# Prognostic value and early response stratification of a multi-biomarker panel in cervical cancer patients undergoing chemoradiotherapy

**Authors:** Yu Wang, Na Gan, Shan Ning, Yinting Qiu

PMC · DOI: 10.3389/fonc.2025.1686716 · Frontiers in Oncology · 2025-10-30

## TL;DR

A multi-biomarker panel helps predict early treatment response and survival in cervical cancer patients undergoing chemoradiotherapy.

## Contribution

The study introduces a multi-biomarker panel for early response stratification and prognosis in cervical cancer.

## Key findings

- Elevated SCC-Ag, CA125, IL-6, CRP, and high NLR/PLR correlate with advanced disease and poorer treatment response.
- High-risk patients had significantly lower progression-free and overall survival rates.
- The biomarker panel shows superior discrimination for early response and survival prediction.

## Abstract

Despite progress in chemoradiotherapy (CRT), outcomes in cervical cancer still vary widely. Minimally invasive biomarkers may enable risk stratification and treatment optimization.

We prospectively enrolled 164 International Federation of Gynecology and Obstetrics (FIGO) IB–IVA patients, all receiving CRT plus brachytherapy. Baseline blood markers and HPV subtypes were assessed. Treatment response was evaluated at three months, and progression-free (PFS) and overall survival (OS) were measured over a median of 36 months.

Elevated squamous cell carcinoma antigen (SCC-Ag), Cancer antigen 125 (CA125), Interleukin-6 (IL-6), C-reactive protein (CRP), and high neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio (NLR/PLR) correlated with advanced disease. At three months, 87.1% showed complete response (CR) or partial response (PR). Higher IL-6, CRP, SCC-Ag, CA125, and NLR/PLR were linked to poorer response. At 36 months, PFS and OS were 65.2% and 74.5%, respectively. High-risk patients had lower PFS (58.1% vs. 72.4%) and OS (64.5% vs. 82.0%), independent of stage, with no increase in severe toxicity.

A multi-biomarker panel shows superior discrimination for early response and is prognostic for survival in locally advanced cervical cancer. Larger, multi-institutional studies are warranted to validate this panel, standardize assays, and investigate additional markers or imaging-based strategies, ultimately facilitating more personalized therapy and improved outcomes. shows superior discrimination for early response and is prognostic for survival in locally advanced cervical cancer.

## Linked entities

- **Proteins:** MUC16 (mucin 16, cell surface associated), IL6 (interleukin 6), CRP (C-reactive protein)
- **Diseases:** cervical cancer (MONDO:0002974)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, MUC16 (mucin 16, cell surface associated) [NCBI Gene 94025] {aka CA125}
- **Diseases:** cervical cancer (MESH:D002583), toxicity (MESH:D064420)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12611648/full.md

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Source: https://tomesphere.com/paper/PMC12611648