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Results from extended lymphadenectomies with [(111)In]PSMA-617 for intraoperative detection of PSMA-PET/CT-positive nodal metastatic prostate cancer
PURPOSE: Identification of suspicious PSMA-PET/CT-positive lymph node (LN) metastases (LNM) from prostate cancer (PCa) during lymphadenectomy (LA) is challenging. We evaluated an (111)In-labelled PSMA ligand (DKFZ-617, referred to as [(111)In]PSMA-617) as a γ-emitting tracer for intraoperative γ-pro...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060305/ https://www.ncbi.nlm.nih.gov/pubmed/32144598 http://dx.doi.org/10.1186/s13550-020-0598-2 |
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author | Jilg, Cordula A. Reichel, Kathrin Stoykow, Christian Rischke, H. Christian Bartholomä, Mark Drendel, Vanessa von Büren, Moritz Schultze-Seemann, Wolfgang Meyer, Philipp T. Mix, Michael |
author_facet | Jilg, Cordula A. Reichel, Kathrin Stoykow, Christian Rischke, H. Christian Bartholomä, Mark Drendel, Vanessa von Büren, Moritz Schultze-Seemann, Wolfgang Meyer, Philipp T. Mix, Michael |
author_sort | Jilg, Cordula A. |
collection | PubMed |
description | PURPOSE: Identification of suspicious PSMA-PET/CT-positive lymph node (LN) metastases (LNM) from prostate cancer (PCa) during lymphadenectomy (LA) is challenging. We evaluated an (111)In-labelled PSMA ligand (DKFZ-617, referred to as [(111)In]PSMA-617) as a γ-emitting tracer for intraoperative γ-probe application for resected tissue samples in PCa patients. Forty-eight hours prior to LA, [(111)In]PSMA-617 was administered intravenously in 23 patients with suspected LNM on PSMA-PET/CT (n = 21 with biochemical relapse, n = 2 at primary therapy). Resected tissue samples (LN, LNM and fibrofatty tissue) were measured ex situ by a γ-probe expressed as counts per second (CPS(norm)). [(111)In]PSMA-617 tissue sample uptake was measured by a germanium detector for verification and calculated as %IA(lbm) (percent injected activity per kilogram lean body mass at time of surgery). Based on a clinical requirement for a specificity > 95%, thresholds for both ex situ measurements were chosen accordingly. Correlation of the results from PET/CT, γ-probe and germanium detector with histopathology was done. RESULTS: Eight hundred sixty-four LNs (197 LNM) were removed from 275 subregions in 23 patients, on average 8.6 ± 14.9 LNM per patient. One hundred four of 275 tissue samples showed cancer. Median γ-probe and germanium detector results were significantly different between tumour-affected (33.5 CPS(norm), 0.71 %IA(lbm)) and tumour-free subregions (3.0 CPS(norm), 0.03 %IA(lbm)) (each p value < 0.0001). For the chosen γ-probe cut-off (CPS(norm) > 23) and germanium detector cut-off (%IA(lbm) > 0.27), 64 and 74 true-positive and 158 true-negative samples for both measurements were identified. Thirty-nine and 30 false-negative and 6 and 5 false-positive tissue samples were identified by γ-probe and germanium detector measurements. CONCLUSION: [(111)In]PSMA-617 application for LA is feasible in terms of an intraoperative real-time measurement with a γ-probe for detection of tumour-affected tissue samples. γ-probe results can be confirmed by precise germanium detector measurements and were significantly different between tumour-affected and tumour-free samples. |
format | Online Article Text |
