Hi, I am new here. I was recently diagnosed with PC following my Dad's diagnosis.
I am 54. My PSA was 4.97, MRI & Biopsy revealed Gleason 7 (3+4) contained. I have been given 4 treatment options. AM, which I don't want to consider as fell I would be doing nothing while it potentially gets worse. Surgery, for which the potential side effects worry me, plus being out of action for so long when Dad is not well (He has stage 4 that has spread widely). Radiotherapy, which is 5 courses of Stereotactic Radiotherapy over 2 weeks or Brachytherapy. I was told all are 95% effective, so I've been told it's all down to my choice.
Does anyone have experience of Stereotactic Radiotherapy or Brachytherapy who could help me with my decision. I would appreciate peoples experiences and thoughts on this.
Many thanks.
Hi Drewpup
SR 5 sessions is relatively new but have read good things about it, there are people on here who have had it, hopefully they will appear.
Brachy also read good things about, in my mind SR seems dead easy as only 5 sessions but just my opinion.
I had 20 sessions of Radiotherapy and was very happy with that many years ago.
See what others say
Best wishes
Steve
My mum had stereotactic radiotherapy at Tonbridge Wells (Kent) 4-5 years ago and was treated to a fabulously accurate treatment for her lung tumour.
It’s got to be the way forward due to less “body” being affected by the rays, as it’s more focused on what it’s aimed at.
It’s the same principle as radiotherapy, a tatoo, a few days of treatment and a wait for scans for results. Simples.
Good luck with what you choose
Hi Drewpup no experience of surgery, but if I were given the same 4 options I would go for SABR or Brachytherapy. I had SABR 3x13gy Feb 25 and think it has worked. Our expert on Brachytherapy is Alpine Wanderer so have a look at his profile.
Best wishes, David
Please remember that I am not medically trained and the above are my personal views.
Hi, I had LDR Brachytherapy and nothing else a year ago.. You may wish to look at my profile.
Thanks for that, good to see your experience as you had a very similar diagnosis to mine. I have a consultation with the Bracky people just after Easter, so will be able to base my questions to them on your story.
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