Anyone with experience of Brachytherapy for Oesophageal cancer

My first post! I was diagnosed Stage 4 G3 SCC Oesophagus / T4 N1 M1 in November 23 and underwent 4/6 rounds of Capecitabine/cisplatin with good results, partial shrinkage of tumour and evidences for lungs. CT scans every 3 months so slight increase in size of tumour in November 24 so had 5 radiotherapy sessions. All this time my swallowing problem had nearly disappeared but now come back over this winter. Had meeting with oncologist yesterday and have ruled out more chemo for now and also immunotherapy due to some lung scaring.
I have now signed up for Brachytherapy as option as do not want to just do nothing. I realise that may be more scarring and affect my eating forever so has anyone been through this had how did it affect them? I am actually very concerned about becoming more fatigued and how long it may last.
  • Hi Rosiecat10,

    Welcome to Cancer Chat. It's good to hear you've been getting on OK with treatment so far.

    You mention starting brachytherapy as a treatment - do be sure to discuss any questions or concerns you have with your doctor or medical team as they will be best placed to advise.

    We also have nurses available if you'd like to talk things through at all. You can reach them on freephone 0808 800 4040 - Monday-Friday, 9-5.

    If others on the forum have similar experience to share then hopefully they'll see your post and send a reply. From the homepage of the forum you can also use the search bar to find other discussions and people to connect with.

    We're always here if you need it and I hope the forum can be useful for you.

    Wishing you all the best,

    Ben
    Cancer Chat Moderator