# Unlocking the predictive value of post-neoadjuvant immune biomarkers in breast cancer: neutrophil-to-lymphocyte ratio (NLR) and systemic immune-inflammation index (SII)

**Authors:** María Esperanza Guirao García, Pedro Marín Rodríguez, Carmen María Servet Pérez de Lema, Noel Blaya Boluda, Pilar Sánchez Henarejos, Miguel Ángel Moya Hernández, Andrea Gottlob Pérez, Caridad Marín Hernández, Pilar de la Morena Barrio, Elisa García Garre, Elena García-Martínez, Francisco Ayala de la Peña, Antonio Piñero Madrona, Esmeralda García-Torralba

PMC · DOI: 10.1007/s10549-026-07928-2 · Breast Cancer Research and Treatment · 2026-03-16

## TL;DR

This study explores how immune biomarkers like NLR and SII after chemotherapy relate to breast cancer outcomes, finding some links to treatment response but not survival.

## Contribution

The study introduces post-neoadjuvant NLR and SII as potential predictors of pathological complete response in breast cancer.

## Key findings

- Post-neoadjuvant NLR and SII are independently associated with pathological complete response.
- Baseline NLR and SII correlate with patient characteristics like age and cancer subtype.
- Neither biomarker significantly impacts overall or progression-free survival.

## Abstract

To evaluate the potential prognostic value of two peripheral immune biomarkers—neutrophil-to-lymphocyte ratio (NLR) and systemic immune-inflammation index (SII)—in breast cancer patients treated with neoadjuvant chemotherapy, and to assess their association with pathological complete response (pCR) and other predictive factors. In addition, to determine whether prognostic or predictive differences exist between baseline and post-neoadjuvant values of these biomarkers.

We analyzed 801 women with early breast cancer treated with neoadjuvant chemotherapy, evaluating clinical and pathological data, survival outcomes, NLR (continuous and categorical) and SII.

Baseline NLR was significantly higher in younger patients, in those with positive pathological nodes, and in the HER2 + /HR − subtype, while baseline SII was elevated in the triple-negative subtype. Post-neoadjuvant chemotherapy (post-NCT) NLR and SII showed only weak associations with estrogen receptor expression, yet both were independently associated with pCR (post-NCT NLR: OR = 0.91; 95% CI: 0.84–0.98; p = 0.02; post-NCT SII: OR = 0.65; 95% CI: 0.47–0.89; p = 0.008). Neither biomarker showed a significant impact on overall or progression-free survival.

Post-treatment NLR and SII may reflect chemotherapy-induced immune changes and are associated with pathological complete response, but their additional predictive value is uncertain, and no prognostic impact was observed.

The online version contains supplementary material available at 10.1007/s10549-026-07928-2.

## Linked entities

- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}
- **Diseases:** SII (MESH:D007249), BC (MESH:D001943), immune (MESH:D007154), NLR (MESH:D015467), ALC (MESH:D009845), death (MESH:D003643), cancer (MESH:D009369), pCR (MESH:D005598), TNBC (MESH:D064726), lymphopenia (MESH:D008231), lymph node (MESH:D000072717), nodal (MESH:D013611), infection (MESH:D007239)
- **Chemicals:** taxanes (MESH:D043823), Doxorubicin (MESH:D004317), cyclophosphamide (MESH:D003520), steroid (MESH:D013256), docetaxel (MESH:D000077143), Paclitaxel (MESH:D017239), anthracycline (MESH:D018943), taxane (MESH:C080625), NA (MESH:D012964), ALC (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12992397/full.md

## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12992397/full.md

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Source: https://tomesphere.com/paper/PMC12992397