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Published in: BMC Cancer 1/2023

Open Access 01-12-2023 | Colon Cancer | Research

The optimal minimum lymph node count for carcinoembryonic antigen elevated colon cancer: a population-based study in the SEER set and External set

Authors: Hao Zhang, Chunlin Wang, Yunxiao Liu, Hanqing Hu, Qingchao Tang, Rui Huang, Meng Wang, Guiyu Wang

Published in: BMC Cancer | Issue 1/2023

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Abstract

Purpose

The aim of this paper was to clarify the optimal minimum number of lymph node for CEA-elevated (≥ 5 ng/ml) colon cancer patients.

Methods

Thirteen thousand two hundred thirty-nine patients from the SEER database and 238 patients from the Second Affiliated Hospital of Harbin Medical University (External set) were identified. For cancer-specific survival (CSS), Kaplan-Meier curves were drawn and data were analyzed using log-rank test. Using X-tile software, the optimal cut-off lymph node count was calculated by the maximal Chi-square value method. Cox regression model was applied to perform survival analysis.

Results

In CEA-elevated colon cancer, 18 nodes were defined as the optimal minimum node. The number of lymph node examined (< 12, 12-17 and ≥ 18) was an independent prognosticator in both SEER set (HR12-17 nodes = 1.329, P <  0.001; HR< 12 nodes = 1.985, P <  0.001) and External set (HR12-17 nodes = 1.774, P <  0.032; HR< 12 nodes = 2.741, P <  0.006). Moreover, the revised 18-node standard could identify more positive lymph nodes compared with the 12-node standard in this population.

