CD8+ Tumor-Infiltrating Lymphocyte Abundance Is a Positive Prognostic Indicator in Nasopharyngeal Cancer

Author:

Shi Wei1ORCID,Fijardo Mackenzie12ORCID,Bruce Jeff P.1ORCID,Su Jie3ORCID,Xu Wei34ORCID,Bell Rachel1ORCID,Bissey Pierre-Antoine1ORCID,Hui Angela B.Y.5ORCID,Waldron John678ORCID,Pugh Trevor J.1910ORCID,Yip Kenneth W.12ORCID,Liu Fei-Fei16789ORCID

Affiliation:

1. 1Research Institute, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.

2. 2Department of Cell and Systems Biology, University of Toronto, Toronto, Ontario, Canada.

3. 3Department of Biostatistics, Princess Margaret Cancer Centre/University Health Network, Toronto, Ontario, Canada.

4. 4Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.

5. 5Stanford University, Stanford, California.

6. 6Radiation Medicine Program, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.

7. 7Department of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada.

8. 8Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada.

9. 9Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.

10. 10Ontario Institute for Cancer Research, Toronto, Ontario, Canada.

Abstract

Abstract Purpose: Tumor-infiltrating lymphocytes (TIL) are immune cell populations found within tumors, critical in the antigen-specific host immune response. In this study, we aimed to elucidate the prognostic significance of CD3+, CD4+, and CD8+ TILs in nasopharyngeal cancer (NPC). Experimental Design: Immune cell infiltration was quantified in NPC samples (n = 50) using RNA-sequencing (RNA-seq) data based on rearranged T-cell receptor (TCR) reads and the Estimation of Stromal and Immune cells in malignant tumors using expression data (ESTIMATE) immune score tool. The differential abundances of TIL subset populations were also characterized through IHC staining of formalin-fixed, paraffin-embedded samples from a training cohort (n = 35), which was a subset of the RNA-seq cohort (n = 50). Results: In the RNA-seq cohort, patients with higher rearranged TCR reads experienced superior 5- and 10-year overall survival (OS; P < 0.001), and disease-free survival (DFS; P < 0.001). Similarly, patients with higher ESTIMATE immune scores experienced superior 5- and 10-year OS (P = 0.024) and DFS (P = 0.007). In the training cohort, high abundances of CD8+ TILs were significantly associated with improved 5- and 10-year OS (P = 0.003) and DFS (P = 0.005). These findings were corroborated in an independent validation cohort (n = 84), and combined analysis of the training and validation cohorts [n = 119 (35+84)], which further demonstrated improved 5- and 10-year survival in terms of locoregional control (P < 0.001) and distant metastasis (P = 0.03). Conclusions: Taken together, our study highlights the prognostic value of CD8+ TILs in NPC, and the potential of future investigations into cellular-based immunotherapies employing CD8+ lymphocytes.

Funder

Canadian Institutes of Health Research

Canadian Cancer Society

The Peter and Shelagh Godsoe Chair in Radiation Medicine

The University of Toronto Faculty of Medicine

Princess Margaret Cancer Centre

The Princess Margaret Cancer Foundation

The Ontario Ministry of Health

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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