# Baseline and Dynamic Neutrophil-to-Lymphocyte Ratio as Prognostic Biomarkers in Metastatic Colorectal Cancer Patients Treated with Panitumumab

**Authors:** Teodor Marian Vancea, Andrada Olivia Tapirdea, Mihai Gabriel Zait, Daniel Sur, Calin Cainap, Claudia Burz

PMC · DOI: 10.3390/jpm16010009 · Journal of Personalized Medicine · 2025-12-31

## TL;DR

This study shows that blood tests measuring neutrophil-to-lymphocyte ratios can predict treatment outcomes in colorectal cancer patients receiving a specific drug.

## Contribution

The study identifies baseline and dynamic NLR as novel low-cost prognostic biomarkers for metastatic CRC patients treated with panitumumab.

## Key findings

- Low baseline NLR is associated with longer progression-free survival in CRC patients.
- Patients with increasing NLR during treatment have better outcomes than those with decreasing NLR.
- Baseline NLR remains independently predictive of survival in multivariate analysis.

## Abstract

Background: Colorectal cancer (CRC) remains a leading cause of cancer mortality worldwide, with epidermal growth factor receptor (EGFR) inhibitors improving outcomes in patients with metastatic CRC (mCRC) harboring KRAS wild-type tumors. Inflammation has emerged as a potential determinant of treatment efficacy, and the neutrophil-to-lymphocyte ratio (NLR) represents an accessible biomarker reflecting the balance between protumoral neutrophils and antitumor lymphocytes. Methods: We conducted a retrospective study of 44 patients with left-sided, KRAS wild-type mCRC treated at the Institute of Oncology “Prof. Dr. Ion Chiricuta” between 2015 and 2024 with first-line FOLFOX/FOLFIRI plus panitumumab. Baseline NLR (bNLR) and NLR after four treatment cycles were assessed, with progression-free survival (PFS) as the primary endpoint. Results: Receiver operating characteristic analysis identified an optimal bNLR cutoff of 3.06 (AUC = 0.78, p = 0.004). Patients with low bNLR (≤3.06) had significantly longer PFS than those with high bNLR (>3.06) (14 vs. 7 months, HR = 2.7, p = 0.002). Notably, patients with a positive ΔNLR (increase during therapy) also demonstrated superior PFS compared to those with a negative ΔNLR (18 vs. 11 months, HR = 0.47, p = 0.022). In multivariate analysis, only bNLR remained independently associated with PFS. Conclusions: These results suggest that both baseline and dynamic NLR may serve as low-cost prognostic biomarkers in mCRC patients treated with anti-EGFR therapy.

## Linked entities

- **Genes:** KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845]
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845] {aka 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** Inflammation (MESH:D007249), CRC (MESH:D015179), cancer (MESH:D009369)
- **Chemicals:** FOLFOX (MESH:C410216), Panitumumab (MESH:D000077544), FOLFIRI (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12843235/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12843235/full.md

## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12843235/full.md

---
Source: https://tomesphere.com/paper/PMC12843235