Molecular Classification of Gastric Cancer With Emphasis on PDL-1 Expression: The First Report From Iran

IF 1.9 Q3 PATHOLOGY
F. Amirmoezi, B. Geramizadeh
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引用次数: 1

Abstract

Background: Gastric cancer is one of the lethal cancers and there is no effective treatment for these patients and still, 5-year survival rate is about 25% to 30%. Finding reliable biomarkers for early-stage diagnosis, targeted therapy, and survival prediction is a priority in this cancer. Objectives: In this study we were trying to know about the molecular classification of gastric cancers in a group of patients from the South of Iran. Patients and Methods: In a cross sectional study, 50 specimens of gastric cancer were selected that have enough tissue to be stained by immunohistochemistry (IHC). IHC was performed for Her-2, mismatch repair genes (MLH-1, MSH-2, MSH-6, and PMS-2), and PDL-1. Frequency of positive makers was compared with survival and outcome. Results and Conclusion: In our study, deficient MMR (dMMR) was detected in 4 patients (8.0%). PD-L1 expression in tumor cells (TC) was observed in 1 of 4 cases (25%) with PMS2 loss. However, PD-L1 in TCs and TILs (tumor infiltrating lymphocytes) was negative in 1 case with MLH1 loss and in 3 of 4 cases with PMS2 loss, which was not statistically significant. All of our 50 cases were positive for MSH2 and MSH6, 24% of which showed TCs with PDL-1 expression and 32% of them in TIL. HER2 was positive in 2 (2/50, 4.0%) cases, among which all of the cases were positive for PD-L1 expression in TCs and TILs, respectively. However, in HER2-negative group, 26.2% (11/42) and 28.6% (12/42) of tumors were positive for PD-L1 in TCs and TILs, respectively. The expression rate of PD-L1 in HER2 negative TCs was significantly higher than that in HER2 positive TCs (P = .033). Immunohistochemistry for Her-2 was equivocal in 6 cases (12.0%) none of which expressed PD-L1 in tumor cells. In our study minimum and maximum survival times from detection of gastric cancer were 1 and 87 months, respectively. The mean ± SD and median ± SD of overall survival time were 30.69 ± 4.88 and 18 ± 1.45 months, respectively. One and 3-year survival rates of 40% and 24%, respectively. PD-L1 expression was not associated with survival, but its expression was associated with intestinal type Lauren classification and negative HER-2. PD-L1 positivity in tumor cells or tumor infiltrating lymphocytes was not an independent prognostic factor in gastric cancer.
以PDL-1表达为重点的癌症分子分类:伊朗首次报道
背景:癌症是恶性肿瘤之一,目前尚无有效的治疗方法,5年生存率约为25%-30%。寻找用于早期诊断、靶向治疗和生存预测的可靠生物标志物是这种癌症的优先事项。目的:在这项研究中,我们试图了解来自伊朗南部的一组患者胃癌的分子分类。患者和方法:在一项横断面研究中,选择50例癌症标本,这些标本具有足够的组织进行免疫组织化学(IHC)染色。对Her-2、错配修复基因(MLH-1、MSH-2、MSH-6和PMS-2)和PDL-1进行IHC。将阳性标记的频率与生存率和结果进行比较。结果与结论:在我们的研究中,4例(8.0%)患者检测到MMR缺陷,4例PMS2缺失患者中有1例(25%)肿瘤细胞中PD-L1表达。然而,在MLH1缺失的1例和PMS2缺失的4例中,TC和TIL(肿瘤浸润淋巴细胞)中的PD-L1为阴性,这在统计学上没有显著性。在我们的50例病例中,MSH2和MSH6均呈阳性,其中24%的TCs表达PDL-1,32%的TCs在TIL中表达。HER2阳性2例(2/50,4.0%),其中所有病例分别在TC和TIL中表达PD-L1。然而,在HER2阴性组中,TCs和TIL中分别有26.2%(11/42)和28.6%(12/42)的肿瘤PD-L1阳性。PD-L1在HER2阴性TC中的表达率显著高于HER2阳性TC(P=0.033)。Her-2的免疫组化在6例(12.0%)中不明确,其中没有一例在肿瘤细胞中表达PD-L1。在我们的研究中,癌症检测的最小和最大存活时间分别为1个月和87个月。总生存时间的平均值±SD和中位数±SD分别为30.69±4.88和18±1.45个月。一年和三年生存率分别为40%和24%。PD-L1的表达与生存率无关,但其表达与肠型Lauren分类和阴性HER-2有关。肿瘤细胞或肿瘤浸润性淋巴细胞中PD-L1阳性不是癌症的独立预后因素。
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来源期刊
Clinical Pathology
Clinical Pathology PATHOLOGY-
CiteScore
2.20
自引率
7.70%
发文量
66
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