Ann Surg Treat Res.  2019 Apr;96(4):191-200. 10.4174/astr.2019.96.4.191.

Preoperative neutrophil-lymphocyte ratio and CEA is associated with poor prognosis in patients with synchronous colorectal cancer liver metastasis

Affiliations
  • 1Department of Surgery, Soonchunhyang University Cheonan Hospital, Cheonan, Korea. gs2834@schmc.ac.kr
  • 2Department of Surgery, Soonchunhyang University Bucheon Hospital, Bucheon, Korea.

Abstract

PURPOSE
Recently, the neutrophil-to-lymphocyte ratio (NLR), an inflammatory response marker, has been reported to be associated with the prognosis in patients with various type of cancer. However, there have been no studies until now that have explored the prognostic role of combined detection of NLR and CEA in patients with synchronous liver-limited colorectal metastases (sCRLM).
METHODS
Eighty-three patients who histologically diagnosed as sCRLM were selected. Their laboratory and clinical data were collected retrospectively. Using receiver operating characteristic curve analysis, the cutoff value of NLR was calculated based on which patients were assigned to a high NLR (more than 1.94) group and low NLR (less than 1.94) group. A cutoff value of 100 ng/mL for serum CEA level was used in light of the previous literature.
RESULTS
CEA level and Poorly differentiated histology of colon cancer was significantly correlated with high NLR (P = 0.005 and P = 0.048, respectively). The multivariate analysis identified the high NLR as independent prognostic factors for OS and DFS in all patients (P = 0.010 and P = 0.006, respectively). Patients with both low levels of NLR and CEA had a significantly longer OS and DFS (P = 0.026 and P = 0.009, respectively).
CONCLUSION
In conclusion, elevated preoperative NLR is strongly correlated with both survival and recurrence in patients who have been diagnosed with resectable sCRLM. The combination of NLR and CEA level could be a more powerful prognostic marker than NLR alone.

Keyword

Colonic neoplasms; Liver; Metastasis; Neutrophils; Carinoembryonic antigen; Prognosis

MeSH Terms

Colonic Neoplasms
Colorectal Neoplasms*
Humans
Liver*
Multivariate Analysis
Neoplasm Metastasis*
Neutrophils
Prognosis*
Recurrence
Retrospective Studies
ROC Curve

Figure

  • Fig. 1 Kaplan-Meier survival curves for overall survival (OS) and disease-free survival (DFS) in patients with synchronous liver-limited colorectal metastase according to their neutrophil-to-lymphocyte ratio (NLR) and CEA levels. (A) OS according to NLR, (B) DFS according to NLR, (C) OS according to CEA levels, (D) DFS according to CEA levels, (E) OS according to combination of NLR and CEA levels (group 1: both high, group 2: either high, group 3 both low), (F) DFS according to combination of NLR and CEA levels (group 1: both high, group 2: either high, group 3 both low).


Cited by  1 articles

Predicting coexisting thyroid cancer with primary hyperparathyroidism in an endemic region of multinodular goiter: evaluating the effectiveness of preoperative inflammatory markers
Hakan Balbaloglu, Ilhan Tasdoven, Mustafa Cagatay Buyukuysal, Emre Karadeniz, Mustafa Comert, Guldeniz Karadeniz Cakmak
Ann Surg Treat Res. 2023;105(5):290-296.    doi: 10.4174/astr.2023.105.5.290.


