Hi. I'm new to the group, and so glad to be here. Two months ago I was diagnosed with bladder cancer. I had a biopsy on the tumour they cut out, the results came back as a grade 3 tumour on the inside of the lining. Then I had another biopsy done, this time from the muscle surrounding the bladder, to see whether the cancer had invaded the muscle. The result was both good and bad news: the cancer had not (they believe) invaded the muscle, however they also found, and took out, a carcinoma in situ which was found in the site of the original tumour. So, both original tumour and this carcinoma were both ‘high risk’. I had that last biopsy on the 16th August. Before they begin whatever treatment is decided upon they now need to do a CT scan of my abdomen and also of my chest. This, the oncology nurses tell me is standard practice before a final decision can be made on the type of treatment I will have to prevent, hopefully, more tumours from growing. So I have what they have termed Non Invasive Bladder Cancer. The oncology nurses tell me that in their experience the treatment I will most likely have is called BSG or immunotherapy. I'm so scared. Can anyone give me any relief from my …..well, my terror, frankly, or any words you think might help? Thank you in advance, very much.
Yes Seamoth, that's right, Mitomycin after the 6 BCG and recurrence. Mitomycin is a chemotherapy drug sometimes used into the whole system for other types of cancer. So be careful if you are looking it up, to look it up with reference to bladder cancer.
The beauty of having bladder cancer if one is going to have any kind, is that the immunotherapy and chemotherapy can be given into the bladder as long as it remains non-muscle invasive. This means that there are not the same side effects. So no hair loss and most people do not have much if any nausea on these treatments. The main side effect for my husband was tiredness for the rest of the day and next day.
It also means you do not have to have constant blood tests to monitor white cells etc or take handfuls of anti-nausea pills. All worthwhile if needed, but not needed for these two treatments. Also usually you have to remain at the hospital for perhaps an hour or two on the first of a course but can go home as soon as the dose has been put in your bladder ['instilled'] for the rest of the course. Many people drive themselves to and from.
Hope this is helpful, Denby
Hi Seamoth, like you I have a stage 3 bladder cancer, but mine is muscle invasive. I have had two ops to remove the tumour and any remains. I am going for the pre-treatment appointment on Wednesday to set up the radio therapy for when my treatment begins. I am having Radio Therapy and Chemo Therapy. I also have a second problem in that I have Autoimmune Hepatitis, which is dangerous for the liver. A careful eye will be kept on my liver functions because the Chemo will be stopped if anything untoward occurs. I know the Oncology staff will do all in their power to sort the problem out. I have had a CT scan recently which showed no apparent spread of the tumour,so I am optimistic for a good outcome. I wish you well for your forthcoming treatment. As Old Bob has said, he has lived with this for a number of years. Every year the treatment gets better and your quality of life is maintained. Good luck friend.
Good afternoon Seamoth , how are you today ? . I’ve not had mitomycin but a series of BCG , I completed the 15 th last week. There is no need for panic or fear , it’s quite straight forward and takes only five minutes. It’s uncomfortable rather than painful . I’ve always driven to and from the hospital for treatment and the two hour wait afterwards to empty the bladder is not difficult.. I’m not aware of any side effects and it seems to work, best wishes, J
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