Is it rare for TNBC to return after 5 years?
I am still in fear of recurrence. Is there lots of women here on the forum who have had their tnbc recur after 5 years?
Comments
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I am not tnbc, but I am her2+ ER/pr - . It is very rare for it to come back after 5 years, but does it? Yes. I was told I had a 1 % chance of my cancer coming back after 5 years. It was great odds, but I guess someone has to be that 1%.
Your risk is similar. It will always be there, but it is very slim. If your fear is so great that it is interfering with living your life, I would encourage you to talk to a professional.
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TNBR decreases dramatically for recurrence after 5 years, more so than hormone + B.C. that decrease gradually. The Her2+ is a bit more aggressive and problematic. That 1% chance seems a bit low for this type of cancer, but crikey! I was supposed to only have a 5% chance of a second breast cancer and I won that lottery too. Stats are just that, stats. Got to live each day as itself, no matter who you are or what you have ailing you. Keep well ladies!
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People say it's rare to reoccur after 5 years, but I've found that is not true. I was just reading about quite a few women who have had recurrences even after 15 years. I just found out that a woman I use to work with years ago passed away in 2011 after her breast cancer returned. I am just feeling down and very afraid. I hate that I have to go through life this way.
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LenaT,Don't worry, we spend too much time worrying about things that might happen, and most of the time they never do happen.
Relax tell yourself you are ok and your immune system is going to take care of you. I am almost 3 years out and I keep waiting to hear better statistics and hopefully new immune therapy and target treatments. In my heart, I feel that if my immune system could be trained, it would be fight off developing BC cancer cells.
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Thanks Meow13 for the advice.
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I went to the Dr today and was told I have tnbc - going to start my chemo this week or next - will find out for sure tomorrow. Also getting the PET and an MRI.... Any words of encouragement.... need them badly
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feelingover.....
Come on over to the "Calling All TNS" forum. You will be greatly taken care of, advised and comforted over there. This is the most difficult part of your journey - the beginning of realization that you have been diagnosed with BC, then the realization that you have been diagnosed with TN BC. I too walked in your shoes and know the horrid feelings your are dealing with - hang in there and know that this too shall pass. I am five and a half years out and never thought I'd make it at the onset, and here I am. Grateful for everyday I have had, and still pray for still a lot more to come. I wish you all the best,
Linda
Edited to add: The Calling All TNs is on the Tripel Negative forum - please make sure you introduce yourself over there.
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Feeling over Go one week at a time or it will overwhelm you . I liked books Chemo Secrets to thriving and Silver Linings . Chemo secrets will help you prepare for chemo . I am nearing the end of chemo. Have done mastectemy and than start radation in September .. Research as you are able . Pet and MRI baseline and can have false negatives(FYI) but scary to wait. Get things done before chemo .. it will tire you out . Positive thoughts your way
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feelingoverwhelmed - I second what Linda said. The "Calling all TNS" is a great thread on this forum and we all support each other. I'm am approaching 4 years out from a very large tumor and positive nodes. I'm doing absolutely great. Having said that, the beginning is the hardest part of the journey. We're here for you!
Kathy
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The beginning part is the worst. One day I woke up and cancer was not the first thing on my mind now it is on the very back burner.
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Lena,
All my docs said it is rare for TNBC to recur after five years. Hope to see you on the Calling All TNs thread. I am almost two years out fron diagnosis, a little more than a year after finishing treatment. Best wishes to you.
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Sorry you are having to go through this @ feelingover
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Thank you Placid44
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