Very interesting pathology report about cribiform
I found this very interesting after reading on this forum and internet about cribriform being a negative factor. I've been to 2 different centers of excellence and none of the doctors ever mentioned it on biopsy report. When I asked the chief pathologist at a center of excellence who read my slides for 2nd opinion about cribiform on a biopsy report with a Gleason score of 4+3 her reply was:
"In summary, the presence of cribriform pattern is documented in all cancers that have pattern 4 but not always stated on report"
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@surftohealth88 My second opinion at a CCC facility stated I had one pin with 10% Crib and metaphorically yawned. Gave me a 70:30 chance of never having to revisit this after my current treatment. Oncology Surgeon used it as a selling point to get the removal job which I now view as manipulation. If you haven't personally seen the slides, how can you emphatically say the doctors information is false? The value of this forum is prostate cancer patients personal stories and experiences. What did your slides look like?
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1 Reaction@chippydoo
I know exactly how my husband's slides looked like and also how his post-op slides look like since I asked to see them. I know exactly how cribriform looks like as well as EPE, capsule, nerve bundles, etc.
Actually we had one hour meeting with UCSF pathologist himself and went through slides one by one and had in depth discussion.
I am biologist and I worked with microscope and "slides" for years and I can tell you with certainty that cribriform or IDC or any other "feature" can be easily seen IF they are present and IF person who is doing examination pays attention and is not rushed to go to lunch or chat with a GF in the hallway, or is just sloppy.
I expect from myself nothing but "my best" in everything that I do and I loath sloppiness and willy-nilly untrue declarations spewed at patients.
I hope this eases you mind.
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2 Reactions@surftohealth88 I totally agree that saying all Gleason 4 slides have cribriform is false. What I just learned from you is that a grouping of Gleason 3 cells can legitimately be upgraded to Gleason 4 if there is some cribriform pattern mixed in. Additionally, Gleason 4 cells with cribriform pattern can be upgraded to Gleason 5.
What I had previously thought was that a grouping of Gleason 4 cancer cells stayed at Gleason 4 and either had cribriform pattern present or not. I had always thought of cribriform as an independent feature in the same way that intraductal stands alone. I did confirm with google AI that cribriform affects the Gleason score while intraductal stands alone and does not affect the Gleason score.
@wwsmith
Unfortunately, intraductal seems to be much more difficult to Treat than cribriform.
Here is a really great video UCSF did discussing Cribriform And intraductal. They said that they found that most of the time when somebody had intraductal they also had cribriform.
They also mentioned that somebody that was 3+4 would have a five in their Gleason score if they had cribriform. Discussed in this video.
https://www.urotoday.com/video-lectures/a-journal-club-for-patients-with-prostate-cancer/video/mediaitem/4452-unfavorable-histology-classification-aims-to-reduce-unnecessary-treatment-journal-club-jesse-mckenney-cornelia-ding.html
Then there’s This article which discusses how difficult it is to treat intraductal
https://pubmed.ncbi.nlm.nih.gov/40186732/
It’s frustrating to try to help somebody that has both of these things since there are no known solutions.
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5 ReactionsUnfortunately it still comes down to a human reading the slides. And humans will have different opinions. Maybe someday AI will read the slides and other tests (if they don't do already at some places) and give a definitive test result......
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1 Reaction@copyman
Some hospitals like Stanford use AI to double-check mammogram x-rays and yes, it will soon become a norm.
Regarding humans reading slides, yes indeed there is a human factor involved and that is why it is important to ask for second or ever third pair of eyes to check pathology slides ; ).
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2 Reactions@jeffmarc
"It’s frustrating to try to help somebody that has both of these things since there are no known solutions."
Yes, that is why both surgeon and RT suggested taking the gland out and than if anything is left behind could be zapped more easily and thoroughly. I read some papers where they found that somehow IDC cells survive possibly hidden in those ducts - nobody knows why and how, they just found even more weird and much more mutated cells after salvage prostatectomy. I mean, we have NO doubt that we made a good choice with RP since they even found cells that were dying off - just horror all around.
And ALL of that with PSA just 5.4 before surgery ! : ((( Everybody was like "ahhh, take your time, PC grows sloooowww, nor rush, no rush " *blah blah blah and when they took it out was "Oh boy, this was done in the last moment !!! Such aggressive cancer, my goodness... " !!!
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3 ReactionsI was a little confused by the signals I got from every doctor. I was Dx as 3+4. W/cribiform.
John’s Hopkins did 2nd opinion. One core 4+3 w/cribiform.
Treatment at Univ of Cincinnati, they reviewed slides and said 3+4. All said cribiform.
What was strange to me was that Google really said how adverse cribiform was. But the 4 doctors I got opinions from, (1 focal, 2 Ro and one MO never mentioned the cribiform.
When I pushed it, all of the doctors said “it’s a ‘bit’ more aggressive but not so much if IDC isn’t present and testing shows no PTEN loss.
I thought it was a death sentence and they all just kind of glossed over it.
This was after a Decipher which showed a 3% 10 year risk of metastasis and
- PTEN Intact
- very low hypoxia (very responsive to radiation)
- very low emt signal
Basically they all said I had a tumor with a very poor environment to proliferate. Even with cribiform.
@bearcat998 Yes, docs can seem blasé over a word that scares us to death; that simply comes from experience and the outcomes that they themselves have witnessed.
Also, there’s not exactly a Greek diner menu of treatments available, right? I mean you can almost count them on one hand, with perhaps a minor variation thrown in; so they are gonna treat a certain way no matter what, throw in a little ADT, vary how long you’re on it and go from there. To them it’s almost boring…
Phil
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1 Reaction@bearcat998
If it is not large cribriform (over .25 mm) That is not nearly as risky. That may be why the doctors are not concerned about it.
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