PSA 8.6, MRI PIRADS 5, Biopsy scheduled, so a bit worried
Just came across this group.
I am a 52 year old man. Routine PSA test showed an 8.6. Immediately referred to Urologist then MRI/PIRADS 5 for targeted biopsy. Biopsy still 4 weeks away so 4 weeks to worry, speculate, and research is probably not good. Every ache, pain, and moment of fatigue/weakness I've had the last several months/years has me convinced it's related to this. I understand I should not jump to any conclusions until after biopsy but just curious.
Other than the normal symptoms associated with prostate cancer, wondering if any experienced other symptoms?
I've always had back pain (golfer) so assumed it was related to that.
The last several months I've felt weak. Occasional pain during urination and more frequent trips to bathroom at night.
Occasional pains in abdomen and bruised feeling at times in different areas of my body where there in no bruise.
Just curious what input/advice others might have as I wait for my biopsy and diagnosis/prognosis.
No evidence of spreading at least from what I can understand from the MRI.
Thanks all.
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Regarding the MRI: I had two over the last eight years and both were clean. My urologist told me that the MRI only can detect on 80% of the prostate. I’ve also had two biopsies over the last 8 years. The first one was clean. I had one in August and it showed cancer in two of 14 cores. My Gleason score was 3+4=7. I decided to have it removed, which took place in November. Surgery went well and I had NO side effects! My pathology showed my Gleason was 4+5=9, and was very close to the capsule. 2 weeks ago I had my first PSA test come back at < 0.01. I’m hoping that continues. The bottom line, IMO, is leave no stone unturned until you feel completely confident about your condition and what treatment steps to take. It will help give you some peace of mind. Best wishes!
Hello, I would definitely recommend having a biopsy. It tells the story! My PSA was 4.2; however, 6 out of 12 tissue samples confirmed cancer: 3+4s.
Yes, the biopsy was uncomfortable; it was over in 15 minutes. There are some risks related to this; but, I looked at the bigger picture.
Good luck as you proceed.
Sounds like you have a plan. That is a slow rise to your PSA which is a good sign IMO. Good luck to you. I plan to be here in a year, God willing!
PSMA Pet scan is probably the most accurate. Biopsy is the best as long as you find the tumor. That may not be as simple, particularly if you MRI cannot find anything.
Dont mind me. I am just another layman trying to make some sense of the whole thing.
A urologist I met some time ago told me that in the pre-MRI era almost all biopsies were negative. In fact, doing a biopsy of a prostate with a clean MRI means sampling at random!. If there is a small cancer, finding it will just be a matter of luck. If only cancer-free areas are sampled, the result will be a clean biopsy, even if cancer is present. So in that case not even a biopsy could give us an answer that we can trust 100%. And this is another reason why I have so far given up on doing the biopsy.
Yesterday I contacted my urologist. He told me that it is possible to do the biopsy under anesthesia, but he asked me to do a new MRI first. I will do it. I therefore have to contact the radiologist and in doing so I will take the opportunity to ask him if a PSMA PET scan could be right for me.
Thanks to every body and good luck.
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With Pirad 5 your scan would show the tumor. You should have targetted biopsy.
dear wellnes100, my PIRAD is 2.
(I am not the author of this post; I joined the discussion in replay to retireddoc.
that's probably why you confuse my MRI PIRAD 2, with Greg52's PIRAD 5)
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Ooops. Sorry. You are right. You would not need biopsy for PIRAD2. There are awful stories where men went through more than one biopsy and not find anything. PSMA PET scan would be more beneficial, if only to be sure.
As for Greg52, there seems to be no reason for him to wait 4 weeks for biopsy. All the uncertainty is not necessary. He should get going right away.
Dont mind me. I am just another layman trying to make some sense of the whole thing.
This week I will meet my urologist and I will ask him if PSMA PET would clarify better in a situation like mine. However, I read that PSMA PET only comes AFTER a radical prostatectomy. But I don't understand why. Maybe retireddoc can explain it to us
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Partly because it is very expensive, and you have to wait at least a wait for the injection. Partly in the early days, doctors did not realise its full potential. As Doctor Schulz explains, before PSMA PET scan doctors may suspect metastasis. With PSMA Pet, they are 90% certain one way or the other. That makes a lot of difference to the treatment. So some doctors may consider replacing MRI.