Hello,
new member here! 2 weeks post op following ‘quadrectomy’ and ‘LICAP flap’ !! Suffering with hives… but I hear from here that is not uncommon.
my post surgery results show cancer in a LN but others are clear, ER positive, HER negative, apparently good. I’m yet to see the oncologist but Breast team tell me the MDT were split as to whether it needed chemo or not… decisions to make… I’m sure oncology will help guide me through but seems crazy to make a decision myself on this. Number 1 priority is to reduce risk of recurrence/secondary cancer… I don’t want to regret not doing all I can now to prevent that.
Any advice from others being in a similar situation?
Hi SunMey
I was diagnosed with triple negative breast cancer in April 2022 and 1 of 2 sentinel lymph nodes removed was found to have micro deposits of cancer cells. The lumpectomy was successful with clear margins.
When I saw my oncologist he said that, like you, I was borderline for chemotherapy. He told me that some oncologists would count the micro deposit as 'clear' so not offer chemotherapy, but he was happy to approve chemotherapy if I wanted to have it.
I decided to go ahead as I didn't want to wonder if I was to ever get a recurrence, would I have not got the recurrence if I'd had chemotherapy.
All the best with whatever you decide to do
Thank you for your reply.
This is exactly where I am right now. Not seen the oncologist yet but feel I want to be as aggressive as I can with treatment now. That way, if I do get recurrence in the future, I’ll at least know I did all I could to prevent it while fit and well in my 40s.
Seems quite daunting for it to be a choice… I’m hopeful my oncologist will guide me through when we meet next week. Tho feel they’ll need to be pretty convincing to satisfy me that i don’t need it!
I expect everyone’s situation is different but would be interested to know how long your chemotherapy was for? if you feel happy to share.
many thanks,
Hi SunMey
I had two different types of chemotherapy. The first was epirubicin and cyclophospamide, or EC for short, which I had every three weeks for 3 cycles. Fortunately, I got off fairly lightly with main side effects being hair loss and a sore vein. For the first 10 days I felt just a bit under the weather and slightly tired but for the rest of the 3 weeks I felt completely fine. So that was over 9 weeks.
Then I had 12 cycles of paclitaxel, which was given weekly. This was kinder than the previous chemo and I just felt a bit tired for the first evening.
So in total my chemo lasted 21 weeks.
If you have any other questions I'm happy to answer them.
Anne
Hi I’m having the same treatment as you
woukd it be ok if I dm you
Hi SunMey
Have you since seen the Oncologist?
I'm similar - post op, ER+, HER2-, micromestasis in sentinel node, borderline chemo
Hope you've had some progress
Cujo4498
Hi,
sorry for delay!
in the end, oncology was quite black and white about it all… very clear that they would recommend chemo.
Just had the second cycle of treatment today. So far all much like Anne - from earlier in this thread.
I went to the Oncology appointment with the mind set that unless they were gong to tell me i didn’t need it - then I was going to go for it (if came to a choice).
‘Macroscopic LN deposits’ in 1 or 3 biopsies, and some more nuances in the microscopic findings of the tour to do with vascular and nerve involvement tipped the balance for oncology.
There was a bit of chat about a trial for genomics test to guide therapy options- similar to one which is offered in post menopausal women (which I believe is there tumour tissue is sent or US for tests) - but my understanding this is not currently offered for premenopausal as part of standard therapy- it is in trial, and my centre had just closed to new recruits for that one. This was a blessing, because in the end, and with discussions with family etc. I felt I didn’t want to know if I was ‘high or low risk’ and that I just wanted to go ahead and have everything on offer now to ensure the risk of recurrence is as low as possible. So, should that happen in the future I can be satisfied I did all I can when younger and (ahem) fitter! And then I can bury my head in the sand!
not a nice undertaking- but in a years time it will have just been a few months of treatments and side-effects of manage which will hopefully be a faded memory!
I know that currently lots of us will have chemotherapy when perhaps we didn’t need it… but for me the assurance around whether to veer from the ‘standard treatment’ wasn’t there.
Promise to keep my eye out on this if you need anything. XL
You should have been offered an oncotype dx test. That is for pre and post menopause.
I completely understand the not wanting to know if high or low risk though.
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2025 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007