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A Longitudinal Dynamic Change in LMR Can Be a Biomarker for Recurrence in Fusobacterium Nucleatum-Positive Colorectal Cancer Patients.

作者信息

Chen Shan, Chang Wan-Hua, Zhang Jie, Liu Xiao-Yuan, Gao Ting, Qi Xiao-Wei, Cai Dong-Yan, Mao Yong, Lu Ting-Xun

机构信息

Department of Oncology, Affiliated Hospital of Jiangnan University, Wuxi, Jiangsu Province, People's Republic of China.

Department of Gastroenterology, Huaian Hospital of Huaian City, Huai'an, Jiangsu Province, People's Republic of China.

出版信息

J Inflamm Res. 2024 Dec 25;17:11587-11604. doi: 10.2147/JIR.S489432. eCollection 2024.


DOI:10.2147/JIR.S489432
PMID:39737097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11683201/
Abstract

PURPOSE: This study assessed lymphocyte-to-monocyte ratio (LMR) changes to predict postoperative recurrence in Fusobacterium nucleatum-positive (Fn-positive) CRC patients. PATIENTS AND METHODS: Clinical information and paraffin tissue specimens were collected from a retrospective cohort of 332 patients. The abundance of Fn in tumor tissue was measured using a quantitative polymerase chain reaction. We evaluated the prognostic value and diagnostic performance of the dynamic changes of LMR from pre-operative to post-treatment (pr-LMR-po) and the dynamic alterations of LMR from pre-operative to post-treatment to pre-end of follow-up (pr-LMR-f) in predicting recurrence in Fn-positive CRC. RESULTS: In the total cohort and adjuvant therapy group cohort, pr-LMR-po independently predicted recurrence-free survival in Fn-positive CRC patients. In the adjuvant therapy group, pr-LMR-po (High-High vs Low-Low: HR: 3.896, 95% CI: 1.503-10.095, p=0.005) was particularly significant. Meanwhile, pr-LMR-f can serve as a predictive biomarker for Fn-positive CRC recurrence, especially in the adjuvant therapy group cohort where the c-statistic for pr-LMR-f was 0.825 (95% CI: 0.804-0.8251), with a sensitivity of 83.6% and a specificity of 79.3%. Compared to the overall adjuvant therapy group cohort, the prognostic performance of pr-LMR-f was superior in the Fn-positive CRC adjuvant therapy group cohort (AUC: 0.825 VS 0.711). Finally, we constructed a prediction model combining pr-LMR-f and CEA. After internal validation using the bootstrap resampling, the model had an AUC of 0.9295, a sensitivity of 94%, and a specificity of 72.7% in the Fn-positive CRC adjuvant therapy group cohort. CONCLUSION: This study found that pr-LMR-po predicts Fn-positive CRC prognosis, and pr-LMR-f may predict Fn-positive CRC recurrence.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b0/11683201/1693890795f9/JIR-17-11587-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b0/11683201/46a3053b39e5/JIR-17-11587-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b0/11683201/8bf0bde060f6/JIR-17-11587-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b0/11683201/597753076ad1/JIR-17-11587-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b0/11683201/1693890795f9/JIR-17-11587-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b0/11683201/46a3053b39e5/JIR-17-11587-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b0/11683201/8bf0bde060f6/JIR-17-11587-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b0/11683201/597753076ad1/JIR-17-11587-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b0/11683201/1693890795f9/JIR-17-11587-g0004.jpg

相似文献

[1]
A Longitudinal Dynamic Change in LMR Can Be a Biomarker for Recurrence in Fusobacterium Nucleatum-Positive Colorectal Cancer Patients.

J Inflamm Res. 2024-12-25

[2]
Prognostic Value of Combined LMR and CEA Dynamic Monitoring in Postoperative Colorectal Cancer Patients.

J Inflamm Res. 2023-9-22

[3]
Evaluation of antibody level against Fusobacterium nucleatum in the serological diagnosis of colorectal cancer.

Sci Rep. 2016-9-28

[4]
The Role of Cancer-Elicited Inflammatory Biomarkers in Predicting Early Recurrence Within Stage II-III Colorectal Cancer Patients After Curable Resection.

J Inflamm Res. 2021-1-18

[5]
A Simple and Novel Fecal Biomarker for Colorectal Cancer: Ratio of to Probiotics Populations, Based on Their Antagonistic Effect.

Clin Chem. 2018-6-18

[6]
Association Between Fusobacterium nucleatum, Pathway Mutation, and Patient Prognosis in Colorectal Cancer.

Ann Surg Oncol. 2018-7-30

[7]
Fusobacterium nucleatum associates with stages of colorectal neoplasia development, colorectal cancer and disease outcome.

Eur J Clin Microbiol Infect Dis. 2014-8

[8]
Improved diagnosis of colorectal cancer using combined biomarkers including Fusobacterium nucleatum, fecal occult blood, transferrin, CEA, CA19-9, gender, and age.

Cancer Med. 2023-7

[9]
Diagnostic Performance of Intestinal in Colorectal Cancer: A Meta-Analysis.

Chin Med J (Engl). 2018-6-5

[10]
Fusobacterium nucleatum-triggered neutrophil extracellular traps facilitate colorectal carcinoma progression.

J Exp Clin Cancer Res. 2023-9-9

本文引用的文献

[1]
Prognostic Value of Combined LMR and CEA Dynamic Monitoring in Postoperative Colorectal Cancer Patients.

J Inflamm Res. 2023-9-22

[2]
The Pathogenicity of Modulated by Dietary Fibers-A Possible Missing Link between the Dietary Composition and the Risk of Colorectal Cancer.

Microorganisms. 2023-8-3

[3]
Lymphocyte-to-monocyte ratio as a prognostic and potential tumor microenvironment indicator in advanced soft tissue sarcoma treated with first-line doxorubicin therapy.

Sci Rep. 2023-7-3

[4]
Development and validation of a nomogram based on neutrophil-to-lymphocyte ratio and fibrinogen-to-lymphocyte ratio for predicting recurrence of colorectal adenoma.

J Gastrointest Oncol. 2022-10

[5]
Fusobacterium nucleatum, a key pathogenic factor and microbial biomarker for colorectal cancer.

Trends Microbiol. 2023-2

[6]
Circulating Lymphocytes Reflect the Local Immune Response in Patients with Colorectal Carcinoma.

Diagnostics (Basel). 2022-6-7

[7]
Relationship between Fusobacterium nucleatum and antitumor immunity in colorectal cancer liver metastasis.

Cancer Sci. 2021-11

[8]
"Driver-passenger" bacteria and their metabolites in the pathogenesis of colorectal cancer.

Gut Microbes. 2021

[9]
Fecal Fusobacterium nucleatum as a predictor for metachronous colorectal adenoma after endoscopic polypectomy.

J Gastroenterol Hepatol. 2021-10

[10]
Facilitates M2 Macrophage Polarization and Colorectal Carcinoma Progression by Activating TLR4/NF-B/S100A9 Cascade.

Front Immunol. 2021

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