Phesgo Success

Hi I'd just like to come on here to offer some hope and share my story.  I was diagnosed with Her2 and ER stage 3 breast cancer in 2013.  Given Fec T chemo, radiotherapy and mastectomy.  I had herceptin tablet for a year and 7 years of tamoxifen and 2 of letrizole.  Last year I was shocked to be diagnosed with stage 4 metastatic breast cancer in lymph's, lungs, liver and bones.  The diagnosis stated it was 'bulky' and they would try and extend my life.  Well I wasn't having that! I've had 7 rounds of doxetaxil with Phesgo and now have Phesgo injection every 3 weeks along with a bone infusion every 3 months.  Chemo ended July 22 and once I started to recover I have never felt better.  My oncologist told me at the beginning you are going to be ok because of your mindset and she also said Phesgo has blown medical science and to have faith.  At my recent scan she told me 14 months after diagnosis there is no sign of cancer and I am in full remission!!! I cannot believe it.  I just want to share this with anyone who is feeling there might not be hope, there is, there are new treatments coming out every week I'm told and this one has been a huge success for me. Sending love and prayers to you all Cally xxx

  • Hi Cally,

    Thank you for your quick response.. that sounds very reassuring, hopefully it will be the same for me..

    Wishing you all the best too.

    Lizzy

  • Hi Lizzy, I'm on Phesgo too. I'm halfway through the 18 injections. I've had chemo and lumpectomy with lymph node clearance. My hair is growing back since finishing chemo in January. It's coming along slowly but I'm enjoying not having to style it and get it cut every few weeks! My nails are also growing at a rate of knots, which is good because EC and Docetaxel really messed them up. Yes, it does seem strange to still be having active treatment after being told we're cancer-free - I'm having five days' radio next week as well as the Phesgo, and I'll be starting bisphosphonates in due course. I just have to trust that my oncologists know what they're doing and only prescribe what will give us the best chance. Love and prayers, Amy x

  • Hi Amy,

    It's good to hear you are doing so well and reassuring for me, so thank you. I had Docetaxel too it destroys everything I think, I lost eyelashes, eyebrows etc.....

    My nails and hair are just beginning to recover slowly (albeit grey!) It makes such a difference to have some hair, feel a bit more normal.  Hence why I'm so worried I might lose it again.. like you it is quite refreshing not having to worry about your hair, it's very simple having a crop!

    I had a call yesterday and am starting the Phesgo on Weds so wish me luck.. 

    Best of luck to you too with the radiotherapy and wishing you well, it's such a hard journey, and like you say we have to trust the experts.. By the way I've never heard of bisphosphonates?

    Take care, 

    Lizzy..

  • Hi Lizzy, thanks for the kind wishes. I've coped really well with chemo and surgery, so hoping for more of the same with radiotherapy. My eyebrows don't seem to be growing back - I still only have a few hairs that didn't fall out. Hoping they will come back in time! Bisphosphonates are prescribed to strengthen the bones. In my case (early, locally advanced BC, post-menopausal), it's to prevent osteoporosis and reduce the likelihood of cancer coming back in the bones. I was also HER2 positive and started Phesgo with the last four chemo cycles (I had 3x EC and 4x Docetaxel). Did you not have it with your chemo? Best wishes, Amy x

  • Not heard of phesgo yet from my team can I ask your ages . I wonder if only younger women are offered this?

  • Hi I'm 51 so not just younger women I believe. It's particularly for HER-2 positive cancer.   Hope that helps.

    Best Wishes Cally

  • Hi Amy,

    Had the first PHESGO injection this morning, seems to be fine, left a nasty red mark and is a bit sore..

    I forgot to ask, maybe you know, are you meant to leave the area covered (plaster)

    And no I've never been told about bisphosphonates , so thank you for that, I have an appointment with my consultant in a couple of weeks so will ask her about it. 

    Good luck with your radiotherapy

    Take care

    Lizzy

  • Hi, this is great to read thanks for sharing, I am following a similar journey, first diagnosed in 2007 with stage 2 had a lumpectomy Fec Chemo, radiotherapy and tamoxifen for 5 years. Then diagnose again in 2015 another lumpectomy and radiotherapy and letrozol. In Oct 2023 I was diagnosed with metastatic breast cancer and in the lungs, liver, chest and bones.  Currently on session 5 of Docetaxel chemo and Phesgo injection and had a PET scan after 4 chemos and the scan showed significant reduction in all areas which the Oncologist is now saying he may only give me 6 chemos rather than 8 as the results are so promising so it’s great to read how well it’s going for you long may it continue ️