DOI: 10.4103/ijpm.ijpm_16_26 ISSN: 0377-4929

PD-L1 Expression in muscle-invasive bladder carcinoma: correlation with tumor–stroma ratio and clinicopathological parameters

Anubhuti Chaturvedi, Irfana Nisam, Varuna Mallya, Shramana Mandal, Chandra Bhushan Singh

ABSTRACT

Background:

Muscle-invasive bladder carcinoma (MIBC) is an aggressive malignancy with significant morbidity and mortality. The recent incorporation of immune checkpoint inhibitors targeting the PD-1/PD-L1 axis has increased interest in immunohistochemical biomarkers. Tumor–stroma ratio (TSR) has also emerged as a potential prognostic marker reflecting the tumor microenvironment. This study evaluated programmed death-ligand 1 (PD-L1) expression and TSR in MIBC and analyzed their association with clinicopathological parameters.

Materials and Methods:

This retrospective study included 58 cases of biopsy-proven MIBC (pT2 and above) diagnosed over an 8-year period. Histopathological evaluation was performed according to WHO 2022 and AJCC 8 th edition criteria. PD-L1 immunohistochemistry was carried out using a rabbit monoclonal antibody and interpreted using the combined positive score (CPS), with CPS ≥ 10 considered positive. TSR was assessed histologically using a 50% cutoff. Associations were analyzed using the Chi-square test, with P < 0.05 considered significant.

Results:

The cohort demonstrated a male predominance (86.2%) with a mean age of 58.4 ± 10.2 years. PD-L1 expression was observed in 44.8% of cases and showed a significant association with higher WHO/ISUP tumor grade ( P = 0.01), but not with age, gender, tumor stage, lymphovascular invasion, perineural invasion, lymph node status, or TSR. TSR showed a statistically significant association with pathological T stage ( P = 0.04), with higher stromal content seen in advanced tumors.

Conclusions:

PD-L1 expression in MIBC correlates with higher tumor grade, whereas tumor–stroma ratio (TSR) is associated with advanced pathological T stage. These findings support the potential role of tumor microenvironment–based markers in pathological stratification of MIBC and warrant further prospective validation.

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