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ORIGINAL RESEARCH article

Front. Nutr.

Sec. Clinical Nutrition

Volume 12 - 2025 | doi: 10.3389/fnut.2025.1670597

Prognostic Value of the Modified Systemic Inflammation Score in Stage I-III Colorectal Cancer: A Comparison with Other Inflammation-Based Indices

Provisionally accepted
Kuan  WangKuan Wang1*Boxiang  ZhangBoxiang Zhang1Kejin  LiKejin Li2Ziyi  ZhangZiyi Zhang1Xiangyue  ZengXiangyue Zeng1Binlin  MaBinlin Ma3Wu  ZhiminWu Zhimin4Yipeng  PanYipeng Pan5Lucy  Yue LauLucy Yue Lau6Zeliang  ZhaoZeliang Zhao1*Yi  ChenYi Chen1*
  • 1Cancer Hospital of Xinjiang Medical University, Urumqi, China
  • 2Southern Medical University Nanfang Hospital, Guangzhou, China
  • 3Bortala Mongolian Autonomous Prefecture People's Hospital, Bole, China
  • 4The Maternal and Child Health Care Hospital of Guizhou Medical University, Guizhou, China
  • 5Zhejiang University School of Medicine Sir Run Run Shaw Hospital, Hangzhou, China
  • 6Harvard Medical School, Boston, United States

The final, formatted version of the article will be published soon.

Background Colorectal cancer (CRC) remains one of the leading causes of cancer-related mortality worldwide, and poor postoperative prognosis significantly compromises patients' quality of life. Numerous inflammation-based biomarkers have been reported to predict survival outcomes in CRC patients. However, the prognostic value of the modified Systemic Inflammation Score (mSIS) in long-term outcome prediction following CRC surgery has not yet been fully established. This study aimed to evaluate the prognostic significance of mSIS—constructed using the neutrophil-to-lymphocyte ratio (NLR) and albumin levels—in predicting postoperative survival in CRC patients and to compare its predictive performance with other commonly used inflammation-related markers. Methods We retrospectively analyzed the clinical data of 489 CRC patients from two hospitals, with one institution serving as the validation cohort. Receiver operating characteristic (ROC) curve analysis was performed to determine the optimal cut-off values for pre-treatment systemic inflammation markers and to compare the AUC among various inflammatory indicators. The association between the mSIS and overall survival (OS) was evaluated using Kaplan–Meier survival curves and multivariate Cox regression analysis. Based on the results of the multivariate analysis, a nomogram model was constructed and externally validated. Results The optimal cut-off values for the NLR and serum albumin were determined to be 2.96 and 38.95 g/L, respectively, using the Youden index. High NLR and low albumin levels were independently associated with poorer OS. By combining NLR and albumin levels, we established a mSIS, which stratified patients into low-, intermediate-, and high-risk groups. In the training cohort, the 5-year OS rates were 93.75%, 61.26%, and 18.18%, respectively. The prognostic accuracy of mSIS surpassed that of either marker used alone. mSIS demonstrated a significantly higher AUC for predicting survival outcomes, and the nomogram model constructed based on multivariate Cox regression analysis exhibited superior prognostic discrimination. Conclusion Our study demonstrates that the mSIS can serve as an effective and accessible prognostic tool for stratifying stage I–III CRC patients after surgery and optimizing individualized treatment strategies.

Keywords: colorectal cancer, overall survival, prognosis, nomogram, Serum Albumin

Received: 21 Jul 2025; Accepted: 20 Oct 2025.

Copyright: © 2025 Wang, Zhang, Li, Zhang, Zeng, Ma, Zhimin, Pan, Lau, Zhao and Chen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Kuan Wang, 1565184787@qq.com
Zeliang Zhao, zlzhao71@163.com
Yi Chen, chenyicsu@outlook.com

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