Department of Zoology, Sri Venkateswara College, University of Delhi, New Delhi, India.
Department of Ocular Pathology, Dr Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, New Delhi, India.
Indian J Ophthalmol. 2019 Dec;67(12):1983-1987. doi: 10.4103/ijo.IJO_2056_18.
Eyelid sebaceous gland carcinoma (SGC) is an aggressive but rare malignancy of ocular region. Over-expression of PD-L1 and PD-1 has been demonstrated in a variety of solid tumors including conjunctival melanoma. PD-L1 is an immunoinhibitory molecule that suppresses the effective T cells response against tumor antigen leading to the progression of tumors. Inhibitors of the interaction of PD-L1 and PD-1 are associated with good clinical response various carcinomas. The prognostic value of the PD-1/PD-L1 axis in SGC remains unexplored. The purpose of this study was to evaluate expressions of PD-1 and its ligand PD-L1 in SGC and correlate its expression with clinicopathological features and patients survival.
The immunohistochemical expression of PD-L1 and PD-1 was evaluated in 30 SGC cases.
PD-L1 immunopositivity was detected in 41.9% of the SGC cases. PD-1 expression in tumor infiltrative lymphocytes (TILs) was observed in 53.3% samples. Tumor PD-L1 positivity, PD-1 expression in TILs and tumor size (>10 mm) was associated with reduced disease-free survival. On multivariate analysis only tumor size (>10 mm) and a combined positivity of PD-L1 in tumor cells and PD-1 in TILs with an odds ratio of 5.212 (95% confidence interval 1.449-18.737) continued to be significantly associated with SGC recurrence.
PD-L1 is overexpressed in 50% of SGC cases. The combined tumor PD-L1 positivity and TILs showing PD-1 expression within the same SGC patient's samples predict high-risk SGC, suggesting that the up-regulation of PD-L1 in tumor cells and PD-1 positivity within the same SGC patient may aggravate tumor recurrence.
眼睑皮脂腺癌(SGC)是一种侵袭性但罕见的眼部恶性肿瘤。在包括结膜黑色素瘤在内的多种实体肿瘤中已经证实 PD-L1 和 PD-1 的过度表达。PD-L1 是一种免疫抑制分子,可抑制针对肿瘤抗原的有效 T 细胞反应,从而导致肿瘤进展。PD-L1 和 PD-1 相互作用的抑制剂与各种癌的良好临床反应相关。PD-1/PD-L1 轴在 SGC 中的预后价值尚未得到探索。本研究旨在评估 PD-1 及其配体 PD-L1 在 SGC 中的表达,并将其表达与临床病理特征和患者生存相关联。
评估了 30 例 SGC 病例中 PD-L1 和 PD-1 的免疫组织化学表达。
SGC 病例中检测到 41.9%的 PD-L1 免疫阳性。在 53.3%的样本中观察到肿瘤浸润性淋巴细胞(TILs)中的 PD-1 表达。肿瘤 PD-L1 阳性、TILs 中的 PD-1 表达和肿瘤大小(>10mm)与无病生存率降低相关。多变量分析仅显示肿瘤大小(>10mm)和肿瘤细胞 PD-L1 阳性与 TILs 中 PD-1 表达的联合阳性与比值比为 5.212(95%置信区间为 1.449-18.737),仍然与 SGC 复发显著相关。
在 50%的 SGC 病例中过表达 PD-L1。同一 SGC 患者样本中肿瘤 PD-L1 阳性和 TILs 中 PD-1 表达的联合阳性预测高危 SGC,表明肿瘤细胞中 PD-L1 的上调和同一 SGC 患者 TILs 中的 PD-1 阳性可能加重肿瘤复发。