Conclusions

With the purpose of favorable long-term survival and accurate nodal stage for CEA-elevated colon cancer patients, the 18-node standard could be regarded as an alternative to the 12-node standard advocated by the ASCO and NCCN guidelines.
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Literature
1.
go back to reference Siegel R, Miller K, Fuchs H, Jemal A. Cancer Statistics, 2021. CA Cancer J Clin. 2021;71(1):7–33.CrossRef Siegel R, Miller K, Fuchs H, Jemal A. Cancer Statistics, 2021. CA Cancer J Clin. 2021;71(1):7–33.CrossRef
2.
go back to reference Gangireddy V, Coleman T, Kanneganti P, Talla S, Annapureddy A, Amin R, et al. Polypectomy versus surgery in early colon cancer: size and location of colon cancer affect long-term survival. Int J Color Dis. 2018;33(10):1349–57.CrossRef Gangireddy V, Coleman T, Kanneganti P, Talla S, Annapureddy A, Amin R, et al. Polypectomy versus surgery in early colon cancer: size and location of colon cancer affect long-term survival. Int J Color Dis. 2018;33(10):1349–57.CrossRef
3.
go back to reference Zhang H, Liu Y, Wang C, Guan Z, Yu H, Xu C, et al. A Modified Tumor-Node-Metastasis Staging System for Colon Cancer Patients with Fewer than Twelve Lymph Nodes Examined. World J Surg. 2021;45(8):2601–9.CrossRef Zhang H, Liu Y, Wang C, Guan Z, Yu H, Xu C, et al. A Modified Tumor-Node-Metastasis Staging System for Colon Cancer Patients with Fewer than Twelve Lymph Nodes Examined. World J Surg. 2021;45(8):2601–9.CrossRef
4.
go back to reference Johnson P, Porter G, Ricciardi R, Baxter N. Increasing negative lymph node count is independently associated with improved long-term survival in stage IIIB and IIIC colon cancer. J Clin Oncol: official journal of the American Society of Clinical Oncology. 2006;24(22):3570–5.CrossRef Johnson P, Porter G, Ricciardi R, Baxter N. Increasing negative lymph node count is independently associated with improved long-term survival in stage IIIB and IIIC colon cancer. J Clin Oncol: official journal of the American Society of Clinical Oncology. 2006;24(22):3570–5.CrossRef
5.
go back to reference Feng H, Lyu Z, Liang W, Cai G, Deng Z, Jiang M, et al. Optimal examined lymph node count in node-negative colon cancer should be determined. Future Oncol. 2021;17(29):3865–72.CrossRef Feng H, Lyu Z, Liang W, Cai G, Deng Z, Jiang M, et al. Optimal examined lymph node count in node-negative colon cancer should be determined. Future Oncol. 2021;17(29):3865–72.CrossRef
6.
go back to reference Benson A, Venook A, Al-Hawary M, Cederquist L, Chen Y, Ciombor K, et al. NCCN Guidelines Insights: Colon Cancer, Version 2.2018. J Nat Comprehensive Cancer Network : JNCCN. 2018;16(4):359–69.CrossRef Benson A, Venook A, Al-Hawary M, Cederquist L, Chen Y, Ciombor K, et al. NCCN Guidelines Insights: Colon Cancer, Version 2.2018. J Nat Comprehensive Cancer Network : JNCCN. 2018;16(4):359–69.CrossRef
7.
go back to reference Gold P, Freedman S. Demonstration of tumor-specific antigens in humsn colonic carcinomata by immunological tolerance and absorption techniques. J Exp Med. 1965;121:439–62.CrossRef Gold P, Freedman S. Demonstration of tumor-specific antigens in humsn colonic carcinomata by immunological tolerance and absorption techniques. J Exp Med. 1965;121:439–62.CrossRef
8.
go back to reference Goldstein M, Mitchell E. Carcinoembryonic antigen in the staging and follow-up of patients with colorectal cancer. Cancer Investig. 2005;23(4):338–51.CrossRef Goldstein M, Mitchell E. Carcinoembryonic antigen in the staging and follow-up of patients with colorectal cancer. Cancer Investig. 2005;23(4):338–51.CrossRef
9.
go back to reference Nakagoe T, Sawai T, Ayabe H, Nakazaki T, Ishikaw H, Hatano K, et al. Prognostic value of carcinoembryonic antigen (CEA) in tumor tissue of patients with colorectal cancer. Anticancer Res. 2001;21:3031–6. Nakagoe T, Sawai T, Ayabe H, Nakazaki T, Ishikaw H, Hatano K, et al. Prognostic value of carcinoembryonic antigen (CEA) in tumor tissue of patients with colorectal cancer. Anticancer Res. 2001;21:3031–6.
10.
go back to reference Carriquiry L, Piñeyro A. Should carcinoembryonic antigen be used in the management of patients with colorectal cancer? Dis Colon Rectum. 1999;42(7):921–9.CrossRef Carriquiry L, Piñeyro A. Should carcinoembryonic antigen be used in the management of patients with colorectal cancer? Dis Colon Rectum. 1999;42(7):921–9.CrossRef
11.
go back to reference Onetto M, Paganuzzi M, Secco G, Fardelli R, Santi F, Rovida S, et al. Preoperative carcinoembryonic antigen and prognosis in patients with colorectal cancer. Biomed Pharmacot = Biomedecine & pharmacotherapie. 1985;39(7):392–5. Onetto M, Paganuzzi M, Secco G, Fardelli R, Santi F, Rovida S, et al. Preoperative carcinoembryonic antigen and prognosis in patients with colorectal cancer. Biomed Pharmacot = Biomedecine & pharmacotherapie. 1985;39(7):392–5.
12.
go back to reference Beauchemin N, Arabzadeh A. Carcinoembryonic antigen-related cell adhesion molecules (CEACAMs) in cancer progression and metastasis. Cancer Metastasis Rev. 2013;32:643–71.CrossRef Beauchemin N, Arabzadeh A. Carcinoembryonic antigen-related cell adhesion molecules (CEACAMs) in cancer progression and metastasis. Cancer Metastasis Rev. 2013;32:643–71.CrossRef
13.
go back to reference Compton C, Fenoglio-Preiser C, Pettigrew N, Fielding L. American Joint Committee on Cancer Prognostic Factors Consensus Conference: Colorectal Working Group. Cancer. 2000;88(7):1739–57.CrossRef Compton C, Fenoglio-Preiser C, Pettigrew N, Fielding L. American Joint Committee on Cancer Prognostic Factors Consensus Conference: Colorectal Working Group. Cancer. 2000;88(7):1739–57.CrossRef
