Had LAPR in beginning of June. Prior to LARP: PSA 6.2, Biopsy: 3+4 with 40% GG4. Histology report after LARP upgraded the cancer to 4+3 with 70% GG4. In addition, Intraductal carcinoma and Cribriform morphology of GG4 is identified. (EPE: negative, SV: negative, bladder neck and lymph vascular invasion: negative, surgical margins: negative, pT2, tumor dimension 14mmx8mm- prostate 36.6ml - 40x50x35mm)
PSA 6 weeks after surgery: <0.1
No lymph node is removed during LARP. Now 3 months later, I am wondering to have a lymph node dissection due to upgrade of cancer and higher risk factor in nomogram (evidencio.com/models/show/1....
The risk factor is 16% which is higher than threshold recommendation values.
Shall I do LN dissection?
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FMOH_N
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However with GG4, there is no guarantee, 50% chance of microscopic spread? and if this is the case then I can prevent it from further spread (of course this is my belief that I can prevent it from further spread, however, not sure whether this is correct or not).
I don´t know how much PSA will increase by cancer in only one LN, especially if the amount is microscopic.
PSMA PET scan will only be available when PSA reaches 0.2.
Cured, because no evidence of disease. You are making up a fictional disease in your mind, causing your own anxiety. Stick to what you know in the present moment.
I was 3+4 and my very experienced surgeon didn't remove any lymph nodes. I trust his judgment. My tumor was also T2 and I've had all undetectable PSA's for five years. I think you should go with the ultrasensitive PSA tests and try not to worry.
No point for it now. It should have been done as part of the RP. The average in Europe is 10-12 nodes, half of them in the States (surgeon's time more expensive there). None, as in your case, not the norm anywhere.
The problem is upgrade of cancer that resulted in higher risk of LN involvement (from 10 to 16%). However, how much I can rely on these monograms that are based on statistical data? Many thanks for your massage.
Forget the nomograms, they are only good for a posteriori mass analyses. Your RP, by eliminating the bulk of your PSA origination, provided you with a 100x magnifying lens. Just use it. Watch your PSA, at least to the 2nd decimal place and when you have had 5-6 time samples derive your PSADT. This will tell you, better than anything else, your most plobable prognosis.
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