Triple Negative Breast Cancer: What treatments are you having?

Posted by thielmann1 @thielmann1, Dec 9, 2021

I have just been diagnosed with Triple Negative Breast Cancer after having Estrogen Positive Breast Cancer for 21 years. Is anyone familiar with this diagnosis and treatment that you are having for it?

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@mdr3

I am a firm believer in Zometa (let me just say that out of the gate). I had the attitude that I would do anything to increase the risk of recurrence, anytime, anywhere (and that's one of them). The major downside is the inability to receive dental care while on it (at least around here). I finished my 6th infusion 6 months ago, and will be going to a med/dental hospital for overdue oral surgery (secondary to the chemo I had in 2019). My oncologist wanted me to wait a full 6 mos. Yes, Zometa has recently been shown to have tumor suppression properties in the bone. Initially it was prescribed for bone strength.

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(I'm pretty sure you meant DEcrease, not increase...and I totally agree with your sentiment about doing anything, anywhere, anytime!) 🙂

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@lnlowe70

(I'm pretty sure you meant DEcrease, not increase...and I totally agree with your sentiment about doing anything, anywhere, anytime!) 🙂

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Hi I am on the zometa infusion, too. My question is after TNBC how often are your check ups after treatment is done. I was recently told somd are doing virtual appointments which is crazy. I want somebody checking my masectomy sight because I could miss something. My appts so far have been with the Dr.
Good luck to all.

Thank you

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Theilmann1- you asked about course of treatment. I was stage 2A with 2.4 cm tumor. I was told that if over 2cm, the treatment was chemo, then surgery. I also learned that I had the ATM gene. I wanted to avoid radiation, so I did a double mastectomy with no reconstruction. I had clear nodes and clear margins and minimal lymphovascular invasion. I was told that the removal of all the breast tissue was a positive thing for the lymphovascular invasion. I did not reconstruct because I wanted to be able to easily feel any abnormality. The worry of reoccurrence will always be with me. That said, I felt good through all the treatments, the surgery and follow up. I have read of your journey and you have been through a lot. Wishing you the very best.

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@lnlowe70

(I'm pretty sure you meant DEcrease, not increase...and I totally agree with your sentiment about doing anything, anywhere, anytime!) 🙂

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OOPS!! You're so right! I won't analyze the psych loose associations there. I wish everyone well with these decisions. Never hesitate to request a second opinion on anything!

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I have metastatic triple negative breast cancer. I am 77 yrs. old. What treatments did anyone who has this diagnosis receive? I would be grateful for any replies. bemar23

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@miles5513

I have metastatic triple negative breast cancer. I am 77 yrs. old. What treatments did anyone who has this diagnosis receive? I would be grateful for any replies. bemar23

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Hi bemar23,

I was diagnosed with stage 3B triple negative breast cancer two and a half years ago when I was 38, and had some treatments that metasastic breast cancer patients have.

Besides chemo and radiation and surgeries, the treatments I had that were specific to metastatic TNBC were a year of keytruda and a year of xeloda - the keytruda concurrent with chemo and then surgery and radiation, and xeloda I started during radiation as an oral chemo that would specifically target any cancer that was in the bloodstream.

Hope others are able to chime in too for more specifics, but if you have any questions for me I'm happy to help.

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@seathink

Hi bemar23,

I was diagnosed with stage 3B triple negative breast cancer two and a half years ago when I was 38, and had some treatments that metasastic breast cancer patients have.

Besides chemo and radiation and surgeries, the treatments I had that were specific to metastatic TNBC were a year of keytruda and a year of xeloda - the keytruda concurrent with chemo and then surgery and radiation, and xeloda I started during radiation as an oral chemo that would specifically target any cancer that was in the bloodstream.

Hope others are able to chime in too for more specifics, but if you have any questions for me I'm happy to help.

