Triple Negative Breast Cancer: What treatments are you having?
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?
Interested in more discussions like this? Go to the Breast Cancer Support Group.
I was diagnosed w/tnbc stage 4 on 3/22/23. It was a recurrence. The tumor has spread to my lung and chest wall and bones . I was told my doctor that I cant have surgery to remove . I also had positive breast cancer stage 3 in 2014 and went remission at the year after I had surgery, chemo, and radiation. last May, I had chemo Enhertu for 6 month then the tumors started grow again. Now I am using chemo Trodelvy for near one months now. I will find out if it
is working on my next scan test.
I was diagnosed TN in September 2021, had a double mastectomy the following month, and have not had regrets about my decision. At some point I may try some kind of minimal padded-bra type thing but so far I have not done anything like that nor felt the need. It takes a little while to adjust to the change in how my clothes fit; I was not shapely before the surgery, so most of the adaptation has just been in my own mind. I was 68 at the time of diagnosis, and I'm 71 now. I wanted to avoid multiple surgeries, and I like being able to know that everything I see and feel is actually my own body; I feel more aware of my own condition and health with nothing external in the way. The good thing about TN is avoiding so many complicated decisions and side-effects of the treatments for the positive-types of breast cancer. The negative thing is that there's a big empty space where you are on your own to stay distracted and avoid thinking of that higher chance of a return cancer in those first several years.
Frankly, I didn't want to do multiple breast surgeries of ANY kind, either multiple lumpectomies, mastectomies, or the multi-step, drawn out reconstruction processes I heard about. If my life is to be shortened by this disease--and I hope it's not--I want to spend as little of it as possible anticipating or recuperating from surgery. I'm sure you will be fine, and will be comfortable with your decision once you have settled on your own priorities going forward!!
Welcome @marywei. You may also be interested in joining this discussion:
- Has anyone been given Trodelvy?
https://connect.mayoclinic.org/discussion/has-anyone-been-given-trodelvy/
How are the side effects with Trodelvy for you?
We are close in age and diagnosis and my thought process was very similar.
I just wanted to heal and get on with it. Wishing both of us good health and sunny days.
Callalloo,
thank you for sharing this article. I have been avoiding information that I did not want to handle. Some of my avoidance was knowing some of these realities. I am a retired oncology nurse and shared this with some of my nursing friends who have been involved from day one.
All the best to you.
Robin
Interesting. All coincides with all info from oncologist and surgeon.
I could not find a Ki-67 result in my chart.
I am 45 years old recently diagnosed with TPN, the tumor is in my left breast measures 6.2 x 5.7 mm no node involvement. I am waiting for my appointment with the oncologist to see what she says about treatment options, I know everybody is different but I am wondering about treatment options for this case.
Hi @erikamilena. Sorry to hear of your diagnosis. I was diagnosed with a subtype of triple negative breast cancer on Sept 27, 2024. I had a bilateral mastectomy on October 23, 2024. I did not need chemo or radiation. I chose to have reconstruction, with tissue expanders inserted during my mastectomy surgery. I just went through surgery on March 5 to swap out tissue expanders for implants and also had fat grafting of my stomach to fill in around the breasts. Hope this info is helpful to you. Let me know if you have other questions about the process. ( I am 59. My cancer was LGASC stage 1b.)
Thanks so much for your reply, in the first appointment with my oncologist she said that only surgery could be an option for me if there is no metastasis to other areas, but I am hesitant about that, I am thinking that chemo will give me some peace of mind but I am also considering about the side effects. So far the test results are ok and I am still waiting for genetic testing.
With a 6.2 lump already… I believe you are considered a 2a or b. It wasn’t easy for me to jump into my 2a tnbc decision to have a bilateral mastectomy, but that’s exactly what I did. Hands down with saline implants at surgery… and now on dose dense chemo. None of this is fun or easy… but I want to go with the tried and true best chance to live…no matter what stage. It’s better than having to cut my legs off. Getting my decision over with felt good.
The job at hand is honest, unwavering, personal research if you are able… every step gives you new information to look up. My doctor would’ve given me targeted radiation and a lumpectomy followed by chemo… but it didn’t make sense to me when I could have 2 nice new saline boobs and get the bad stuff completely out… do chemo and try to have a few more years of quality life. Btw… taxol for my 1st 12 weeks is going well… I’ve totally changed my diet. Homemade ginger tea all day long and no benzos… yay yay yay… might not be so easy when the big dogs come in, being the ac part of an act treatment plan. I still have normal hair… but my bald headcover awaits…
Be brave… be strong… be beautiful…