Abstract

BackgroundProgrammed cell death ligand 1 (PD-L1) is a predictive biomarker of the response of immunotherapy in some types of cancer. In the last years it was described its expression in breast cancer, namely in triple-negative breast cancer (TNBC) cases. In order to better understand the prognostic value of PD-L1 in breast cancer, this study analysed its expression in a series of primary tumours and respective nodal metastases.MethodsPD-L1 expression was evaluated by immunohistochemistry in a series of 52 breast cancer cases and paired lymph node metastasis and correlate with the clinicopathological features of the primary tumour. The TNBC cases were re-classified using morphological and immunohistochemistry surrogate markers and the expression of PD-L1 was correlate with the different subtypes.ResultsIt was observed that the majority of the cases with PDL-1 positive in the nodal metastasis did not express PD-L1 in the primary tumour (90.0%, 10 out of 11 cases). In addition, from the cases with a negative PD-L1 expression in the primary tumour, 23.8% expressed PD-L1 in the metastasis (10 out of 42 cases).No relationship was found between the PD-L1 expression in nodal metastasis and the clinicopathological features of the primary tumour. Finally, basal-like immunosuppressed (BLIS) TN tumours seem to be less prone to express PD-L1.ConclusionAlthough without statistical significance, there is a gain in terms of the PD-L1 expression in the nodal metastasis when compared to the primary tumour. This may have therapeutic implications on immunotherapy that blocks the PD-1/PD-L1 pathway.

Highlights

  • Programmed cell death ligand 1 (PD-L1) is a predictive biomarker of the response of immunotherapy in some types of cancer

  • No association was observed between the PD-L1 expression and breast cancer molecular subtype

  • It was observed that the majority of the cases with positive PD-L1 expression in the Triple negative (TN) primary tumour belongs to the molecular subtype TN Basal-like immune-activated (BLIA) (91.67%, 11 out of 12 cases) (Table 4)

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Summary

Introduction

Programmed cell death ligand 1 (PD-L1) is a predictive biomarker of the response of immunotherapy in some types of cancer. The TN subtype has the most aggressive clinical characteristics and there is no standard treatment for these patients (Burstein et al 2015; Matos et al 2005; Nanda and Saha 2016). This subtype can be categorized according to its molecular characteristics, namely luminal androgen receptor (LAR), mesenchymal (MES), basal-like immunosuppressed (BLIS) or basal-like immune-activated (BLIA) (Burstein et al 2015). It has been demonstrated that the TN subytpe most frequently shows intra-tumour lymphocytes and expresses the programmed cell death ligand 1 (PD-L1)

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