Breast cancer/ ProSigna results

Hi, just to let you know, I had my hospital appointment today with the consultant.

When they removed my lump, they found s ome ore cancerous cells, however this has been removed and I've got clear margins on my breat and lymph nodes.

I'm definitely having hormone tablets for 10 years and Radiotherapy. However, some patients benefit from chemotherapy and some patients don't. I'm one of those patients where they are unsure. So now I have to wait another 3-4 weeks for another appointment to see the Oncologist who will tell me what percentage the chemotherapy will be beneficial for me. They will also confirm how long I need Radiotherapy for.
If the percentage of chemotherapy being beneficial is 2% for example, I need to decide if I want it. Some patients decide they don't because it's going through all that pain for 2% whereas some patients say 2% is 2%. The test is called a pro signa test
So It's a waiting game to find out what percentage it is for me then I need to make decision. If I do end up having chemo, it be for 6 months  ‍.

I am also going to be referred for the genes testing to see if it hereditary x

Has anyone had the experience where they needed the prosigna test because it's was not clear if chemotherapy was required?

Parents
  • Hi Anjaya,

    Just came across your post. Wondered how you got on with the prosigna test? I'm currently waiting for my results, i'm 43, so pre menopausal, had one lymph node with cancer. ER8PR8 HER2 Negative...I fit into that strange grey area where they're not sure how much i'll benefit from chemo but i'm worried there's not enough evidence on the prosigna test with pre menopausal women! Just wondered how you were getting on what your score was and what you ended up doing with regards to Chemo. Part of me wants to avoid chemo and the other part wants to throw everything at this and go buckles and braces! the waiting is so hard. Hope you're doing ok! x

  • Hi, I had my results on Friday and unfortunately I scored 64 which is classed as a high risk of reoccurrence if I didn't have chemotherapy. 

    I'm now going to have 6 rounds of chemotherapy every three weeks.  I have to gave blood tests two days before each one. 

    My 1st chemo is on the 21st March and I have an appointment at the hospital on the 12th match to go through everything with me. The nurse has referred me to the wig specialist and I should hear from them this week.

    I was adamant I wouldn't have chemotherapy. I was keep saying to myself that I would refuse it but when I saw the Oncologist,  he gave me percentages of this and that and if I refuse and it comes back, then it will be stage 4 cancer and not curable. The stats he gave me was the minimum so the risk could in fact be aloy higher.

    Based on this, I'm having chemo followed by 9 sessions of radiotherapy followed by hormone tablets xx

    The wait is hard. They will give you all the stats, percentages etc if you do require it. The ProSigna test is very accurate.  I'm pre menstrual too. 

    I've been crying since Friday and still trying to take it all in. They wanted me to start next week but I told them I want my wig first x

    My lymph nodes were clear and stage 2.

    How long have you been waiting and have you had an appointment come through?xx

    Big hugs to you xx

  • Oh Anjala, i'm so sorry you've had to go through all of this and so sorry to hear you've been so upset. 

    Try and look at the positives, that chemo is really going to help you and help reduce the risk of this coming back. It's going to be a good thing and will stop this horrid disease returningk. You will get through the chemo...take one day at a time and you'll be absolutely fine...and it will all be totally worth it. You have so many treatment options, chemo, radio and hormone that it's all going to be doing its job to stop it coming back...and we have to look at ourselves as the lucky ones that we do have options and treatments available. You'll be ok. I'm sure you have lots of friends and family to lean on...and please do lean on them and make sure you look after yourself. Your mental well being is just as important as your physical health..be kind to yourself.

    I am stage 2, one lymph node involvement. Really hoping to get my results back this week...no appt or phonecall yet hoping by Friday i'll have a plan in place. It's the waiting which is hard, i kind of just want to know what treatment i'm going to be having...but hopefuly not too much longer....

    I'm here if you need to offload or chat....please don't be sad. It's a positive that they can offer you this treatment and that you will benefit from it. Good luck and hope you're out the other side of chemo before you know it.

    big hugs back x

  • Thank you for your kind words.

