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The different clonal origins of metachronous and synchronous metastases
BACKGROUND: Metastases are the leading cause of mortality in cancer patients. Linear and parallel are the two prominent models of metastatic progression. Metastases can be detected synchronously along with the primary tumor or metachronously, following treatment of localized disease. The aim of the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465669/ https://www.ncbi.nlm.nih.gov/pubmed/37340186 http://dx.doi.org/10.1007/s00432-023-05007-3 |
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author | Gofrit, Ofer N. Gofrit, Ben Roditi, Yuval Popovtzer, Aron Frank, Steve Sosna, Jacob Orevi, Marina Goldberg, S. Nahum |
author_facet | Gofrit, Ofer N. Gofrit, Ben Roditi, Yuval Popovtzer, Aron Frank, Steve Sosna, Jacob Orevi, Marina Goldberg, S. Nahum |
author_sort | Gofrit, Ofer N. |
collection | PubMed |
description | BACKGROUND: Metastases are the leading cause of mortality in cancer patients. Linear and parallel are the two prominent models of metastatic progression. Metastases can be detected synchronously along with the primary tumor or metachronously, following treatment of localized disease. The aim of the study was to determine whether synchronous metastases (SM) and metachronous metastases (MM) differ only in lead-time or stem from different biological processes. MATERIALS AND METHODS: We retrospectively studied the chest CTs of 791 patients inflicted by eleven malignancy types that were treated in our institution in the years 2010–2020. Patient’s population included 396 with SM and 395 with MM. The diameter of 15,427 lung metastases was measured. Clonal origin was deduced from the linear/parallel ratio (LPR)-a computerized analysis of metastases diameters. LPR of 1 suggests pure linear dissemination and − 1 pure parallel. RESULTS: Patients with MM were significantly older (average of 62.9 vs 60.7 years, p = 0.02), and higher percentage of them were males (58.7% vs 51.1%, p = 0.03). Median overall survival of patients with MM and SM was remarkably similar (23 months and 26 months respectively, p = 0.774) when calculated from the time of metastases diagnosis. Parallel dissemination (LPR ≤ 0) was found in 35.4% of patients with MM compared to only 19.8% of the patients with SM (p < 0.00001). CONCLUSION: Patients with SM and MM differ in demography and in clonal origin. Different therapeutic approaches may be considered in these two conditions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00432-023-05007-3. |
format | Online Article Text |
id | pubmed-10465669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-104656692023-08-31 The different clonal origins of metachronous and synchronous metastases Gofrit, Ofer N. Gofrit, Ben Roditi, Yuval Popovtzer, Aron Frank, Steve Sosna, Jacob Orevi, Marina Goldberg, S. Nahum J Cancer Res Clin Oncol Research BACKGROUND: Metastases are the leading cause of mortality in cancer patients. Linear and parallel are the two prominent models of metastatic progression. Metastases can be detected synchronously along with the primary tumor or metachronously, following treatment of localized disease. The aim of the study was to determine whether synchronous metastases (SM) and metachronous metastases (MM) differ only in lead-time or stem from different biological processes. MATERIALS AND METHODS: We retrospectively studied the chest CTs of 791 patients inflicted by eleven malignancy types that were treated in our institution in the years 2010–2020. Patient’s population included 396 with SM and 395 with MM. The diameter of 15,427 lung metastases was measured. Clonal origin was deduced from the linear/parallel ratio (LPR)-a computerized analysis of metastases diameters. LPR of 1 suggests pure linear dissemination and − 1 pure parallel. RESULTS: Patients with MM were significantly older (average of 62.9 vs 60.7 years, p = 0.02), and higher percentage of them were males (58.7% vs 51.1%, p = 0.03). Median overall survival of patients with MM and SM was remarkably similar (23 months and 26 months respectively, p = 0.774) when calculated from the time of metastases diagnosis. Parallel dissemination (LPR ≤ 0) was found in 35.4% of patients with MM compared to only 19.8% of the patients with SM (p < 0.00001). CONCLUSION: Patients with SM and MM differ in demography and in clonal origin. Different therapeutic approaches may be considered in these two conditions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00432-023-05007-3. Springer Berlin Heidelberg 2023-06-20 2023 /pmc/articles/PMC10465669/ /pubmed/37340186 http://dx.doi.org/10.1007/s00432-023-05007-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Gofrit, Ofer N. Gofrit, Ben Roditi, Yuval Popovtzer, Aron Frank, Steve Sosna, Jacob Orevi, Marina Goldberg, S. Nahum The different clonal origins of metachronous and synchronous metastases |
title | The different clonal origins of metachronous and synchronous metastases |
title_full | The different clonal origins of metachronous and synchronous metastases |
title_fullStr | The different clonal origins of metachronous and synchronous metastases |
title_full_unstemmed | The different clonal origins of metachronous and synchronous metastases |
title_short | The different clonal origins of metachronous and synchronous metastases |
title_sort | different clonal origins of metachronous and synchronous metastases |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465669/ https://www.ncbi.nlm.nih.gov/pubmed/37340186 http://dx.doi.org/10.1007/s00432-023-05007-3 |
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