Prostate cancer, pathology report after RPR & Lymph nodes removed.
Hi. It's been awhile. My fiance had his surgery, RPR & Lymphendectomy.
The pathology results are so confusing.
We scheduled a PSA for 6 & 12weeks after surgery, per surgeons instructions.
We see the surgeons NP to discuss results but I think a medical oncologist would be very helpful.
The cancer included Cribriform-inside & outside of the prostate, IDC-P, no spread to lymph nodes, spread to bladder neck and other confusing pathology results.
I don't understand most of the acronyms or the doctor speak but we are trying to interpret each part of the report on Pubmed, Mayo, Prostate Cancer.org, etc..
1). I know that genomic testing is very important?
Can anyone explain this to me, in simple terms?
2). What is IDC-P, and what additional questions and tests should be asked for?
3). The surgeon started clear margins but I struggle with this due to the Cribriform outside the prostate, IDC-P and bladder neck spread.
4). PSA before surgery was only around 5.7. Highest Gleason was(3+4=7)-the Cribriform areas.
It's only been about 3 weeks since the surgery. I'm overwhelmed with fear for my boyfriend and lack of information, a very busy care "team", and I need to be equipped with the right information to help him during this life long journey..
I'm sure that I sound scattered but I'm really scared and the surgeon is very confident that, things went well and he should just have his PSA checked in 6 & 12weeks & every 6 months going forward.
This seems a bit simple for such a complex pathology report and from everything I have researched.
Any advice would be greatly appreciated. Please note that I'm just learning the terminology...
And don't get the acronyms very well...
Thanks in advance..
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@surftohealth88
Hi.
Your message means ALOT to me..
The information is paramount for quality of life & to simply not be so stressed from sun up to sundown.
Your understanding & compassion are so refreshing & much needed.🤗
I want to cry & hug you.❤️
Wishing you & your husband well.
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6 Reactions@bikeman1
Hi..
Thank you for getting back. And for the abbreviation PDF...🙂
I hope you enjoyed your ride..
Me & my fiance ride..
But this summer we are talking a break-obviously.😟
Although I wish we could-it's just a few months..
I'm working on getting appts now..
So, fingers crossed..
Thank you for your input & sharing your story & the valuable information..
I hope to report back with positive news & multiple appointments...
Enjoy the ride & Be safe .
❤️Melinda
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2 Reactions@surftohealth88
It’s interesting that the biopsy that she supplied mentions nothing about cribriform Being outside the prostate. It could be the doctor told her that, but it sure isn’t clear from the biopsy.
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1 Reaction@jeffmarc ,
@surftohealth88
Just to clarify.
The surgeon did tell me the cribriform was inside & on the outside lining of the prostate.
Sadly, our discussion about the report was just a Health Chart message & a 15 second voicemail.
Luckily, I have a transcript of the voicemail.
Because he must have been driving & I could only hear cars..
Odd...
But I guess odd & being extremely nonchalant are now common place..
But I will not be steam rolled by an overworked callous surgeon and will get the necessary appts & tests.
Sending love,
Melinda
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5 Reactions@guybe That is great advice, @guybe. You really do need someone outside the box when treatment can be complex.
Like the saying goes, “when all you have is a hammer, everything looks like a nail”
Phil
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3 Reactions@guybe
Thank you..
I've contacted 2 Med. Oncologists today.
I'll wait 48hours & call again..
If it wasn't for this site & doing our own research, we would be completely in the dark..
Wishing you well..❤️
Melinda
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5 Reactions@myboo2u Did you initiate the MO contacts on your own, or get a referral? It was in a meeting with my newly-assigned radiation guy that I asked for a referral to an MO within his organization (Johns Hopkins), and got one. Without that, I might have been at sea, and could have wound up in a situation prone to lack of coordination between RO and MO, if I ever found one at all. With the referral from a source within the COE, I was put on the MO's schedule immediately - though it did take a couple of weeks to meet with him.
Yeah, this site is pretty amazing. The level of detail and variety of experience among the comments are an enormous help. (Thanks, everyone!)
Best of luck in your search!
Guy
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6 ReactionsHi Guy,
How are you?
I don't have a referral for a Medical oncologist or Radiation oncologist.
But the surgeon, also the doctor(I guess), suggested prior to surgery, for us to review the entire "Care team" at the Cancer center & schedule accordingly..
I just called everyone.
And I'm hoping to get a callback.
But I will call again tomorrow, or next week, if no response.
The surgeon didn't take any time to discuss the pathology with us & with multiple red flags in the pathology report, we are not willing to take any chances.
I can't even get anyone from the surgeons office to respond to a health chart message. So-we will try to get things done without the surgeons help.
If things don't work out at the Cancer center or if everyone is just too busy, we will go somewhere else..
I'm slightly shocked, disturbed & angry that no one was able to spend 15minutes with us to discuss the Pathology report in detail.
Scary..
How is your care at Johns Hopkins?
Hope you are having a good day.
Melinda
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3 Reactions