    You're right, we are lucky that we have all these options and only stage two cancer.

    Long term, it will help reduce the risk of it returning abd this time next year it be all over xx

    Same to you, if you ever want to talk please let me know.

    If you haven't had the appointment within 3 weeks,  I'd chase this up with your breast care nurse as it shouldn't take longer than three weeks.  I had to chase mine up. Turns out the secretary forgot to send me my appointment xx

  • Exactly - and yes here's to next year!! Good luck with all the treament I hope the side effects are minimal and you sail through. One day at a time! You've got this!

    All the best, take care xx

  • Thank you so much ️.  Hope it all goes well for you too. Let me know how you get on with your results xx

  • Hi, I hope you're ok. Have you heard back regarding your test?xx

  • Ah thanks for checking in!

    Yes i got mine back on Thursday and it was 62!!...so i am now staring down the barrel of 6 rounds of chemo like you!! Do you know which drugs you are having? My oncologist mentioned 3 rounds of EC followed by 3 rounds of Docetaxel.....I'm seeing my oncologist today so hopefully i'll find out more about start dates etc....weirdly feel ok knowing that i can now throw everything at it to hopefully prevent this thing from coming back! Obvioulsy i didn't quite want the score to be as high as it was, it's also Luminal B...so not great but i know that there are treatment options and i know with chemo, radio and hormone therapy available i'm giving myself the best chance!...it's just going to be a tough ride for the next little while but trying to stay positive as i think that can help so much in terms of recovery etc....Just can't believe i'm chatting to friends about wigs and things...all seems a bit surreal!,,and it's weird not quite knowing what side effects I will and won't get?? 

    How are you feeling about everything? I"m here for a chat whenever you need to offload. I think you said you had an appt next week and then start chemo on the 21st is that right??

    hope you're ok...

    xx

  • I'm so sorry to hear this. My score was 64 and I'm having exactly the same treatment as you.

    I have been told by the Oncologist that if my side effects are severe, the dosage can be lowered. But time will tell.

    I had my wig on Tuesday last week. I am going to give the cold cap a go in the hope that I retain at least some of my hair.

    Will you do the cold cap?

    Yes, I'm seeing the nurse on the 12th match so will ask more questions then. As you're treatment is exactly the same aa mine, I'm happy to ask any questions you may want to know and I can relay them back. 21st march is my 2st chemo xx

    I hope it all goes well today and here anytime xx 

    Wgat we need to think is this: it's to make sure the cancer does not come back at all. So it will definitely help in this xx

  • Really hope we can both manage to swerve the more severe side effects. I have two friends who had EC and they both had totally different experiences...one breezed through it and the other friend was really sick...so really hoping i can avoid the nausea!!! But i guess time will tell but they have lots of anti sickness drugs etc so guess we have to take one day at a time!!..and we'll get through it and it will all be a little blip in our life story!

    I'm thinking about doing the cold cap..but then keep changing my mind but i guess it can't hurt to try it once. I've got really fine hair as it is, i'm not sure it stands a chance!!!! I might go and get it all cut short into a pixie cut first...but again not really sure! Feels so strange to be talking about wigs and things...really hope my kids aren't going to be totally freaked out by it..they seem to be taking in their stride now but you never really know...

    Will report back after my appt today. Really hope the first round goes ok, let me know how you're getting on and any tricks or tips you pick up along the way as i'll be  there right behind you!!

    Hope appt on 12th goes ok..

    xx

  • Thank you, I will definitely let you know.

    Yes, I hope we don't get severe sickness from this. Did the hospital provide the anti sickness tablets for your friends? Are they feeling OK now?xx

    I'm the same, keep changing my mind about cutting my hair etc. I've heard the cold cap is painful fir 20 minutes then you just get used to it but I will let you know. 

    I hope my daughter doesn't get freaked out either. So far, she's been ok but time will tell xx

    Yes, please let me know how you get on. My Oncologist was better than my consultant.  He didn't rush me at all. The nurse was fabulous too xx

  • Hi, how did you get om? I hope you're ok xx big hugs xx

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