Współczesna Onkologia

Baseline values and dynamic changes of inflammatory indices are not prognostic for progressionfree survival in first-line pembrolizumab plus chemotherapy for programmed death-ligand 1-positive advanced triple-negative breast cancer: a Polish multicenter cohort study

  1. Lower Silesian Comprehensive Cancer Center, Wroclaw Medical University, Wroclaw, Poland

  2. Maria Sklodowska-Curie Bialystok Oncology Center, Bialystok, Poland

  3. Department of Breast Cancer and Reconstructive Surgery, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland

  4. Breast Cancer Unit, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Gliwice, Poland

  5. Department of Clinical Oncology, Maritime Hospital in Gdynia, Gdynia, Poland

  6. West Pomeranian Oncology Center, Szczecin, Poland

  7. Department of Clinical Oncology, Ludwik Rydygier Hospital, Cracow, Poland

  8. Department of Clinical Oncology, Holy Cross Cancer Centre, Kielce, Poland

  9. Statistical Analysis Centre, Wroclaw Medical University, Wroclaw, Poland

  10. Department of Gynaecological Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, Cracow Branch, Cracow, Poland

  11. Department of Anatomy, Jagiellonian University Medical College, Cracow, Poland

  12. Department of Clinical Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, Cracow Branch, Cracow, Poland

Contemp Oncol (Pozn) 2026; 30 (3)

Online publish date: 2026/10/26
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Introduction

Peripheral blood inflammatory indices are potential biomarkers in immuno-oncology. However, their prognostic value in programmed death-ligand 1 (PD-L1)-positive metastatic triple-negative breast cancer (mTNBC) treated with first-line pembrolizumab-based chemoimmunotherapy is uncertain. We evaluated associations with progression-free survival (PFS) and immunotherapy-related adverse events (irAEs).

Material and methods

In this retrospective multicentre study, 89 women with PD-L1-positive (combined positive score ≥ 10) mTNBC treated in 13 Polish centres (September 2022 to February 2025) received pembrolizumab 200 mg q3w plus chemotherapy. Baseline and pre-cycle 2 blood counts were used to calculate systemic immune-inflammation index, systemic inflammation response index (SIRI), neutrophil-to- lymphocyte ratio, platelet-to-lymphocyte ratio and lymphocyte-to-monocyte ratio. Progression-free survival was assessed using multivariate Cox regression models without predefined cut-offs. Associations with irAEs were evaluated using non-parametric tests.

Results

In multivariable analyses, none of the baseline inflammatory indices were significantly associated with PFS (9.3 months [95% CI: 6.6–14.7]). Early on-treatment changes (baseline to pre-cycle 2) were also not significantly associated with PFS, although ΔSIRI showed a non-significant trend (p = 0.08). No significant associations were found between inflammatory indices (baseline or dynamic) and irAEs.

Conclusions

In this real-world cohort of PD-L1-positive mTNBC treated first-line with pembrolizumab plus chemotherapy, baseline and early-change inflammatory indices were not independently associated with PFS or irAEs and do not support routine clinical use in this setting.

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