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Thank you so much for sending your diagnosis and treatments for the Stage 3 Triple Negative Breast cancer. I was in treatment this am (April 14th) with Keytruda, a 30 min. drip every 21 days. I will be having a biopsy of cancer in my liver. Will reply when I have biopsy & results. bemar5513

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@miles5513

Thank you so much for sending your diagnosis and treatments for the Stage 3 Triple Negative Breast cancer. I was in treatment this am (April 14th) with Keytruda, a 30 min. drip every 21 days. I will be having a biopsy of cancer in my liver. Will reply when I have biopsy & results. bemar5513

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Hi @miles5513, I moved your question to this existing discussion on the same topic:
- Triple Negative Breast Cancer: What treatments are you having? https://connect.mayoclinic.org/discussion/triple-negative-breast-cancer/

In addition to @seathink, you can easily connect with other members talking about triple negative breast cancer treatments, like @thielmann1 @kk57 @olg1 @dolphina3 @lnlowe70 and many more. Click the link above to read through previous posts.

How are you tolerating Keytruda so far? Or was today your first infusion?

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@kk57

Greetings @thielmann1. I’m sorry to hear about your diagnosis. I was diagnosed with triple negative breast cancer last February. I had a DCIS (Stage 0) and an invasive (Stage 1A). The not-so-good news about triple negative is that it is usually more aggressive/faster growing and usually does not respond to hormone-related therapies. While my cancers were caught early, they were also grade 3, and I had a very high Ki-67. These are both more aggressive indicators as well. For me, it just meant I didn’t want to delay moving forward with treatment.
The good news is there is no reason for me to have aromatase inhibitors post treatment, which is nice to be able to avoid those side effects.

Due to the aggressive nature of my tumors, and especially the invasive, Mayo Clinic had me in chemotherapy within two days. Thus, by the time I had surgery, there were no active cancer cells in my breast tissue or lymph nodes. I had never heard of having the chemotherapy first before surgery, but this seemed like a great approach to me. Something to consider with your medical team, if appropriate.

FYI. Other factors played into my surgical decision - unrelated to being triple negative and more related to avoiding future cancers. I have a strong family history of breast cancer. I’m 64 years old. I had a previous atypical lobular hyperplasia (ALH), a future cancer marker. While I didn’t test positive for the BRCA gene, I do have another potential genetic marker (STK-11). I also preferred to avoid radiation. Thus, I opted to have a double mastectomy with reconstruction. I am halfway through my reconstruction, and am at peace with all my decisions. They found several other small DCIS and ALH In the breast tissue they removed. I would likely have been back with another cancer had I gone with a lumpectomy, So this was the right decision for me. Everyone is different. And your decision will be the right decision for you.

So again, to me triple negative means don’t delay, and it also means hormone related therapies are not effective/necessary. Forge ahead with your medical providers. Prayers you find the best treatment for your situation. Blessings to you on this journey so many of us travel.

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I also have triple neg breast cancer and started chemo first in January. I am in my 5th cycle and will be done mid-June. Then surgery and potentially reconstruction. Can you tell me what kind of reconstruction you chose and how you decided?

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Hello everyone
I was diagnosed 3/15/2023 with Stage 1a TicNo Tnbc local reoccurrence after 5 1/2 year of being cancer free. It came back in the same area of the lumpectomy in 2017 and a 1.7 cm behind the nipple. Had a PETSCAN/CT all came back negative except in the breast. Also had a MRI with contrast. My treatment consists of Carboplatin, Abraxine and Keytruda, 4 cycles every 21 days with surgery following all treatments. I believe I will have one more cycle after surgery to clear up any remaining traces in the system. The most frightening part of this whole thing is that there is a shortage of Carboplatin everywhere! My doctor called my on 4/11 and said they may not have it for my treatment on 4/14 but name was first on the list. When I arrived for my treatment they were able to get it for me but could not guarantee they would have it for my next treatment. I am halfway through my treatments with no solution to what will happen next. This is very frustrating but I am going to remain positive! Hopes this helps
Take care.

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