HDR brachytherapy report
For those considering high dose rate brachytherapy, here is my
experience so far, 2 days after the procedure.
My prostate region is tender. It hurts when I sit or when I cough,
but the pain is not bad. I rated it a 2 on a scale of 10 (let's say a
10 is getting your finger caught in a car door slam.) In my case
I had some kind of prostatitis going into the procedure and already
had some pain. The procedure has added to it, but it hasn't been
a problem. I am able to walk and sit, but I take things easy and
go slowly and carefully sitting down, getting up, getting into a car,
etc.
I also had a prostate biopsy taken while I was under the anaesthesia.
That's not part of my treatment - it's part of another clinical trial
I signed up for to enable the scientists to get pre and post radiation
tissue to examine. The biopsy is probably contributing a bit to
the pain.
I'm actually enrolled in four clinical trials. One is for treatment and
the other 3 just let the doctors draw extra tissue, blood and urine
for scientific research. I figure I've got some tissue, blood and
urine to spare and I might as well put it to some use.
So far, urinary effects have been slight. I had a Foley catheter
for the procedure but it came out 2 hours later. I was able to
urinate right from the beginning and I did not experience significant
incontinence (a few drops with the air puffs - see below)
There is still blood in my urine, but not much. I have had a few
small clots come out. I didn't really see them but believe they were
there because I saw red trails in the toilet water. I also had some
air in my bladder, apparently caused by introducing the catheter.
This has been coming out in little puffs, bringing a few drops with
it - which is the only incontinence I've had. I have experienced
a little more urgency in urination and it somehow feels a little
different, but I don't know how to describe the difference.
My bowel functions have not been affected at all.
For me, the biggest short term problems were headache and
some nausea from the anaesthesia - lasting about 48 hours,
and a bad reaction to Flowmax. Your mileage may vary on that.
Long term - we'll see. The doctor said she was able to avoid
any damage to the urethra or the rectum. But there are a bunch
of holes in my perieneum and some (hopefully) heavy duty
radiation burns in the prostate. I'm sure it will take a while to heal.
I can't say anything yet about erectile effects. I'll find out about
that a few months from now when everything is done and the
Lupron wears off.
I haven't experienced any other treatments. Compared to
pure EBRT, this is clearly more invasive and involves more
short term surgical side effects. Compared to prostatectomy
I presume that it is less invasive with fewer short term side
effects.
Of course the real issue for all of us is first, did we get a cure
and second, how much have we given up to get it.
Time will tell.
I hope this information is of some use.
Alan
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