Abstract

BackgroundAdrenocortical carcinoma (ACC) is a rare tumor in which prognostic factors are still not well established. Programmed Death Ligand-1 (PD-L1) expression in ACC and its association with clinico-pathological features and survival outcomes are unknown.MethodsFormalin-fixed paraffin-embedded (FFPE) specimens were obtained from 28 patients with ACC. PD-L1 expression was evaluated by immunohistochemistry (IHC) in both tumor cell membrane and tumor infiltrating mononuclear cells (TIMC). PD-L1 positivity on tumor cells was defined as ≥5% tumor cell membrane staining. TIMC were evaluated by IHC using a CD45 monoclonal antibody. For PD-L1 expression in TIMC, a combined score based on the extent of infiltrates and percentage of positive cells was developed. Any score greater that zero was considered PD-L1 positive. Baseline clinico-pathological characteristics and follow up data were retrospectively collected. Comparisons between PD-L1 expression and clinico-pathological features were evaluated using unpaired t-test and Fisher’s exact test. Kaplan-Meier method and log-rank test were used to assess association between PD-L1 expression and 5-year overall survival (OS).ResultsAmong 28 patients with surgically treated ACC, 3 (10.7%) were considered PD-L1 positive on tumor cell membrane. On the other hand, PD-L1 expression in TIMC was performed in 27 specimens and PD-L1 positive staining was observed in 19 (70.4%) patients. PD-L1 positivity in either tumor cell membrane or TIMC was not significantly associated with higher stage at diagnosis, higher tumor grade, excessive hormone secretion, or OS.ConclusionsPD-L1 expression can exist in ACC in both tumor cell membrane and TIMC with no relationship to clinico-pathologic parameters or survival.Electronic supplementary materialThe online version of this article (doi:10.1186/s40425-015-0047-3) contains supplementary material, which is available to authorized users.

Highlights

  • Adrenocortical carcinoma (ACC) is a rare tumor in which prognostic factors are still not well established

  • Patients and tumor characteristics A total of 28 patients with ACC were included in this study

  • The stage at diagnosis was defined pathologically according to International Union Against Cancer (UICC) and European Network for the Study of Adrenal Tumors (ENSAT) staging systems [23]

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Summary

Introduction

Adrenocortical carcinoma (ACC) is a rare tumor in which prognostic factors are still not well established. Adrenocortical carcinoma (ACC) is a rare and highly lethal malignancy arising from the adrenal cortex. ACC carries a poor prognosis with the most consistent prognostic factor being tumor stage at the time of diagnosis [3]. Retrospective studies have reported a 5year survival rate of 24% for stage III and 0% for stage IV disease [4]. Complete surgical resection remains the only chance of cure for patients with early-stage disease (stage I and II). Resection is the mainstay of therapy, even for patients with locally advanced disease. Despite aggressive management, close to 80% of surgically treated patients will develop subsequent metastatic disease [6]

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