Tumoral PD-L1 Expression as a Prognostic Marker in Invasive Cervical Cancer
Carolin Schröder1, Maryam Qureischi2, Thomas Hecking3
1Department of Gynaecology and Gynaecological Oncology, University Hospital Bonn, Bonn, Germany; carolin.schroeder@ukbonn.de.
Anticancer Research
|July 29, 2026
Summary
Programmed death-ligand 1 (PD-L1) expression, measured by Combined Positive Score (CPS), is a favorable prognostic indicator for overall survival in cervical cancer (CC). Tumor Proportion Score (TPS) assessment of PD-L1 did not show prognostic significance.
Area of Science:
- Oncology
- Immunology
- Pathology
Background:
- Cervical cancer (CC) is a significant global health challenge, particularly in low-resource settings.
- Programmed death-ligand 1 (PD-L1) is an immune biomarker with potential prognostic value in various cancers.
- The prognostic role of PD-L1 in CC requires further investigation.
Purpose of the Study:
- To evaluate the clinicopathological significance of tumoral PD-L1 expression in cervical cancer.
- To determine the prognostic impact of PD-L1, assessed by Tumor Proportion Score (TPS) and Combined Positive Score (CPS), on patient outcomes in CC.
Main Methods:
- Retrospective analysis of 113 invasive CC patients treated between 2002 and 2016.
- Immunohistochemical analysis of PD-L1 (TPS and CPS), p16, p53, Ki-67, and hormone receptors on tissue microarrays.
- Correlation of PD-L1 expression with clinicopathological parameters and survival outcomes (OS, PFS).
Main Results:
- PD-L1 positivity was observed in 15.9% (TPS) and 54.9% (CPS) of CC cases.
- PD-L1 expression did not significantly correlate with most clinicopathological parameters.
- Multivariate analysis revealed PD-L1 positivity by CPS as an independent predictor of improved overall survival (OS), while TPS did not show significance.
Conclusions:
- Tumoral PD-L1 expression assessed by CPS is a favorable prognostic factor for OS in cervical cancer.
- PD-L1 assessment using TPS lacks prognostic impact in CC.
- CPS scoring offers superior insight into PD-L1-related immune activity and prognosis in CC.

