Correlation of PD-L1 expression with different clinico-pathological and immunohistochemical features of ovarian surface epithelial tumors.

IF 2.8 3区 医学 Q2 ONCOLOGY
Clinical & Translational Oncology Pub Date : 2025-02-01 Epub Date: 2024-08-01 DOI:10.1007/s12094-024-03613-2
Asem Shalaby, Ola Shalaby, Hazem Abdullah, Mohamed Rachid Boulassel, Mohammad Arafa
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引用次数: 0

Abstract

Background: Primary carcinoma of the ovary (OCs) are responsible for a significant number of deaths related to cancer, and have the highest rate of death related to cancers of the female reproductive organs. Programmed cell death 1 (PD1) protein, acts as an immune checkpoint, and has an important role in the down-regulation of the immune system by preventing the activation of T-cells, which will weaken the autoimmunity and increases self-tolerance. This study aimed at the evaluation of the immunohistochemical (IHC) expression of PD-L1 in various primary surface ovarian epithelial tumours and to test its correlation with different clinicopathological parameters together with the expression of a panel of P53, ER and PR.

Methods: A set of 102 cases of primary ovarian surface epithelial neoplasms (benign, borderline and malignant) were collected to construct Tissue Microarray (TMA) using 3 tissue cores from each case. IHC for PD-L1, p53, PR and ER was performed. The expression of PD-L1 was evaluated in relation to some clinicopathological parameters and to the expression patterns of other markers.

Results: Expression of PD-L1 was detected in about 51% (n = 36) of malignant tumours. The malignant group significantly showed PD-L1 positivity compared to borderline and benign groups. The malignant tumours significantly showed PD-L1 and total p53 positivity in comparison to borderline group. Also, malignant tumours significantly showed higher combined positivity of PD-L1 and either PR or ER compared to borderline and benign lesions. No significant correlation was appreciated between PD-L1 expression and with any of the studied clinicopathological parameters.

Conclusions: This study showed a significant PD-L1 expression in malignant primary surface epithelial tumours. Construction of a panel of IHC markers, including PD-L1, could have a potential value to define patients those would benefit from the addition of immunotherapy to the treatment plan.

Abstract Image

PD-L1 表达与卵巢表面上皮肿瘤不同临床病理和免疫组化特征的相关性。
背景:原发性卵巢癌(OCs)是造成大量癌症死亡的原因,也是女性生殖器官癌症中死亡率最高的一种。程序性细胞死亡 1(PD1)蛋白作为一种免疫检查点,通过阻止 T 细胞的活化,在免疫系统的下调过程中发挥着重要作用,这将削弱自身免疫力并增加自我耐受性。本研究旨在评估 PD-L1 在各种原发性表面卵巢上皮肿瘤中的免疫组化(IHC)表达,并检测其与不同临床病理参数以及 P53、ER 和 PR 面板表达的相关性:方法:收集102例原发性卵巢表面上皮肿瘤(良性、边缘性和恶性),用每个病例的3个组织核构建组织芯片(TMA)。对 PD-L1、p53、PR 和 ER 进行了 IHC 检测。评估了 PD-L1 的表达与一些临床病理参数以及其他标记物表达模式的关系:结果:约51%的恶性肿瘤(n = 36)检测到PD-L1的表达。与边缘组和良性组相比,恶性组明显显示出 PD-L1 阳性。与边缘组相比,恶性肿瘤明显显示出 PD-L1 和总 p53 阳性。此外,与边缘和良性病变相比,恶性肿瘤的PD-L1和PR或ER合并阳性率明显更高。PD-L1的表达与所研究的临床病理参数之间没有明显的相关性:结论:本研究表明,PD-L1在恶性原发性表面上皮肿瘤中有明显表达。建立包括 PD-L1 在内的 IHC 标志物小组可能具有潜在价值,可用于确定哪些患者可从治疗计划中增加的免疫疗法中获益。
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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
240
审稿时长
1 months
期刊介绍: Clinical and Translational Oncology is an international journal devoted to fostering interaction between experimental and clinical oncology. It covers all aspects of research on cancer, from the more basic discoveries dealing with both cell and molecular biology of tumour cells, to the most advanced clinical assays of conventional and new drugs. In addition, the journal has a strong commitment to facilitating the transfer of knowledge from the basic laboratory to the clinical practice, with the publication of educational series devoted to closing the gap between molecular and clinical oncologists. Molecular biology of tumours, identification of new targets for cancer therapy, and new technologies for research and treatment of cancer are the major themes covered by the educational series. Full research articles on a broad spectrum of subjects, including the molecular and cellular bases of disease, aetiology, pathophysiology, pathology, epidemiology, clinical features, and the diagnosis, prognosis and treatment of cancer, will be considered for publication.
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