Published online Oct 27, 2024. doi: 10.4240/wjgs.v16.i10.3371
Revised: August 21, 2024
Accepted: August 29, 2024
Published online: October 27, 2024
Processing time: 185 Days and 3.8 Hours
This commentary evaluates the study by Liu et al. This study investigates the predictive utility of the neutrophil-lymphocyte ratio, platelet-lymphocyte ratio, systemic immune-inflammation index, and carcinoembryonic antigen levels for post-operative intra-abdominal infection following colorectal cancer (CRC) surge
Core Tip: This commentary highlights the pioneering study by Liu et al on the use of the neutrophil-lymphocyte ratio, platelet-lymphocyte ratio, systemic immune-inflammation index, and carcinoembryonic antigen as predictive markers for postoperative intra-abdominal infection in colorectal cancer (CRC) patients. This study underscores the need for broadening the patient demographics, intensifying the examination of confounding variables, and the crucial need for prospective validation to ensure the clinical applicability of these markers. Additionally, further research should include multicenter trials and the exploration of additional biomarkers to increase the model's predictive accuracy and clinical relevance. This study also highlights the importance of integrating predictive models into clinical workflows, making them user-friendly for healthcare professionals, and thereby optimizing patient outcomes in CRC management.
- Citation: Zhang SY, Chen J, Cai N. Evaluation of preoperative blood markers for predicting intra-abdominal infection during colorectal cancer resection: A commentary on recent findings. World J Gastrointest Surg 2024; 16(10): 3371-3373
- URL: https://www.wjgnet.com/1948-9366/full/v16/i10/3371.htm
- DOI: https://dx.doi.org/10.4240/wjgs.v16.i10.3371
We read with interest the study by Liu et al[1]. on the predictive value of the neutrophil-lymphocyte ratio (NLR), platelet-lymphocyte ratio (PLR), systemic immune-inflammation index (SII), and carcinoembryonic antigen (CEA) for postope
The meticulous approach to correlate preoperative blood markers with postoperative IAI outcomes highlights an essential area of surgical oncology that merits further exploration. Notably, the study’s methodology, involving a patient cohort and the application of robust statistical analyses, provides a solid foundation for the proposed predictive model. These findings underscore the potential of the NLR, PLR, SII, and CEA as viable predictors for IAI, which could guide preoperative assessments and postoperative strategies, thereby enhancing patient outcomes.
However, additional considerations could enhance the study's impact and clinical applicability: Confounding factors: While the study acknowledges potential confounders, a more detailed examination of factors such as underlying liver conditions, comorbidities, and varying treatment regimens could offer insights into their impact on the predictive accu
Potential typo in the reporting of ORs with 95%CIs: The authors state, “The results indicated that NLR, PLR, SII, and CEA were risk factors for IAI in patients with CRC after radical resection of CRC (odds ratio > 1, P < 0.05) (Table 3)” in the RESULTS Section (P455); “This study found that NLR, PLR, SII, and CEA levels may be risk factors for IAI in patients with CRC after radical resection.” in the CONCLUSION Section (P459). However, in Table 3, the 95%CIs for the NLR and PLR are listed as follows: the NLR (P = 0.017, OR = 1.199, 95%CI: 0.053-1.750) and the PLR (P = 0.024, OR = 1.978, 95%CI: 0.960-1.997), which approach the null value of 1 for the ORs. Although the upper bounds are correctly above 1, the lower bounds fall below 1, which does not typically strongly support the assertion that the NLR and PLR are risk factors, despite the P values being < 0.05. Recent analyses highlight the nuanced interpretation of ORs and CIs in determining risk factors, underscoring that lower bounds falling below 1 could weaken the argument for a variable being a risk factor[3]. Proposed solutions for these inconsistencies include the following: (1) Reevaluate the data by performing additional analyses, including multivariate adjustments, to control for confounding variables and obtain more precise estimates of the effects of the NLR and PLR; or (2) Increase the sample size to obtain more robust estimates, potentially narrowing the CIs and reinforcing the NLR and PLR as reliable predictors.
A technical suggestion for Table 4: In Table 4, regarding the diagnostic value of the receiver operating characteristic curve evaluation index, the authors could include additional metrics along with the 95%CI to enhance the comprehensibility of the diagnostic index. These metrics could include the sensitivity, specificity, accuracy, diagnostic odds ratio, positive predictive value, negative predictive value, positive likelihood ratio, and negative likelihood ratio. These metrics are crucial for a comprehensive understanding of the diagnostic value, as they provide a more detailed assessment of the model's performance in correctly identifying true positives, true negatives, and the overall diagnostic accuracy[4].
Sample size and single-center nature of the study: The study was conducted with a relatively small sample size of 80 patients at a single center. This limitation might restrict the generalizability of the findings to broader populations with diverse demographic and genetic backgrounds.
Retrospective design: The retrospective nature of the study might introduce selection bias and recall bias. Prospective studies are needed to validate the findings and assess the real-time clinical applicability of the nomogram.
Integration with clinical decision-making: Investigating how the nomogram can be integrated into clinical workflows to aid in decision-making processes would be valuable. Research could focus on developing user-friendly tools or software that clinicians can easily use to assess the risk of IAI in CRC patients.
Exploration of additional biomarkers: The exploration of additional biomarkers, including emerging genetic and molecular markers, could provide deeper insights into the mechanisms underlying IAI post-CRC surgery[5]. This could also help refine the predictive model for better accuracy.
Selection and recall biases: Selection bias could arise because the sample was limited to a single hospital, potentially limiting the generalizability of the findings and possibly overestimating the predictive value of the blood markers. Recall bias is also a concern owing to the study’s retrospective nature, where participants might have inaccurately reported preoperative conditions or events, affecting the observed associations between biomarkers and IAI. To address these biases, future research should include more diverse samples and use prospective designs for more accurate data col
In conclusion, the study by Liu et al[1]. represents a significant step forward in our ability to predict and manage IAI in CRC patients postsurgery. We commend the authors for their contribution and anticipate further research that builds on these findings to improve clinical outcomes for patients with CRC.
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