侵袭性乳腺癌的临床病理特征与pdl-1免疫组化表达的关系

Daniel Kristian Prawira Lesmana, Denny Rifsal Siregar, Dedy Hermansyah
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摘要

背景:肿瘤免疫治疗研究需要能够预测抗pd -1/PD-L1治疗临床反应的免疫生物学标志物。在接受PD-1/PD-L1通路抑制剂治疗的各种类型癌症患者中,高PD-L1表达与临床反应增加相关。研究者希望通过PD-L1的免疫组织化学表达来了解浸润性乳腺癌的临床病理特征。方法:本研究采用横断面、回顾性研究方法,对哈吉亚当马利克医院肿瘤科外科2019年1月1日至2021年12月31日的病历资料进行二次资料分析。结果:PD-L1免疫组化表达在浸润性乳腺癌中为阳性,在浸润性乳腺癌中为阴性,阳性率为76.6%,阴性率为23.3%。PD-L1的免疫组化表达在非特异性IBCs中呈阳性,在乳腺癌的每个分子亚组中都占主导地位。讨论:肿瘤可通过组成型或癌基因诱导的PD-L1表达的遗传机制、在T细胞中诱导的PD-L1表达、PD-L1缺失等几种具有不同功能意义的生物学过程显示PD-L1的阳性或阴性表达。由于缺乏T细胞和遗传事件,尽管T细胞浸润,PD-L1的表达仍被阻断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CLINICOPATHOLOGICAL CHARACTERISTICS OF INVASIVE BREAST CARCINOMA ON PDL-1 IMMUNOHISTOCHEMICAL EXPRESSION IN H. ADAM MALIK HOSPITAL MEDAN
Abstract Background: Immune biologic markers that can predict clinical response to anti-PD-1/PD-L1 therapy are needed to identify and validate tumor immunotherapy studies. High PD-L1 expression is associated with increased clinical response in patients with various types of cancer treated with inhibitors of the PD-1/PD-L1 pathway. The researcher wanted to see the clinicopathological characteristics of invasive breast carcinoma according to the immunohistochemical expression of PD-L1. Methods: This study is a descriptive study with a cross-sectional, retrospective approach by looking at secondary data from the medical records of the Department of Surgery, Oncology Division, Haji Adam Malik Hospital from January 1, 2019, to December 31, 2021. Results: Immunohistochemical expression of PD-L1 was positive in 76.6% of invasive breast carcinomas and negative in 23.3% of invasive breast carcinomas. Immunohistochemical expression of PD-L1 was positive in non-specific IBCs that predominated in every molecular subgroup of breast carcinoma. Discussion: Tumours can show positive or negative PD-L1 expression through several biological processes with different functional significance, namely the genetic mechanism of constitutive or oncogene-induced PD-L1 expression, PD-L1 expression induced in T cells, and absence of PD-L1 expression. Due to the absence of T cells and genetic events that block the expression of PD-L1 despite T cell infiltration.
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