Pd-l1 expression in muscle invasive urothelial carcinomas as assessed via immunohistochemistry: Correlations with specific clinical and pathological features, with emphasis on prognosis after radical cystectomy

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Abstract

In the present study, we analyzed Programmed Death Ligand-1 (PD-L1) expression in radical cystectomy (RC) specimens from patients with muscle-invasive urothelial carcinoma (UC), in order to assess any correlations with specific clinicopathological features and its potential prognostic value. A multi-institutional study was performed within the departments of urology and pathology at the Mureș County Hospital, Romania, and Centre Hospitalier Lyon Sud, France. Sixty-nine patients with MIBC were included, for whom tumor histology (conventional versus histological variant/differentiation), tumor extension (T), lymph node involvement (N), and distant metastases (M) were recorded. PD-L1 immunostaining was performed using the 22C3 clone and was interpreted using the combined positive score (CPS) as recommended (Dako Agilent, Santa Clara, CA, USA). Positive PD-L1 immunostaining was more prevalent among UCs with squamous differentiation compared to conventional UCs and trended towards an improved OS (p = 0.366). We found the T stage to be a risk factor for poor survival in PD-L1-positive patients (HR 2.9, p = 0.021), along with the N stage in PD-L1-negative patients (HR 1.98, p = 0.007). No other clinicopathological factor was found to be significantly associated with PD-L1 positivity. Thus, we confirm the need for PD-L1 immunostaining prior to initiating immune checkpoint inhibitor therapy for a more accurate assessment of the patients’ chances of responding to treatment.

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Nechifor-Boilă, I. A., Loghin, A., Nechifor-Boilă, A., Decaussin-Petrucci, M., Voidăzan, S., Chibelean, B. C., … Borda, A. (2021). Pd-l1 expression in muscle invasive urothelial carcinomas as assessed via immunohistochemistry: Correlations with specific clinical and pathological features, with emphasis on prognosis after radical cystectomy. Life, 11(5). https://doi.org/10.3390/life11050404

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