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A retrospective study based on SEER database: not all high-risk factors are equal for stage II colon cancer

BACKGROUND: For stage II colon cancer, understanding of high-risk factors (HRFs) that affect the overall survival (OS) and the benefit of chemotherapy is limited. Meanwhile, no stable predictor can effectively predict OS of stage II colon cancer to date. Our study is aimed to identify HRFs associate...

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Autores principales: Li, Dong, Jiang, Zongze, Xiang, Lili, Yang, Chuanhua, Long, Feiwu, Liu, Wenneng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091032/
https://www.ncbi.nlm.nih.gov/pubmed/35571652
http://dx.doi.org/10.21037/tcr-21-1779
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author Li, Dong
Jiang, Zongze
Xiang, Lili
Yang, Chuanhua
Long, Feiwu
Liu, Wenneng
author_facet Li, Dong
Jiang, Zongze
Xiang, Lili
Yang, Chuanhua
Long, Feiwu
Liu, Wenneng
author_sort Li, Dong
collection PubMed
description BACKGROUND: For stage II colon cancer, understanding of high-risk factors (HRFs) that affect the overall survival (OS) and the benefit of chemotherapy is limited. Meanwhile, no stable predictor can effectively predict OS of stage II colon cancer to date. Our study is aimed to identify HRFs associated with OS of stage II colon cancer, to quantify the risk conferred by each HRF, and to evaluate OS benefit gained by chemotherapy. Meanwhile, we attempt to establish a nomogram model for stage II colon cancer. METHODS: The clinical variables of patients with stage II colon cancer between 2000 and 2018 were retrieved from the Surveillance, Epidemiology, and End Results (SEER) database. Univariate and multivariate analysis were performed to filtered out all the HRFs. We calculated the hazard ratios (HR) and evaluated the survival benefit of adjuvant chemotherapy for each HRF and combinations of HRFs. Then, a nomogram model based on all HRFs was established and verified. RESULTS: A total of 39,103 patients with stage II colon cancer were included. T4b tumors were the highest risk for reduced OS [HR =2.821; 95% confidence interval (CI): 1.949–4.082], mucin-producing tumors (HR =2.412; 95% CI: 1.326–4.388) the second, and lymph node (LN) examined less than 12 (HR =2.200; 95% CI: 1.786–2.710) the third. T4 tumors (HR =0.790; 95% CI: 0.542–1.151), poorly/undifferentiated tumors (HR =0.468; 95% CI: 0.237–0.924), and some combinations of HRFs containing either could benefit from adjuvant chemotherapy. Meanwhile, we established an effective nomogram model based on the identified HRFs. CONCLUSIONS: The study has identified several novel HRFs for stage II colon cancer. Adjuvant chemotherapy has considerable OS benefit for stage II colon cancers with some specific HRFs, and treatment plans need to be individualized. Type and number of HRFs should be taken into consideration when recommending adjuvant chemotherapy. Our new nomogram model has better predictive ability and stability than the tumor-node-metastasis (TNM) stage system of American Joint Committee on Cancer (AJCC) staging system.
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spelling pubmed-90910322022-05-12 A retrospective study based on SEER database: not all high-risk factors are equal for stage II colon cancer Li, Dong Jiang, Zongze Xiang, Lili Yang, Chuanhua Long, Feiwu Liu, Wenneng Transl Cancer Res Original Article BACKGROUND: For stage II colon cancer, understanding of high-risk factors (HRFs) that affect the overall survival (OS) and the benefit of chemotherapy is limited. Meanwhile, no stable predictor can effectively predict OS of stage II colon cancer to date. Our study is aimed to identify HRFs associated with OS of stage II colon cancer, to quantify the risk conferred by each HRF, and to evaluate OS benefit gained by chemotherapy. Meanwhile, we attempt to establish a nomogram model for stage II colon cancer. METHODS: The clinical variables of patients with stage II colon cancer between 2000 and 2018 were retrieved from the Surveillance, Epidemiology, and End Results (SEER) database. Univariate and multivariate analysis were performed to filtered out all the HRFs. We calculated the hazard ratios (HR) and evaluated the survival benefit of adjuvant chemotherapy for each HRF and combinations of HRFs. Then, a nomogram model based on all HRFs was established and verified. RESULTS: A total of 39,103 patients with stage II colon cancer were included. T4b tumors were the highest risk for reduced OS [HR =2.821; 95% confidence interval (CI): 1.949–4.082], mucin-producing tumors (HR =2.412; 95% CI: 1.326–4.388) the second, and lymph node (LN) examined less than 12 (HR =2.200; 95% CI: 1.786–2.710) the third. T4 tumors (HR =0.790; 95% CI: 0.542–1.151), poorly/undifferentiated tumors (HR =0.468; 95% CI: 0.237–0.924), and some combinations of HRFs containing either could benefit from adjuvant chemotherapy. Meanwhile, we established an effective nomogram model based on the identified HRFs. CONCLUSIONS: The study has identified several novel HRFs for stage II colon cancer. Adjuvant chemotherapy has considerable OS benefit for stage II colon cancers with some specific HRFs, and treatment plans need to be individualized. Type and number of HRFs should be taken into consideration when recommending adjuvant chemotherapy. Our new nomogram model has better predictive ability and stability than the tumor-node-metastasis (TNM) stage system of American Joint Committee on Cancer (AJCC) staging system. AME Publishing Company 2022-04 /pmc/articles/PMC9091032/ /pubmed/35571652 http://dx.doi.org/10.21037/tcr-21-1779 Text en 2022 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Li, Dong
Jiang, Zongze
Xiang, Lili
Yang, Chuanhua
Long, Feiwu
Liu, Wenneng
A retrospective study based on SEER database: not all high-risk factors are equal for stage II colon cancer
title A retrospective study based on SEER database: not all high-risk factors are equal for stage II colon cancer
title_full A retrospective study based on SEER database: not all high-risk factors are equal for stage II colon cancer
title_fullStr A retrospective study based on SEER database: not all high-risk factors are equal for stage II colon cancer
title_full_unstemmed A retrospective study based on SEER database: not all high-risk factors are equal for stage II colon cancer
title_short A retrospective study based on SEER database: not all high-risk factors are equal for stage II colon cancer
title_sort retrospective study based on seer database: not all high-risk factors are equal for stage ii colon cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091032/
https://www.ncbi.nlm.nih.gov/pubmed/35571652
http://dx.doi.org/10.21037/tcr-21-1779
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