wherever they are located. I would think that metro Chi-town area would have some specialist available?
We are here for you and care. Keep us posted.
Claire
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Nancy - I'm so sorry to read this news. I agree with Lekker that University of Pittsburgh may be a good place to start. One of the co-chairman on the ILC conference was from Dana Farber so that may be another place to try.
The link below is to an interesting article about ILC that talks about mutations in local recurrences. I think that there are targeted therapies for PIK3CA mutations that are approved for metastatic BC. I don't know about regional recurrences.
https://breast-cancer-research.biomedcentral.com/articles/10.1186/s13058-015-0519-x
I will be thinking about you as you navigate your way through this newest diagnosis. You've been through so much in the past few years and you have persevered. Sending positive vibes your way.
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This is gut wrenching. I am so sorry you are dealing with this.
Have you checked clinical trials for immuno type vaccines?
If I come across anything, I'll post back here. I always think of you and am saddened by this.
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Very sorry to read this Nancy. The others on this post have some great suggestions. I sincerely hope that you are able to find an excellent treatment centre for ILC. Mine is similar ER 90% PR 5%.
Best wishes to you.
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Nancy, I have never been able to find a medical oncologist who is considered an expert in ILC, but I think the best bet is to go to a NCCN center. In Illinois that is
The Robert H. Lurie Comprehensive Cancer Center of Northwestern University
Chicago, Illinois
Administrative Office: 312.908.5250
Patient Referrals: 866.LURIECC (587.4322)
www.cancer.northwestern.edu -
I could not sleep last night after reading this post. I thought about my neighbor...he has kidney cancer that spread. He is older so not able to do a lot of treatments. They are using Keytruda (pembrolizumab) on him and it has halted his cancer. This is originally used for skin cancers, but Jimmy Carter had this for his melanoma that spread to his brain and stopped the cancer.
I'm also going to copy/paste your post and send it to my oncologist asking if she knows anything; her new hire is the one using the Keytruda on our neighbor.
Hang on...we will try all we can!
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Nancy, the ladies all have excellent suggestions of where to try to get help. Sending gentle hugs. Please keep us posted.
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Re: Wallycat's suggestion of Keytruda, there are some clinical trials going on with Keytruda for breast cancer. One is testing Keytruda with Ibrance and letrozole for hormone-receptor-positive bc. I think this one is at City of Hope and Mayo Clinic, and probably some other locations as well. There is one for TNBC with Keytruda and Halaven. For details you can search for Keytruda here on the discussion board and also on a clinical trial search.
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My onco replied to me this morning. We are in the middle of nowhere--seattle is an hour to a ferry and 1/2 hour on the ferry...so she was speaking about this area but here is her post (I've skipped the sympathies on my recently deceased, unexpected cat horror).
I am also sorry to hear about your cancer-board friend who is fighting ILC recurrence. Sounds like she has had the usual first line endocrine therapies: surgery, radiation, tamoxifen, arimidex.
There has been some advances in treating ER + breast cancer in recent years. There are some active endocrine combinations:
fulvestrant + letrozole
palbociclib + either letrozole or fulvetrant
everolimus + exemestane
fulvestrant alone
I am not aware of any trial that is using immunotherapy for breast cancer at this time but there likely will be in the future.
If she has not discussed with her oncologist, it would be good for her to let them know she would be interested in a clinical trial, and maybe request referral for a second opinion about treatment.
Also, if the cancer is only in the skin (as I interpreted her note) perhaps more superficial radiation might help? If she is not getting treated at a tertiary care center, a second opinion at one (e.g. Seattle Cancer Care Alliance, if she is in this area) might be a good idea. Her situation is not very common, and it is always good to get more people thinking about an unusual problem and they could get a team approach (med onc, surgery, plastic surgery, radiation, etc) to weigh in on best treatment. Perhaps that has already been done?
My best wishes to her!
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Thank you all so much! I don't feel like I'm fighting alone with all of your support. My doctors are trying to get me into the University Of Iowa Hospital at Iowa City. I value all the information you have shared and will follow through with my next doctors.
I love you all!
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Nancy, the ladies here know so much more than I do. I hope their suggestions can help you make treatment decisions. I am holding you in my thoughts and will be checking back here to see how you are doing. Warm hugs going out to you! G.
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Thanks for checking back in Nancy. Please update us if you can after your appointment. We're all hoping that Iowa has the right treatment for you!
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Good luck I hope you can get in a trial that shows promise like keytruda.
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Hi Friends,
Just a quick update on me. I have an appointment to see a specialist in Iowa City on Friday, January 27th. Hopefully I will get my treatment options and start fighting cancer again. Thank you all so much for your continued support. I can't tell you how much it means to me.
Take care,
Nancy
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Good luck Nancy, I hope they have some new treatment for you.
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Great news, Nancy! Keep us posted!
