# The Predictive Value of Clinical and Systemic Inflammatory Biomarkers in Emergency Colic Cancer Surgery: A Retrospective Study

**Authors:** Adrian Marius Silaghi, Crenguta Sorina Serboiu, Dragos Serban, Vlad Denis Constantin, Corneliu Tudor, Ion Motofei, Gebran Hussein, Paul Lorin Stoica, Marina Ionela Nedea, Ana Maria Dascalu, Tudor Mihai Badescu

PMC · DOI: 10.3390/jcm15041627 · Journal of Clinical Medicine · 2026-02-20

## TL;DR

This study shows that pre-surgery inflammation markers can predict serious complications and death after emergency colon cancer surgery.

## Contribution

The study introduces a multivariate model combining inflammatory biomarkers and comorbidities to predict adverse outcomes in emergency colon cancer surgery.

## Key findings

- CRP, NLR, and PLR are strong predictors of severe postoperative complications.
- A model including CCI, CRP, PLR, and diabetes accurately predicts Clavien–Dindo ≥ IIIA complications.
- PLR, creatinine, and diabetes are independent predictors of anastomotic leak.

## Abstract

Background/Objectives: Emergency surgery for complicated colon cancer carries high morbidity and mortality, largely driven by systemic inflammation and organ dysfunction. This study aims to investigate the predictive value of preoperative inflammatory biomarkers for postoperative outcomes. Methods: We retrospectively analyzed 219 patients undergoing emergency surgery for complicated colon cancer. Patients were classified as uncomplicated (n = 164) or complicated (Clavien–Dindo ≥ IIIA; n = 55). Preoperative clinical data, comorbidity indices, laboratory values, and inflammatory markers: C-reactive protein (CRP), neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and systemic immune-inflammation index (SII) were assessed. Logistic regression and ROC (Receiver Operating Characteristic) curves analyses identified predictors of Clavien Dindo complications graded as IIIA or higher, anastomotic leak (AL), and in-hospital mortality. Results: Most patients included in the study were males (75.02%), with a mean age of 69.63 (±11.54) years. Patients included in the complicated group had higher comorbidity burden, ASA (American Society of Anesthesiologists) grade, rates of diabetes, organ failure, and systemic inflammatory response. All inflammatory biomarkers were significantly elevated in the complicated group (p < 0.001). CRP (>62.8 mg/dL), NLR (>6.89), and PLR (>334.2) showed good discrimination for Clavien Dindo complications graded as IIIA or higher, with AUC (area under curve) ranging from 0.726 to 0.799. A multivariable model including Charlson Comorbidity Index (CCI), CRP, PLR, and diabetes predicted Clavien–Dindo ≥ IIIA complications with excellent accuracy (AUC 0.870). PLR, creatinine, and diabetes independently predicted AL (AUC 0.834). Mortality (20.5%) was strongly associated with peritonitis, CRP, and NLR (AUC 0.891). Conclusions: Preoperative inflammatory biomarkers, combined with comorbidity and renal function, reliably predict adverse outcomes after emergency colon cancer surgery. Multivariate models may be useful for early risk stratification and support individualized perioperative management.

## Linked entities

- **Diseases:** colon cancer (MONDO:0002032)

## Full-text entities

- **Genes:** BCHE (butyrylcholinesterase) [NCBI Gene 590] {aka BCHED, CHE1, CHE2, E1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, F3 (coagulation factor III, tissue factor) [NCBI Gene 2152] {aka CD142, TF, TFA}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, SERPINE1 (serpin family E member 1) [NCBI Gene 5054] {aka PAI, PAI-1, PAI1, PLANH1}
- **Diseases:** bowel obstruction (MESH:D012778), Comorbidity (MESH:D004194), injury to (MESH:D014947), Inflammation (MESH:D007249), -Dindo complications (MESH:D008107), NLR (MESH:D015467), cirrhosis (MESH:D005355), seroma (MESH:D049291), critically ill (MESH:D016638), pain (MESH:D010146), vascular impairment (MESH:D020141), inflammatory syndrome (MESH:D018746), diabetes (MESH:D003920), adenopathy (MESH:D000072281), Colic Cancer (MESH:D009369), primary colic adenocarcinomas (MESH:D000230), chronic kidney disease (MESH:D051436), colon and gastric cancer (MESH:D013274), organ dysfunction (MESH:D009102), autoimmune diseases (MESH:D001327), hemorrhage (MESH:D006470), AKI (MESH:D058186), oncogenic (MESH:D000074723), colic malignancies (MESH:D003085), ischemia (MESH:D007511), Acute Physiology (MESH:D000208), CCI (MESH:C566784), anemia (MESH:D000740), metastases (MESH:D009362), thrombosis (MESH:D013927), obstructive disease (MESH:D001157), Mortality (MESH:D003643), Colon cancer (MESH:D015179), CD (MESH:D003424), infection (MESH:D007239), T (MESH:D001260), postoperative complication (MESH:D011183), Peritonitis (MESH:D010538), AL (MESH:D057868), leaks (MESH:D019559), N (MESH:C536108), urinary infection (MESH:D014552), Health (OMIM:603663), membranous dysfunction (MESH:D015433), type 2 diabetes mellitus (MESH:D003924), bacterial infections (MESH:D001424), organ (MESH:D000092124), impaired renal function (MESH:D007674), SSIs (MESH:D013530), gastrointestinal malignancies (MESH:D005770), postoperative (MESH:D019106), perforation (MESH:D057112), Systemic (MESH:D015619), septic shock (MESH:D012772), gangrene (MESH:D005734), gastrointestinal bleeding (MESH:D006471), ganglion (MESH:D045888), Sepsis (MESH:D018805)
- **Chemicals:** oxygen (MESH:D010100), blood sugar (MESH:D001786), hematoxylin (MESH:D006416), urea (MESH:D014508), lipopolysaccharides (MESH:D008070), eosin (MESH:D004801), creatinine (MESH:D003404), glucose (MESH:D005947), reactive oxygen species (MESH:D017382)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

74 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942449/full.md

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Source: https://tomesphere.com/paper/PMC12942449