id | pubmed-7060305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-70603052020-03-23 Results from extended lymphadenectomies with [(111)In]PSMA-617 for intraoperative detection of PSMA-PET/CT-positive nodal metastatic prostate cancer Jilg, Cordula A. Reichel, Kathrin Stoykow, Christian Rischke, H. Christian Bartholomä, Mark Drendel, Vanessa von Büren, Moritz Schultze-Seemann, Wolfgang Meyer, Philipp T. Mix, Michael EJNMMI Res Original Research PURPOSE: Identification of suspicious PSMA-PET/CT-positive lymph node (LN) metastases (LNM) from prostate cancer (PCa) during lymphadenectomy (LA) is challenging. We evaluated an (111)In-labelled PSMA ligand (DKFZ-617, referred to as [(111)In]PSMA-617) as a γ-emitting tracer for intraoperative γ-probe application for resected tissue samples in PCa patients. Forty-eight hours prior to LA, [(111)In]PSMA-617 was administered intravenously in 23 patients with suspected LNM on PSMA-PET/CT (n = 21 with biochemical relapse, n = 2 at primary therapy). Resected tissue samples (LN, LNM and fibrofatty tissue) were measured ex situ by a γ-probe expressed as counts per second (CPS(norm)). [(111)In]PSMA-617 tissue sample uptake was measured by a germanium detector for verification and calculated as %IA(lbm) (percent injected activity per kilogram lean body mass at time of surgery). Based on a clinical requirement for a specificity > 95%, thresholds for both ex situ measurements were chosen accordingly. Correlation of the results from PET/CT, γ-probe and germanium detector with histopathology was done. RESULTS: Eight hundred sixty-four LNs (197 LNM) were removed from 275 subregions in 23 patients, on average 8.6 ± 14.9 LNM per patient. One hundred four of 275 tissue samples showed cancer. Median γ-probe and germanium detector results were significantly different between tumour-affected (33.5 CPS(norm), 0.71 %IA(lbm)) and tumour-free subregions (3.0 CPS(norm), 0.03 %IA(lbm)) (each p value < 0.0001). For the chosen γ-probe cut-off (CPS(norm) > 23) and germanium detector cut-off (%IA(lbm) > 0.27), 64 and 74 true-positive and 158 true-negative samples for both measurements were identified. Thirty-nine and 30 false-negative and 6 and 5 false-positive tissue samples were identified by γ-probe and germanium detector measurements. CONCLUSION: [(111)In]PSMA-617 application for LA is feasible in terms of an intraoperative real-time measurement with a γ-probe for detection of tumour-affected tissue samples. γ-probe results can be confirmed by precise germanium detector measurements and were significantly different between tumour-affected and tumour-free samples. Springer Berlin Heidelberg 2020-03-06 /pmc/articles/PMC7060305/ /pubmed/32144598 http://dx.doi.org/10.1186/s13550-020-0598-2 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Jilg, Cordula A. Reichel, Kathrin Stoykow, Christian Rischke, H. Christian Bartholomä, Mark Drendel, Vanessa von Büren, Moritz Schultze-Seemann, Wolfgang Meyer, Philipp T. Mix, Michael Results from extended lymphadenectomies with [(111)In]PSMA-617 for intraoperative detection of PSMA-PET/CT-positive nodal metastatic prostate cancer |
title | Results from extended lymphadenectomies with [(111)In]PSMA-617 for intraoperative detection of PSMA-PET/CT-positive nodal metastatic prostate cancer |
title_full | Results from extended lymphadenectomies with [(111)In]PSMA-617 for intraoperative detection of PSMA-PET/CT-positive nodal metastatic prostate cancer |
title_fullStr | Results from extended lymphadenectomies with [(111)In]PSMA-617 for intraoperative detection of PSMA-PET/CT-positive nodal metastatic prostate cancer |
title_full_unstemmed | Results from extended lymphadenectomies with [(111)In]PSMA-617 for intraoperative detection of PSMA-PET/CT-positive nodal metastatic prostate cancer |
title_short | Results from extended lymphadenectomies with [(111)In]PSMA-617 for intraoperative detection of PSMA-PET/CT-positive nodal metastatic prostate cancer |
title_sort | results from extended lymphadenectomies with [(111)in]psma-617 for intraoperative detection of psma-pet/ct-positive nodal metastatic prostate cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060305/ https://www.ncbi.nlm.nih.gov/pubmed/32144598 http://dx.doi.org/10.1186/s13550-020-0598-2 |
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