Abstract
Background
Various systemic inflammatory and nutritional scores have been reported to predict postoperative outcomes. This study aimed to investigate the best systemic inflammatory and nutritional scores in colorectal cancer (CRC) patients who underwent potentially curative resection.
Method
We evaluated 468 consecutive CRC patients in this study. Comparisons of systemic inflammatory and nutritional scores, including the neutrophil to lymphocyte ratio (NLR), platelet to lymphocyte ratio (PLR), prognostic index (PI), prognostic nutritional index (PNI), and modified Glasgow prognostic score (mGPS), were performed using univariate/multivariate analyses for patient survival.
Results
The PNI and mGPS, but not the NLR, PLR, and PI, were significantly associated with overall and relapse-free survival. The mGPS, but not the PNI, was strongly correlated with TNM stage (P < 0.001). Cox multivariate analysis showed that both the PNI and mGPS were exclusive independent prognostic factors for both overall and relapse-free survival (P < 0.001). Furthermore, the PNI status predicted patient survival more clearly than the mGPS in combination with TNM stage.
Conclusions
This study suggests that the PNI and mGPS are useful predictive scores in CRC patients who undergo potentially curative resection, especially the PNI in combination with TNM stage. Routine evaluation of the host status using the scores may be useful in CRC treatment.
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Abbreviations
- CRC:
-
Colorectal cancer
- mGPS:
-
Modified Glasgow prognostic score
- CRP:
-
C-reactive protein
- NLR:
-
Neutrophil to lymphocyte ratio
- PLR:
-
Platelet to lymphocyte ratio
- PI:
-
Prognostic index
- PNI:
-
Prognostic nutritional index
- BMI:
-
Body mass index
- CEA:
-
Carcinoembryonic antigen
- HR:
-
Hazard ratio
- CI:
-
Confidence interval
- OS:
-
Overall survival
- DFS:
-
Disease-free survival
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Tokunaga, R., Sakamoto, Y., Nakagawa, S. et al. Comparison of systemic inflammatory and nutritional scores in colorectal cancer patients who underwent potentially curative resection . Int J Clin Oncol 22, 740–748 (2017). https://doi.org/10.1007/s10147-017-1102-5
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DOI: https://doi.org/10.1007/s10147-017-1102-5