Reference

1. Jung KW, Won YJ, Oh CM, Kong HJ, Lee DH, Lee KH, et al. Cancer statistics in Korea: incidence, mortality, survival, and prevalence in 2014. Cancer Res Treat. 2017; 49:292–305.
Article
2. Li Y, Bi X, Zhao J, Huang Z, Zhou J, Li Z, et al. Simultaneous hepatic resection benefits patients with synchronous colorectal cancer liver metastases. Chin J Cancer Res. 2016; 28:528–535.
Article
3. Bertens KA, Hawel J, Lung K, Buac S, Pineda-Solis K, Hernandez-Alejandro R. ALPPS: challenging the concept of unresectability--a systematic review. Int J Surg. 2015; 13:280–287.
4. Sandstrom P, Rosok BI, Sparrelid E, Larsen PN, Larsson AL, Lindell G, et al. ALPPS improves resectability ompared with conventional two-stage hepatectomy in patients with advanced colorectal liver metastasis: results from a Scandinavian Multicenter Randomized Controlled Trial (LIGRO Trial). Ann Surg. 2018; 267:833–840.
5. Ozyalvacli G, Yesil C, Kargi E, Kizildag B, Kilitci A, Yilmaz F. Diagnostic and prognostic importance of the neutrophil lymphocyte ratio in breast cancer. Asian Pac J Cancer Prev. 2014; 15:10363–10366.
Article
6. el Aziz LM. Blood neutrophil-lymphocyte ratio predicts survival in locally advanced cancer stomach treated with neoadjuvant chemotherapy FOLFOX 4. Med Oncol. 2014; 31:311.
Article
7. Stotz M, Gerger A, Eisner F, Szkandera J, Loibner H, Ress AL, et al. Increased neutrophil-lymphocyte ratio is a poor prognostic factor in patients with primary operable and inoperable pancreatic cancer. Br J Cancer. 2013; 109:416–421.
Article
8. Gomez D, Farid S, Malik HZ, Young AL, Toogood GJ, Lodge JP, et al. Preoperative neutrophil-to-lymphocyte ratio as a prognostic predictor after curative resection for hepatocellular carcinoma. World J Surg. 2008; 32:1757–1762.
Article
9. Walsh SR, Cook EJ, Goulder F, Justin TA, Keeling NJ. Neutrophil-lymphocyte ratio as a prognostic factor in colorectal cancer. J Surg Oncol. 2005; 91:181–184.
Article
10. Tang H, Li B, Zhang A, Lu W, Xiang C, Dong J. Prognostic significance of neutrophil-to-lymphocyte ratio in colorectal liver metastasis: a systematic review and meta-analysis. PLoS One. 2016; 11:e0159447.
Article
11. Bukowski J, Gozdz S, Sluszniak J, Kowalski D, Zagala A, Korejba W, et al. Carcinoembryonic antigen (CEA) in the serum of patients with cancer of the colon and rectum. Nowotwory. 1986; 36:181–186.
12. Albanopoulos K, Armakolas A, Konstadoulakis MM, Leandros E, Tsiompanou E, Katsaragakis S, et al. Prognostic significance of circulating antibodies against carcinoembryonic antigen (anti-CEA) in patients with colon cancer. Am J Gastroenterol. 2000; 04. 95(4):1056–1061. Erratum in: Am J Gastroenterol 2009;104:2128.
Article
13. Thomas P, Forse RA, Bajenova O. Carcinoembryonic antigen (CEA) and its receptor hnRNP M are mediators of metastasis and the inflammatory response in the liver. Clin Exp Metastasis. 2011; 28:923–932.
Article
14. Pakdel A, Malekzadeh M, Naghibalhossaini F. The association between preoperative serum CEA concentrations and synchronous liver metastasis in colorectal cancer patients. Cancer Biomark. 2016; 16:245–252.
Article
15. McNally GE, Lloyd DM, Grondona JP. Carcinoembryonic antigen as a prognostic factor in colorectal cancer with liver metastases. J Cancer Ther. 2015; 6:1035–1044.
Article
16. Halazun KJ, Aldoori A, Malik HZ, Al-Mukhtar A, Prasad KR, Toogood GJ, et al. Elevated preoperative neutrophil to lymphocyte ratio predicts survival following hepatic resection for colorectal liver metastases. Eur J Surg Oncol. 2008; 34:55–60.
Article
17. Ding PR, An X, Zhang RX, Fang YJ, Li LR, Chen G, et al. Elevated preoperative neutrophil to lymphocyte ratio predicts risk of recurrence following curative resection for stage IIA colon cancer. Int J Colorectal Dis. 2010; 25:1427–1433.
Article
18. Chiang SF, Hung HY, Tang R, Changchien CR, Chen JS, You YT, et al. Can neutrophilto-lymphocyte ratio predict the survival of colorectal cancer patients who have received curative surgery electively? Int J Colorectal Dis. 2012; 27:1347–1357.
Article
19. Peng HX, Yang L, He BS, Pan YQ, Ying HQ, Sun HL, et al. Combination of preoperative NLR, PLR and CEA could increase the diagnostic efficacy for I-III stage CRC. J Clin Lab Anal. 2017; 31.
Article
20. He W, Yin C, Guo G, Jiang C, Wang F, Qiu H, et al. Initial neutrophil lymphocyte ratio is superior to platelet lymphocyte ratio as an adverse prognostic and predictive factor in metastatic colorectal cancer. Med Oncol. 2013; 30:439.
Article
21. Zhan X, Sun X, Hong Y, Wang Y, Ding K. Combined detection of preoperative neutrophil-to-lymphocyte ratio and CEA as an independent prognostic factor in nonmetastatic patients undergoing colorectal cancer resection is superior to NLR or CEA alone. Biomed Res Int. 2017; 2017:3809464.
Article
22. Park MS, Yi NJ, Son SY, You T, Suh SW, Choi YR, et al. Histopathologic factors affecting tumor recurrence after hepatic resection in colorectal liver metastases. Ann Surg Treat Res. 2014; 87:14–21.
Article
23. Qian BZ. Inflammation fires up cancer metastasis. Semin Cancer Biol. 2017; 47:170–176.
Article
24. Kitamura T, Qian BZ, Pollard JW. Immune cell promotion of metastasis. Nat Rev Immunol. 2015; 15:73–86.
Article
25. Grivennikov SI, Greten FR, Karin M. Immunity, inflammation, and cancer. Cell. 2010; 140:883–899.
Article
26. Cools-Lartigue J, Spicer J, McDonald B, Gowing S, Chow S, Giannias B, et al. Neutrophil extracellular traps sequester circulating tumor cells and promote metastasis. J Clin Invest. 2013; pii: 67484. DOI: 10.1172/JCI67484.
Article
27. Kemik O, Kemik AS, Sumer A, Begenik H, Purisa S, Tuzun S. Human neutrophil peptides 1, 2 and 3 (HNP 1-3): elevated serum levels in colorectal cancer and novel marker of lymphatic and hepatic metastasis. Hum Exp Toxicol. 2013; 32:167–171.
Article
28. Wang D, Dubois RN. The role of COX-2 in intestinal inflammation and colorectal cancer. Oncogene. 2010; 29:781–788.
Article
29. Goldstein MJ, Mitchell EP. Carcinoembryonic antigen in the staging and follow-up of patients with colorectal cancer. Cancer Invest. 2005; 23:338–351.
Article
30. Schmoll HJ, Van Cutsem E, Stein A, Valentini V, Glimelius B, Haustermans K, et al. ESMO Consensus Guidelines for management of patients with colon and rectal cancer. a personalized approach to clinical decision making. Ann Oncol. 2012; 23:2479–2516.
Article
Full Text Links
  • ASTR
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr