My right kidney was removed 9 weeks ago. It was grade 2 with intermediate risk. A 25% risk of reoccurring within 5 years. Have been offered Pembo immunotherapy starting on 18th Dec. It will be every 6 weeks treatment lasting 1 year.
I am wondering is there anyone out there who has been on Pembo and how is it working out for them.
many thanks,
Sandysea
Hi Artful
Oncology review at Charing Cross tomorrow - routine I guess - and 2nd jab on Monday. May have been lucky so far re side effects so keeping my fingers crossed for Monday that no others start to show.
Are you not having infusions then Michael just jabs not heard of that . Good luck all the best
Sorry - it's an infusion - I call it a jab! It's a bag of the drug that gets pumped in over c30 minutes.
hiya sorry to but in been meaning to but things change so quick with cancer and treatment i have just had my second infusion of immunotherapy at sheffield western park lovely people i have had very little side effects as i am still contending with the side effects from my radiotherapy on the spine and pelvis been on this journey 2 and half years now the cancer has travelled to my lung hence the pembro as i call it i didnt put much on profile its been such an up and down road hope to chat soon if theres any change thanks bob
Hi Phil
I didnt have any symptoms, I had a scan for another reason and they saw the tumour on the kidney. I was quite lucky really that they caught it. It was grade 4 aggressive though so even though it was removed Ive been on the pembro since. Have to say the staff at the City hospital are brilliant though, they are in regular contact and whilst there is always the worry of it coming back I try not to think about it and stay positive. What are your next steps?
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