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Cribriform pattern disease over‐represented in pelvic lymph node metastases identified on (68)GA PSMA‐PET/CT

OBJECTIVES: To determine whether any specific histologic subtype of prostate cancer was preferentially represented in pelvic lymph node metastases identified on (68)GA‐PSMA‐PET/CT. SUBJECTS AND METHODS: A consecutive series of 66 men with biochemical recurrent prostate cancer was evaluated with (68)...

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Autores principales: Bolton, Damien, Hong, Anne, Papa, Nathan, Perera, Marlon, Kelly, Brian, Duncan, Catriona, Clouston, David, Lawrentschuk, Nathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349597/
https://www.ncbi.nlm.nih.gov/pubmed/35950036
http://dx.doi.org/10.1002/bco2.151
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author Bolton, Damien
Hong, Anne
Papa, Nathan
Perera, Marlon
Kelly, Brian
Duncan, Catriona
Clouston, David
Lawrentschuk, Nathan
author_facet Bolton, Damien
Hong, Anne
Papa, Nathan
Perera, Marlon
Kelly, Brian
Duncan, Catriona
Clouston, David
Lawrentschuk, Nathan
author_sort Bolton, Damien
collection PubMed
description OBJECTIVES: To determine whether any specific histologic subtype of prostate cancer was preferentially represented in pelvic lymph node metastases identified on (68)GA‐PSMA‐PET/CT. SUBJECTS AND METHODS: A consecutive series of 66 men with biochemical recurrent prostate cancer was evaluated with (68)GA‐PSMA‐PET/CT. Where disease was confined to pelvic lymph nodes, patients were offered salvage extended pelvic lymph node dissection. Twenty patients ultimately proceeded to extended bilateral template pelvic lymph node dissection. Lymph node positivity and the histologic subtype of apparent cancer were assessed, as was PSA response to this intervention. RESULTS: Mean PSA at time of PSMA scanning for patients undergoing lymphadenectomy was 2.49 (n = 20, range 0.21–12.0). In 16 of 20 patients, there was evidence of metastatic cribriform pattern prostate cancer in excised nodes (100% cribriform pattern in 11/16). Only four of 20 patients had no evidence of this histologic subtype of disease. PSA response was not related to the presence or proportional amount of cribriform pattern disease identified. CONCLUSIONS: Cribriform pattern adenocarcinoma appears to be the histologic subtype preferentially identified in pelvic lymph nodes on (68)GA‐PSMA‐PET/CT. The use of PSMA‐PET may be particularly valuable in staging of primary or biochemically recurrent prostate cancer in patients with cribriform pattern disease detected on initial biopsy or radical prostatectomy. Further research is required to further confirm the observed association.
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spelling pubmed-93495972022-08-09 Cribriform pattern disease over‐represented in pelvic lymph node metastases identified on (68)GA PSMA‐PET/CT Bolton, Damien Hong, Anne Papa, Nathan Perera, Marlon Kelly, Brian Duncan, Catriona Clouston, David Lawrentschuk, Nathan BJUI Compass To the Drawing Board OBJECTIVES: To determine whether any specific histologic subtype of prostate cancer was preferentially represented in pelvic lymph node metastases identified on (68)GA‐PSMA‐PET/CT. SUBJECTS AND METHODS: A consecutive series of 66 men with biochemical recurrent prostate cancer was evaluated with (68)GA‐PSMA‐PET/CT. Where disease was confined to pelvic lymph nodes, patients were offered salvage extended pelvic lymph node dissection. Twenty patients ultimately proceeded to extended bilateral template pelvic lymph node dissection. Lymph node positivity and the histologic subtype of apparent cancer were assessed, as was PSA response to this intervention. RESULTS: Mean PSA at time of PSMA scanning for patients undergoing lymphadenectomy was 2.49 (n = 20, range 0.21–12.0). In 16 of 20 patients, there was evidence of metastatic cribriform pattern prostate cancer in excised nodes (100% cribriform pattern in 11/16). Only four of 20 patients had no evidence of this histologic subtype of disease. PSA response was not related to the presence or proportional amount of cribriform pattern disease identified. CONCLUSIONS: Cribriform pattern adenocarcinoma appears to be the histologic subtype preferentially identified in pelvic lymph nodes on (68)GA‐PSMA‐PET/CT. The use of PSMA‐PET may be particularly valuable in staging of primary or biochemically recurrent prostate cancer in patients with cribriform pattern disease detected on initial biopsy or radical prostatectomy. Further research is required to further confirm the observed association. John Wiley and Sons Inc. 2022-04-21 /pmc/articles/PMC9349597/ /pubmed/35950036 http://dx.doi.org/10.1002/bco2.151 Text en © 2022 The Authors. BJUI Compass published by John Wiley & Sons Ltd on behalf of BJU International Company. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle To the Drawing Board
Bolton, Damien
Hong, Anne
Papa, Nathan
Perera, Marlon
Kelly, Brian
Duncan, Catriona
Clouston, David
Lawrentschuk, Nathan
Cribriform pattern disease over‐represented in pelvic lymph node metastases identified on (68)GA PSMA‐PET/CT
title Cribriform pattern disease over‐represented in pelvic lymph node metastases identified on (68)GA PSMA‐PET/CT
title_full Cribriform pattern disease over‐represented in pelvic lymph node metastases identified on (68)GA PSMA‐PET/CT
title_fullStr Cribriform pattern disease over‐represented in pelvic lymph node metastases identified on (68)GA PSMA‐PET/CT
title_full_unstemmed Cribriform pattern disease over‐represented in pelvic lymph node metastases identified on (68)GA PSMA‐PET/CT
title_short Cribriform pattern disease over‐represented in pelvic lymph node metastases identified on (68)GA PSMA‐PET/CT
title_sort cribriform pattern disease over‐represented in pelvic lymph node metastases identified on (68)ga psma‐pet/ct
topic To the Drawing Board
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349597/
https://www.ncbi.nlm.nih.gov/pubmed/35950036
http://dx.doi.org/10.1002/bco2.151
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