14.
go back to reference Liu Y, Zhang H, Wang Y, Zheng M, Wang C, Hu H, et al. Exploration of a modified stage for pN0 colon cancer patients. Sci Rep. 2022;12(1):5214.CrossRef Liu Y, Zhang H, Wang Y, Zheng M, Wang C, Hu H, et al. Exploration of a modified stage for pN0 colon cancer patients. Sci Rep. 2022;12(1):5214.CrossRef
15.
go back to reference Camp R, Dolled-Filhart M, Rimm D. X-tile: a new bio-informatics tool for biomarker assessment and outcome-based cut-point optimization. Clin Cancer Res: an official journal of the American Association for Cancer Research. 2004;10(21):7252–9.CrossRef Camp R, Dolled-Filhart M, Rimm D. X-tile: a new bio-informatics tool for biomarker assessment and outcome-based cut-point optimization. Clin Cancer Res: an official journal of the American Association for Cancer Research. 2004;10(21):7252–9.CrossRef
16.
go back to reference Guan X, Wang Y, Hu H, Zhao Z, Jiang Z, Liu Z, et al. Reconsideration of the optimal minimum lymph node count for young colon cancer patients: a population-based study. BMC Cancer. 2018;18(1):623.CrossRef Guan X, Wang Y, Hu H, Zhao Z, Jiang Z, Liu Z, et al. Reconsideration of the optimal minimum lymph node count for young colon cancer patients: a population-based study. BMC Cancer. 2018;18(1):623.CrossRef
17.
go back to reference Ning F, Pei J, Zhang N, Wang J, Quan H, Mei Z, et al. Harvest of at least 18 lymph nodes is associated with improved survival in patients with pN0 colon cancer: a retrospective cohort study. J Cancer Res Clin Oncol. 2020;146(8):2117–33.CrossRef Ning F, Pei J, Zhang N, Wang J, Quan H, Mei Z, et al. Harvest of at least 18 lymph nodes is associated with improved survival in patients with pN0 colon cancer: a retrospective cohort study. J Cancer Res Clin Oncol. 2020;146(8):2117–33.CrossRef
18.
go back to reference Cai Y, Cheng G, Lu X, Ju H, Zhu X. The re-evaluation of optimal lymph node yield in stage II right-sided colon cancer: is a minimum of 12 lymph nodes adequate? Int J Color Dis. 2020;35(4):623–31.CrossRef Cai Y, Cheng G, Lu X, Ju H, Zhu X. The re-evaluation of optimal lymph node yield in stage II right-sided colon cancer: is a minimum of 12 lymph nodes adequate? Int J Color Dis. 2020;35(4):623–31.CrossRef
19.
go back to reference Guan X, Chen W, Jiang Z, Liu Z, Miao D, Hu H, et al. Exploration of the Optimal Minimum Lymph Node Count after Colon Cancer Resection for Patients Aged 80 Years and Older. Sci Rep. 2016;6:38901.CrossRef Guan X, Chen W, Jiang Z, Liu Z, Miao D, Hu H, et al. Exploration of the Optimal Minimum Lymph Node Count after Colon Cancer Resection for Patients Aged 80 Years and Older. Sci Rep. 2016;6:38901.CrossRef
20.
go back to reference Nash G, Row D, Weiss A, Shia J, Guillem J, Paty P, et al. A predictive model for lymph node yield in colon cancer resection specimens. Ann Surg. 2011;253(2):318–22.CrossRef Nash G, Row D, Weiss A, Shia J, Guillem J, Paty P, et al. A predictive model for lymph node yield in colon cancer resection specimens. Ann Surg. 2011;253(2):318–22.CrossRef
21.
go back to reference Guan X, Chen W, Liu Z, Jiang Z, Hu H, Zhao Z, et al. Whether regional lymph nodes evaluation should be equally required for both right and left colon cancer. Oncotarget. 2016;7(37):59945–56.CrossRef Guan X, Chen W, Liu Z, Jiang Z, Hu H, Zhao Z, et al. Whether regional lymph nodes evaluation should be equally required for both right and left colon cancer. Oncotarget. 2016;7(37):59945–56.CrossRef
22.
go back to reference He W, Xie Q, Hu W, Kong P, Yang L, Yang Y, et al. An increased number of negative lymph nodes is associated with a higher immune response and longer survival in colon cancer patients. Cancer Manag Res. 2018;10:1597–604.CrossRef He W, Xie Q, Hu W, Kong P, Yang L, Yang Y, et al. An increased number of negative lymph nodes is associated with a higher immune response and longer survival in colon cancer patients. Cancer Manag Res. 2018;10:1597–604.CrossRef
23.
go back to reference Evans M, Barton K, Rees A, Stamatakis J, Karandikar S. The impact of surgeon and pathologist on lymph node retrieval in colorectal cancer and its impact on survival for patients with Dukes' stage B disease. Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland. 2008;10(2):157–64. Evans M, Barton K, Rees A, Stamatakis J, Karandikar S. The impact of surgeon and pathologist on lymph node retrieval in colorectal cancer and its impact on survival for patients with Dukes' stage B disease. Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland. 2008;10(2):157–64.
24.
go back to reference Cai H, He H, Tian W, Zhou M, Hu Y, Deng Y. Colorectal cancer lymph node staining by activated carbon nanoparticles suspension in vivo or methylene blue in vitro. World J Gastroenterol. 2012;18(42):6148–54.CrossRef Cai H, He H, Tian W, Zhou M, Hu Y, Deng Y. Colorectal cancer lymph node staining by activated carbon nanoparticles suspension in vivo or methylene blue in vitro. World J Gastroenterol. 2012;18(42):6148–54.CrossRef
Metadata
Title
The optimal minimum lymph node count for carcinoembryonic antigen elevated colon cancer: a population-based study in the SEER set and External set
Authors
Hao Zhang
Chunlin Wang
Yunxiao Liu
Hanqing Hu
Qingchao Tang
Rui Huang
Meng Wang
Guiyu Wang
Publication date
01-12-2023
Publisher
BioMed Central
Published in
BMC Cancer / Issue 1/2023
Electronic ISSN: 1471-2407
DOI
https://doi.org/10.1186/s12885-023-10524-y

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