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Lymphadenectomy during pulmonary metastasectomy: Impact on survival and recurrence
Background and Objectives: Lymphadenectomy during pulmonary metastasectomy (PM) is widely carried out. We assessed the potential benefit on patient survival and tumor recurrence of this practice. Methods: One hundred eighty‐one patients undergoing a first PM were studied. Eighty‐six patients (47.5%)...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771868/ https://www.ncbi.nlm.nih.gov/pubmed/31297837 http://dx.doi.org/10.1002/jso.25635 |
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author | Londero, Francesco Morelli, Angelo Parise, Orlando Grossi, William Crestale, Sara Tetta, Cecilia Johnson, Daniel M. Livi, Ugolino Maessen, Jos G. Gelsomino, Sandro |
author_facet | Londero, Francesco Morelli, Angelo Parise, Orlando Grossi, William Crestale, Sara Tetta, Cecilia Johnson, Daniel M. Livi, Ugolino Maessen, Jos G. Gelsomino, Sandro |
author_sort | Londero, Francesco |
collection | PubMed |
description | Background and Objectives: Lymphadenectomy during pulmonary metastasectomy (PM) is widely carried out. We assessed the potential benefit on patient survival and tumor recurrence of this practice. Methods: One hundred eighty‐one patients undergoing a first PM were studied. Eighty‐six patients (47.5%) underwent lymphadenectomy (L+ group) whereas 95 (52.5%) did not undergo nodal harvesting (L−group). Main outcomes were overall survival (OS) and disease‐free survival (DFS). Median follow‐up was 25 months (interquartile range [IQR], 13‐49). Results: At follow‐up 84 patients (46.4%) died, whereas 97 (53.6%) were still alive with recurrence in 78 patients (43%). There was no difference in 5‐year survival (L+ 30.0% vs L− 43.2%; P = .87) or in the 5‐year cumulative incidence of recurrence (L + 63.2% vs L−80%; P = .07) between the two groups. Multivariable analysis indicated that disease‐free interval (DFI) less than 29 months (P < .001) and lung comorbidities (P = .003) were significant predictors of death. Metastases from non‐small–cell lung cancer increased the risk of lung comorbidities by a factor of 19.8, whereas the risk of DFI less than 29 months was increased nearly 11‐fold. Competing risk regression identified multiple metastases (P = .004), head/neck primary tumor (P = .009), and age less than 67 years (P = .024) as independent risk factors for recurrence. Conclusion: Associated lymphadenectomy showed not to give any additional advantage in terms of survival and recurrence after PM. |
format | Online Article Text |
id | pubmed-6771868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67718682019-10-07 Lymphadenectomy during pulmonary metastasectomy: Impact on survival and recurrence Londero, Francesco Morelli, Angelo Parise, Orlando Grossi, William Crestale, Sara Tetta, Cecilia Johnson, Daniel M. Livi, Ugolino Maessen, Jos G. Gelsomino, Sandro J Surg Oncol Research Articles Background and Objectives: Lymphadenectomy during pulmonary metastasectomy (PM) is widely carried out. We assessed the potential benefit on patient survival and tumor recurrence of this practice. Methods: One hundred eighty‐one patients undergoing a first PM were studied. Eighty‐six patients (47.5%) underwent lymphadenectomy (L+ group) whereas 95 (52.5%) did not undergo nodal harvesting (L−group). Main outcomes were overall survival (OS) and disease‐free survival (DFS). Median follow‐up was 25 months (interquartile range [IQR], 13‐49). Results: At follow‐up 84 patients (46.4%) died, whereas 97 (53.6%) were still alive with recurrence in 78 patients (43%). There was no difference in 5‐year survival (L+ 30.0% vs L− 43.2%; P = .87) or in the 5‐year cumulative incidence of recurrence (L + 63.2% vs L−80%; P = .07) between the two groups. Multivariable analysis indicated that disease‐free interval (DFI) less than 29 months (P < .001) and lung comorbidities (P = .003) were significant predictors of death. Metastases from non‐small–cell lung cancer increased the risk of lung comorbidities by a factor of 19.8, whereas the risk of DFI less than 29 months was increased nearly 11‐fold. Competing risk regression identified multiple metastases (P = .004), head/neck primary tumor (P = .009), and age less than 67 years (P = .024) as independent risk factors for recurrence. Conclusion: Associated lymphadenectomy showed not to give any additional advantage in terms of survival and recurrence after PM. John Wiley and Sons Inc. 2019-07-11 2019-09-15 /pmc/articles/PMC6771868/ /pubmed/31297837 http://dx.doi.org/10.1002/jso.25635 Text en © 2019 The Authors. Journal of Surgical Oncology Published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Londero, Francesco Morelli, Angelo Parise, Orlando Grossi, William Crestale, Sara Tetta, Cecilia Johnson, Daniel M. Livi, Ugolino Maessen, Jos G. Gelsomino, Sandro Lymphadenectomy during pulmonary metastasectomy: Impact on survival and recurrence |
title | Lymphadenectomy during pulmonary metastasectomy: Impact on survival and recurrence |
title_full | Lymphadenectomy during pulmonary metastasectomy: Impact on survival and recurrence |
title_fullStr | Lymphadenectomy during pulmonary metastasectomy: Impact on survival and recurrence |
title_full_unstemmed | Lymphadenectomy during pulmonary metastasectomy: Impact on survival and recurrence |
title_short | Lymphadenectomy during pulmonary metastasectomy: Impact on survival and recurrence |
title_sort | lymphadenectomy during pulmonary metastasectomy: impact on survival and recurrence |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771868/ https://www.ncbi.nlm.nih.gov/pubmed/31297837 http://dx.doi.org/10.1002/jso.25635 |
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