Going for Prostate Biopsy Tomorrow ….Looking for Opinions and Thoughts
Hello,
I am going for a prostate biopsy tomorrow which I am dreading.
Here is a little background on me. I am 64yr in good physical condition. My PSA has always been high. When I first got it tested 9 years ago it was 5.65 in the years following it was 5.4 - 5.1 - 5.79.
All DRE were fine. Have had BPH for years. Had an MRI done and showed my prostate was a giant size of 171cc. Showed several benign nodules and one PIRADS 3 lesion 1.2 cm. Really don’t have any issues other than getting up 3x a night.
From what I have read with my results the my PSA density would be low which is a good thing. Just trying to find something positive before tomorrow lol. I have read for months about the prostate and it is very complicated. Anyone had a similar experience like me.
What are the odds that the lesion and PSA is all from BPH ?
I live in Indianapolis by the way.
Thanks
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One reason I transferred my care to an NCI designated cancer center, other than I thought they would provide a higher standard of care, was I thought it likely they would do a fusion biopsy. I was also interested that they use a perineal approach as opposed to rectal. I think they only do perineal. But, it turns out, they only use fusion when they think the circumstances warrant.
My community urologist was going to do his normal "cognitive" biopsy, i.e. he looks at the relevant MRI image and remembers it when he's sticking the needles in, guided during the prcedure by ultrasound.
Anyway, as a new patient with no firm diagnosis, facing a busy time in the NCI center doc's schedule, they offered me a perineal non fusion biopsy several months away.
This was going to be 3 months from when I first saw disturbing MRI results, some ten months from when I saw my first jump up in my PSA reading.
There were lots of reasons for the delay: a few months of me denying the problem, time waiting in line for a new patient appointment with a community urologist who then retired and shut his practice down, time to wait for a new patient appointment with the next community urologist, time to wait for the appointment with the NCI designated cancer center urologist new patient appointment, etc.
I was quite uncomfortable about any further delay. So, I went back to my latest community urologist. His schedule had me getting a biopsy a week later. He then ordered a PET scan. That took place quickly as well. I was glad he had time to do this.
Perhaps the fusion guided biopsy would have been better. But I now had a biopsy result and a PET scan result to show the NCI designated center. Suddenly, I was given an appointment a week later. They decided to redo the "outside" pathologists report on the community doc's biopsy, but they didn't order a new biopsy. They are ordering treatment. I take it they didn't think they'd get relevant info from a new biopsy.
I was glad I took the opportunity to have a biopsy done sooner rather than possibly better and later. I have respect for the community urologist who did it. He had said the MRI had shown a lesion big enough he could not miss it. He found cancer in all the places indicated by the MRI. He did a perineal biopsy at my request even though his usual and faster method is rectal.
I don't regret transferring to the NCI designated cancer center either.
Obviously, your mileage may vary.
@climateguy
Hello,
Do you remember how big your lesion was ?
My is supposedly 1.2cm.
I don’t know for sure what it considered large …over 1.5cm ?
@dgd1953
You are happy with your urologist and that is what is important. It is your urologist and you who make the decision of what is best for you based on your urologist who has your full medical history and has examined you.
It appears you have a very experienced urologist who wanted to do biopsies to rule out and found your PC. Appears to me you are in good hands and in today's world when you feel that way does wonders with your journey through PC.
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Where are you having your biopsies? Are you at a instiution with experienced urologists.
A MRI/Fusion is a very accurate and widely used way to do biopsies. I say that because that is what I had at Mayo Jacksonville. I did have to asked my urologist what it meant MRI/Fusion biopsies.
What it means is the urologist doing the biopsies is using the MRI taken to guide them to suspicous areas. Do you have access to call or portal message to your urologist seeing you about your cocern with having someone else do your biopsies?
I think that would help reduce your anxiety over a different urologist doing procedure. I make this post as that would have been what I would have done if this had happened to me and a differernt urologist was going to do my biopsies that was not the one I have been seeing.
If you are at a large and experiencd medical institutions probably have a wide selection of expereienced urologist but always good to reach out with your concerns to your treating urologist.
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One of my lesions was 3.8 x 1.2 x 1.8 cm. Compared to the size of the prostate gland, possibly colossal.
The docs don't mention this as particularly dangerous, they call my case high risk due to the fact that cancer was found outside the prostate, i.e. in the seminal vesicles.
@climateguy the three big questions are:
1) what is your Gleason score?
2) is there a Cribriform pattern to the cancer?
3) have cancer cells escaped the prostate gland?
Answers to these plus considerations about you, your medical status any any other challenges, drive your individualized treatment options a decisions. You want o be comfortable with the doc(s) who present your options, and their thoughts about which might be best for You.
My Urologist referred me to a wonderful Medical Oncologist to discuss further. It's good to have multiple docs.
@steveduke
While cribriform can be a serious if it is large cribriform these other prostate issues are just as aggressive.
Intraductal, Seminal vesicle invasion, EPE or ECE. (Extraprostatic extensions extra capsular extensions)
@rider51
Thank you for your reply…I appreciate it.
@jc76
Yes, I am going to a big Urologist group here in Indianapolis. I hear to go to a “ Center of Excellence “, but I’m not sure if where I am going is considered a center of excellence. How do you find a center of excellence ?
Thanks
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I am not sure who was originator of the term Center of Excellence. It seems subjective to me because no one knows all the great medical institutions that are out there.
There are very big medical centers in every state that have excellent medical diagnosis and treatments. I think the bottom line is that you are being treated by experienced and knowledgeable medical doctors and the institution has the latest diagnosis and treatment equipment and program.
I ended up at UFHPTI and never appears on posters center of excellence list. However it has been treating PC since 2006 with proton radiation. It is one of the most experienced medical institution treating cancers with proton radiation.
Every single state has send or self referral patients to UFHPTI including Mayo Jacksonville as they don't have proton radiation at Mayo Jacksonville (yet new cancer center with proton coming). I believe the number of other countries with patients coming there is well over hundreds. They are very large and have 5 gantries that were recently updated to latest proton radiation equipment. The federal government just chose UFHPTI to receive a 25 million dollar grant to study long term proton and photon radiation treatments.
You will see names like Mayo, Cleveland Clinic, John Hopkins but there are many many more that have excellent medical programs and treatments.
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