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Prognostic value of gender and primary tumor location in metastatic colon cancer
Sex might influence prognosis in patients affected by colorectal cancer. We retrospectively studied a cohort of patients affected by metastatic colon cancer (mCC) stratified by sex and primary tumor location. RAS mutational status was also included in the analysis. Overall, 616 patients met the elig...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10539565/ https://www.ncbi.nlm.nih.gov/pubmed/37781086 http://dx.doi.org/10.7150/jca.85748 |
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author | Grassadonia, Antonino Carletti, Erminia De Luca, Antonella Vici, Patrizia Di Lisa, Francesca Sofia Filomeno, Lorena Cicero, Giuseppe De Lellis, Laura Veschi, Serena Florio, Rosalba Brocco, Davide Di Marino, Pietro Alberti, Saverio Gamucci, Teresa Borrelli, Paola Cama, Alessandro Tinari, Nicola |
author_facet | Grassadonia, Antonino Carletti, Erminia De Luca, Antonella Vici, Patrizia Di Lisa, Francesca Sofia Filomeno, Lorena Cicero, Giuseppe De Lellis, Laura Veschi, Serena Florio, Rosalba Brocco, Davide Di Marino, Pietro Alberti, Saverio Gamucci, Teresa Borrelli, Paola Cama, Alessandro Tinari, Nicola |
author_sort | Grassadonia, Antonino |
collection | PubMed |
description | Sex might influence prognosis in patients affected by colorectal cancer. We retrospectively studied a cohort of patients affected by metastatic colon cancer (mCC) stratified by sex and primary tumor location. RAS mutational status was also included in the analysis. Overall, 616 patients met the eligibility criteria, 261 women and 355 men. Neither gender, nor RAS mutational status influenced overall survival (OS) in the entire population. As expected, patients with right-sided colon cancer (RCC) had a significant shorter OS compared to those with left-sided colon cancer (LCC) (21.3 vs 33.1 months, p= 0.002). When the analysis was performed stratifying for gender, RCC retained worse prognosis among men (OS 20.5 vs 33.9 months, p= 0.008), but not among women (p= 0.132). Similarly, the presence of RAS mutations had no prognostic effect in women, but was significantly associate with shorter survival in men (OS 29.5 vs 33.7 months, p= 0.046). In addition, when comparing clinical outcome of women or men according to sidedness and RAS mutational status, RCC was associated with dismal prognosis only in men with RAS mutated tumor (OS 17.2 vs 32.3 months, p= 0.008). Our study highlights the importance of gender in the outcome of patients with mCC. |
format | Online Article Text |
id | pubmed-10539565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-105395652023-09-30 Prognostic value of gender and primary tumor location in metastatic colon cancer Grassadonia, Antonino Carletti, Erminia De Luca, Antonella Vici, Patrizia Di Lisa, Francesca Sofia Filomeno, Lorena Cicero, Giuseppe De Lellis, Laura Veschi, Serena Florio, Rosalba Brocco, Davide Di Marino, Pietro Alberti, Saverio Gamucci, Teresa Borrelli, Paola Cama, Alessandro Tinari, Nicola J Cancer Research Paper Sex might influence prognosis in patients affected by colorectal cancer. We retrospectively studied a cohort of patients affected by metastatic colon cancer (mCC) stratified by sex and primary tumor location. RAS mutational status was also included in the analysis. Overall, 616 patients met the eligibility criteria, 261 women and 355 men. Neither gender, nor RAS mutational status influenced overall survival (OS) in the entire population. As expected, patients with right-sided colon cancer (RCC) had a significant shorter OS compared to those with left-sided colon cancer (LCC) (21.3 vs 33.1 months, p= 0.002). When the analysis was performed stratifying for gender, RCC retained worse prognosis among men (OS 20.5 vs 33.9 months, p= 0.008), but not among women (p= 0.132). Similarly, the presence of RAS mutations had no prognostic effect in women, but was significantly associate with shorter survival in men (OS 29.5 vs 33.7 months, p= 0.046). In addition, when comparing clinical outcome of women or men according to sidedness and RAS mutational status, RCC was associated with dismal prognosis only in men with RAS mutated tumor (OS 17.2 vs 32.3 months, p= 0.008). Our study highlights the importance of gender in the outcome of patients with mCC. Ivyspring International Publisher 2023-09-04 /pmc/articles/PMC10539565/ /pubmed/37781086 http://dx.doi.org/10.7150/jca.85748 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Grassadonia, Antonino Carletti, Erminia De Luca, Antonella Vici, Patrizia Di Lisa, Francesca Sofia Filomeno, Lorena Cicero, Giuseppe De Lellis, Laura Veschi, Serena Florio, Rosalba Brocco, Davide Di Marino, Pietro Alberti, Saverio Gamucci, Teresa Borrelli, Paola Cama, Alessandro Tinari, Nicola Prognostic value of gender and primary tumor location in metastatic colon cancer |
title | Prognostic value of gender and primary tumor location in metastatic colon cancer |
title_full | Prognostic value of gender and primary tumor location in metastatic colon cancer |
title_fullStr | Prognostic value of gender and primary tumor location in metastatic colon cancer |
title_full_unstemmed | Prognostic value of gender and primary tumor location in metastatic colon cancer |
title_short | Prognostic value of gender and primary tumor location in metastatic colon cancer |
title_sort | prognostic value of gender and primary tumor location in metastatic colon cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10539565/ https://www.ncbi.nlm.nih.gov/pubmed/37781086 http://dx.doi.org/10.7150/jca.85748 |
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