Abstract

BackgroundAn improved risk assessment of patients with bladder cancer (BC) is important to optimize clinical management. ObjectiveTo identify whether immune cell subpopulations and cancer cell-intrinsic features are associated with outcome and response to first-line chemotherapy in BC. Design, setting, and participantsPrimary tumor tissue from 785 patients with BC (stage Ta-T4b) were stained using multiplex immunofluorescence (CD3, CD8, FOXP3, CD20, CD68, CD163, and MHC-I) and immunohistochemistry (pancytokeratin, CK5/6, GATA3, programmed death 1 [PD-1], and programmed death ligand 1 [PD-L1]). A digital image analysis quantified staining results within the carcinoma cell and stromal part of the tumor. Outcome measurements and statistical analysisPrimary endpoints were progression-free survival, recurrence-free survival, and response to first-line chemotherapy. Optimal cutoff values for investigated markers were estimated using maximally selected rank statistics and receiver operating characteristic for each primary endpoint. Time-to-event analyses were performed using Cox regression analyses. Results and limitationsSeveral immune subpopulations were independently associated with clinical outcomes. Especially, high PD-1 and PD-L1 expression was independently associated with an increased risk of recurrence and progression in non–muscle-invasive tumors, but with a lower risk of recurrence in muscle-invasive tumors. Furthermore, we observed a lower likelihood of response to first-line chemotherapy in patients with basal differentiation features. Finally, a model combining clinical risk factors with our most evident prognosticator improved prediction accuracy compared with clinical risk factors alone for progression in non–muscle-invasive BC and recurrence in muscle-invasive BC. The use of tissue microarrays and a long inclusion period are limitations to this study. ConclusionsImmune cell subpopulations and cancer cell-intrinsic features are associated with different clinical outcomes in BC. Patient summaryImmune cells play an important role in cancer development and treatment outcomes. Infiltration with specific immune cells and the presence of markers associated with immune evasion in the tumor predict clinical outcomes in bladder cancer.

Highlights

  • Bladder cancer (BC) is a highly molecularly heterogeneous disease [1], and the phenotype of each cancer cell is influenced by a multitude of cancer cell-intrinsic and cellextrinsic features, which may drive disease development and treatment resistance [2].BC is characterized by a high tumor mutational burden (TMB), and a higher TMB has been associated with an increased T-cell influx in different cancer types [3,4]

  • A high level of cytotoxic T lymphocyte (CTL) infiltration has generally been associated with a favorable prognosis in BC [7,14,15]; it has been associated with an increased risk of recurrence in non–muscle-invasive bladder cancer (NMIBC) [16]

  • A total of 785 patients were included in this retrospective study: 220 with NMIBC, 441 with localized muscle-invasive bladder cancer (MIBC), and 124 with advanced BC (T4b, N+, or M+)

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Summary

Introduction

Bladder cancer (BC) is a highly molecularly heterogeneous disease [1], and the phenotype of each cancer cell is influenced by a multitude of cancer cell-intrinsic and cellextrinsic features, which may drive disease development and treatment resistance [2].BC is characterized by a high tumor mutational burden (TMB), and a higher TMB has been associated with an increased T-cell influx in different cancer types [3,4]. Larger studies are needed to obtain consistent reliable results in order to determine optimal predictors of tumor recurrence, progression, and treatment response. We use a digital image analysis to investigate the spatial dynamics of cancer cell-intrinsic and cell-extrinsic features during disease development and their impact on clinical outcomes. Objective: To identify whether immune cell subpopulations and cancer cell-intrinsic features are associated with outcome and response to first-line chemotherapy in BC. Outcome measurements and statistical analysis: Primary endpoints were progressionfree survival, recurrence-free survival, and response to first-line chemotherapy. High PD-1 and PD-L1 expression was independently associated with an increased risk of recurrence and progression in non–muscleinvasive tumors, but with a lower risk of recurrence in muscle-invasive tumors.

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