Bim Expression in Peritumoral Lymphocytes is Associated with Survival in Patients with Metastatic Clear Cell Renal Cell Carcinoma

Author:

Bhindi Bimal12,Bearrick Elizabeth N.1,Cheville John C.3,Lohse Christine M.4,Mason Ross J.15,Shah Paras1,Harrington Susan1,Zhang Henan1,Dong Haidong1,Boorjian Stephen A.1,Thompson R. Houston1,Leibovich Bradley C.1

Affiliation:

1. Department of Urology, Mayo Clinic, Rochester, MN, USA

2. Southern Alberta Institute of Urology, Calgary, AB, Canada

3. Department of Pathology, Mayo Clinic, Rochester, MN, USA

4. Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA

5. Department of Urology, Dalhousie University, Halifax, NS, Canada

Abstract

BACKGROUND: Bim (BCL-2-interacting mediator of cell death) is a downstream pro-apoptotic signaling molecule activated by the PD-1 pathway. OBJECTIVE: We sought to determine if Bim expression in peritumoral T-lymphocytes (PTLs) is associated with survival in patients with metastatic clear cell renal cell carcinoma (ccRCC). METHODS: Immunohistochemistry staining for Bim was performed on paraffin-embedded tumor tissue blocks from patients with metastatic ccRCC who underwent nephrectomy between 1990-2004. Associations of Bim expression with cancer-specific survival (CSS) and overall survival (OS) from date of metastasis were evaluated using multivariable Cox regression models, adjusting for age, sex, and metastases-score. RESULTS: 525 patients with metastatic ccRCC, of whom 169 (32%) had metastases at time of nephrectomy were studied. After multivariable adjustment, high Bim expression remained associated with worse CSS (HR = 1.31; 95% CI 1.07–1.59; p = 0.008) and OS (HR = 1.28; 95% CI 1.06–1.55; p = 0.01). The interaction between Bim and PD-L1 was not statistically significant for CSS (p = 0.68) or OS (p = 0.57), suggesting that the associations between Bim and survival outcomes were not significantly different based on tumor PD-L1 expression. CONCLUSION: High Bim expression in PTLs at nephrectomy is prognostic of worse CSS and OS in patients with metastatic ccRCC, irrespective of tumor PD-L1 expression. The role of earlier PD-1/PD-L1-directed therapy warrants evaluation in these patients.

Publisher

IOS Press

Subject

Nephrology,Oncology

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