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Well....saw the specialist at Iowa University Hospital, Cancer Department. Doctor was very blunt and to the point. He told me since I have two different cancers that have progressed beyond the primary I am not eligible for any trials in the United States. No one wants someone like me because while they would treat one cancer, the other one could kill me. He thinks I should not have any more surgeries because my ILC is everywhere and it would be like having four flat tires and only changing one. He said radiation would not be helpful either. That was a quote from him. He told me I should just enjoy what is left of my life and take Ibrance along with Aromasin if possible. He cautioned that the FDA and insurance companies have not approved that combination however since I just started Aromasin in October it would be best to keep with it. I may need to combine Ibrance with Faslodex injections which has been approved. Since I already get injections of Sandostatin every 28 days in the butt I would have to alternate those with Faslodex. They are all big injections according to him. He said I should not do any surgical procedures on my liver either since it would just be another blow to my body. He said I have already had more surgeries and treatments than most people. He recommends that I take my hormone treatments and neuroendocrine injections and no more. He didn't think I need to return to the University because the local oncologist is doing everything he would. At least it was worth a try and I now know where I stand. Thanks for hanging in here with me. I appreciate your friendships. I'm glad that none of you have this crazy combination that I have.
Take care,
Nancy
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((((((((((Nancy)))))))))))))))))))
Cancer centers of America in Illinois---have you been there? I would get a second opinion. You may not qualify for any trials, but maybe there's an onco that can do an "off label" treatment that may do something.
I've been thinking about you and grateful you post your updates and situation. I am so deeply sorry you are foisted this hell-of-cancers to contend with.
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Illinois Nancy, I am confused. Are you Stage IV? Your diagnosis section doesn't say. But if you are NOT Stage IV, the information you received is questionable.
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I'm truly sorry you're dealing with this. If you don't mind, I'd like to ask a few questions and provide a different perspective. I don't know your entire situation, so sorry if any of this has been covered.
1. Other than the skin mets, what other mets do you?
Besides ILC, what is your other cancer?
2. I wouldn't give up. I'd get second and third opinions.
3. Have you had any advanced genetic testing to identify your mutations? Some options are:
- FoundationOne by Foundation Medicine
www.foundationone.com
- Guardant360 by Guardant Health
www.guardanthealth.com/guardant360
- GPS Cancer by NantHealth (my recommendation)
http://nanthealth.com/gps-cancer
4. If you've exhausted conventional options, please consider Immuno-Oncology drugs. Yes, Immunotherapies are still very experimental for breast cancer and they are not FDA approved yet. It's a slim chance that they will work. BUT, if they do work, these experimental agents offer "the chance" of generating a durable long term response. Maybe only a low chance, but a real CHANCE. Immunotherapies have revealed impressive responses in a variety of tumor types for which conventional therapies historically have had limited success (melanoma, leukemia, lymphoma, lung, liver, bladder, head & neck cancers, etc). Tumors are heterogeneous and always evolving, so conventional drugs that are designed to kill cancer cells directly by targeting cell-intrinsic pathways inherently select for resistant clones that can lead to relapse. With Immunotherapy, immune cells are like a "living drug", and can generate a coordinated and robust anti-tumor response with capacity for memory, potency and specificity that is not achievable using any other therapeutic modality. Read that last sentence again. It's important to understand this notion.
Immunotherapies can be accessed by enrolling in a Clinical Trial. There are over 250 different immunotherapy trials that are enrolling breast cancer patients throughout North America. Most are Phase 1 trials since breast cancer has historically been considered immunologically silent.
However, enough time has passed where some of these Phase 1 immunotherapy clinical trials have revealed durable responses from a minority of Stage 4 TNBC patients whose metastatic tumors have melted away with Checkpoint Inhibitors (Keytruda, Opdivo, Yervoy), a form of Immunotherapy.
For example, here's a recent success story of a metastatic Triple Negative Breast Cancer (TNBC) patient with Skin metastasis who exhausted all conventional therapies and responded to a Immunotherapy combination.
http://www.cityofhope.org/miracle-patient-finds-new-hope-with-breast-cancer-vaccine?
The therapy involved a combination of a Checkpoint Inhibitor called pembrolizumab (Keytruda) with an experimental Anti-P53 vaccine (p53MVA). The patient had extensive skin metastasis, which she endured for over 5 years and covered half of her body. After 6 weeks of this treatment, her skin mets disappeared. Imaging of her bone mets reveal improvement as well. She did this immunotherapy trial: https://clinicaltrials.gov/ct2/show/NCT02432963
This type of response is noteworthy. Granted, compared to other breast cancer subtypes, TNBC patients tend to harbor a higher tumor mutational burden, so after immunotherapy drugs like Keytruda release the checkpoint "brakes", the immune system can see the cancer and attack. Results from other checkpoint blockade Phase 1 breast cancer trials reveal durable response rates of 10-20%.
I'm providing this info because it's an example of what is possible with immunotherapy.If you're interested in this approach, please let me know and I can provide more resources.
All the best. -
Thank you all so much for your advise and concern. I wish I could take all of you to my doctors appointments with me:) Here are some answers to your questions
1. Other than the skin mets, what other mets do you? No other ILC mets...just in breast skin and one in stomach but doctors think it is everywhere but just too small to see.
Besides ILC, what is your other cancer? I have Carcinoid that started in the small intestine and spread to liver with small tumors 4-7 in total.2. I wouldn't give up. I'd get second and third opinions.
I'm seriously looking and considering my next place.
3. Have you had any advanced genetic testing to identify your mutations? No Some options are:
I asked Iowa City about this and he didn't think it would prove anything. I felt like he didn't want to waste his time with me since I have two different types of cancers.
My history:
2006 = one small 1 cm tumor in left breast, lumpectomy, SNB, 34 radiation treatments and Tamoxifen for five years, oncotypedx of 9, ER+, PR-, HER-
2011 = three more small ILC, ER+, PR-, HER- tumors in left breast and on skin. Chemo for 4 months, double mastectomy, reconstruction with LAT flap and five years of Arimidex (pathology on breasts showed that ILC was still on left side even after chemo)
2015 = one small tumor in liver found to be Carcinoid (Neuroendocrine), stomach surgery to find primary and ablation of two very small tumors in liver. Sandostatin injections every 28 days
2016 = Small tumor on outside skin on right breast and three small bumps in LAT flap. All came back positive for ILC, ER+, PR-, HER-, switched to Aromasin in late October, 2016 Surgery on December 21st, 2016 for removal of both implants, LAT flap and all skin on left side. Had skin graft from Left thigh to cover where flap was.
That's my history and I don't want to give up at all. If it wasn't for all of the surgeries and treatments, I feel good. Never smoked, quit having social drinks five years ago and weight is always average to thin. Sorry if I gave too much information but I know a lot of you are highly educated and may have additional information for me to follow up on. You guys keep me positive and searching for answers.
Thank you,
Nancy
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Nancy - The Paloma-2 Trial showed a significant increase in progression free survival in women with ER+/Her2- BC who were treated with Femera and Ibrance even when they had been previously treated with a different AI. Have you visited the Ibrance Thread? Has your local MO discussed this treatment with you? It might allow you to continue your monthly Sandostatin injections. Sending you positive vibes...
https://community.breastcancer.org/forum/8/topics/828848?page=199#idx_5959
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Nancy - my guess is the fact that you have two separate primary cancers at the same time (synchronous) is what has the doctor limiting your treatment options. But what about treatments that are used in both breast cancer and carcinoid tumors? From carcinoid.com:
- Systemic chemotherapy (including 5FU, streptozocin, adriamycin, cisplatin, DTIC, VP16-etopocide and other drugs currently under trial.
For sure, adriamycin and cisplatin are sometimes used for breast cancer. They are pretty harsh chemos though so maybe not appropriate in your case. Have you seen a carcinoid specialist? Carcinoids are much rarer than even ILC so maybe if you find someone who really knows the former and can subsequently treat the latter? I'm rooting for you -
Nancy, I'm just following up on lekker's comments with a link to the Carcinoid Cancer Foundation.
You've probably been there, but through them could you find a community that advocates for best practice, and perhaps doctors who are more versed in ILC and carcinoid patients?
I sometimes think we should be allowed to institute a public list of shame for doctors who speak to patients as the specialist at Iowa U Hospital spoke to you. It was unconscionable.
I live in Italy and had a similar encounter with THE ILC specialist, the name from Italy you see on all publications, the most famous of all the ILC MOs in Europe as far as I know, and it was €300 very badly spent. Frustrating and sad to know we can't "warn" others.
So glad you're actively looking for another solution; I'm confident you'll find it! Gentle hugs
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Nancy, I don't have much to add except to share other's concerns about your Iowa consult. It doesn't "jibe" with what I've read about ILC. You may have some single file ILC cells in other areas, but do any scans support the conclusion that you have it all over?
Sounds like they've identified your additional cancers. And offering standard treatment. I'm wondering why you haven't been offered Femara; it's often the most effective AI with ILC and with Faslodex combined. Endocrine (estrogen) resistance may be an issue too -- requiring a completely different approach to treatment.
Have you had any immune system testing like an ANA or Elisa panel? Cancer is a dysfunction of our body's immune system. With 2 kinds of Cancer it merits checking. And I believe with immunotheray is how we'll beat cancer someday.
That's as far as I'll play dr .... but if in your shoes I'd go to Univ of Pittsburg. They're #1 for Lobular cancer & where I'm going if cancer rears it's head again.
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My knowledge is limited about the current options for your cancers, so I won't suggest anything. I hope you can find the doctors with the compassion and knowledge you require. I'll be checking back. Hugs and more hugs, G.
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