利用组织学和免疫组化对弥漫性胶质瘤进行分类的算法。

IF 1.1 Q4 ONCOLOGY International journal of clinical and experimental pathology Pub Date : 2024-01-15 eCollection Date: 2024-01-01
Chandni Bhandary Panambur, Subhashini Ramamoorthy, Bheemanathi Hanuman Srinivas, Sree Rekha Jinkala, Surendar Kumar Verma, Gopalakrishnan Madhavan Sasidharan
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引用次数: 0

摘要

简介弥漫性胶质瘤占原发性脑肿瘤的 28%。直到最近,形态学外观仍是对这些肿瘤进行分类的唯一标准。然而,WHO 2016 将分子信息纳入胶质瘤的初级诊断,如异柠檬酸脱氢酶 1(IDH1)、α地中海贫血/智力低下综合征 X 染色体(ATRX)以及 FISH 的 1p/19q 编码缺失。在资源有限且无法使用 FISH 的情况下,有人建议将 Alpha 连环素(INA)作为替代 IHC 标记:材料和方法:在病理科进行的横断面研究,为期两年。组织块、临床和放射学资料均来自科室档案。评估形态学细节后,应用常规 IHC 标记(如 GFAP、Ki67 和 P53)以及分子标记(如 IDH-1、ATRX 和 lNA):55例弥漫性胶质瘤中,23例为星形细胞瘤,32例为少突胶质细胞瘤,总平均发病年龄为(41.49 ± 12.47)岁。在我们的研究中,弥漫性胶质瘤中 IDH-1 的表达率为 89.1%。在 95.7% 的星形细胞瘤中观察到 ATRX 基因表达的改变。75%的少突胶质细胞瘤表达INA,两个级别的表达量无明显差异。根据使用分子替代标记物的算法,弥漫性胶质瘤被分为六个不同的组别。IDH突变、ATRX表达缺失的星形细胞瘤和IDH突变、INA阳性的少突胶质细胞瘤是无需进一步分子检测的两类。这两类病例占 72.7%,无需进一步检查:结论:实施表型-基因型联合诊断,并使用组织形态学和免疫组化替代物进行分子遗传学改变,将产生更加同质化和定义更窄的诊断实体,从而提供更好的预后和明确的治疗。在资源有限的情况下,这种方法还具有成本效益。
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Algorithmic approach utilizing histology and immunohistochemistry for the current classification of diffuse glioma.

Introduction: Diffuse glioma constitutes 28% of primary brain tumors. Until recently morphologic appearance was the only criterion for classifying these tumors. However, WHO 2016 incorporates molecular information in the primary diagnosis of gliomas such as Isocitrate dehydrogenase 1 (IDH1), Alpha thalassemia/mental retardation syndrome X inked (ATRX) as well as 1p/19q codeletion on FISH. In a resource-limited setup where FISH is not available, Alpha internexin (INA) has been suggested as a surrogate IHC marker.

Material and methods: Cross-sectional study conducted in the Department of Pathology for two years. Tissue blocks and clinical as well as radiological details were obtained from departmental archives. After assessing the morphologic details, routine IHC markers such as GFAP, Ki67 and P53 along with molecular markers like IDH-1, ATRX, and lNA were applied.

Results: Out of 55 cases of diffuse glioma, 23 cases of astrocytoma and 32 cases of oligodendroglioma with an overall mean age of presentation of 41.49 ± 12.47 years. IDH-1 expression among diffuse glioma was 89.1% in our study. Alteration in the ATRX gene expression was observed in 95.7% of astrocytomas. 75% of oligodendrogliomas expressed INA with no significant difference in expression between the two grades. Based on the algorithmic approach using molecular surrogate markers, diffuse gliomas were categorized into six distinct groups. IDH-mutant, ATRX loss of expression astrocytoma and IDH-mutant, INA positive oligodendroglioma are two categories that do not require further molecular testing. This comprises 72.7% of the cases and these do not warrant further workup.

Conclusion: Implementation of combined phenotypic-genotypic diagnosis with the use of histomorphology and immunohistochemical surrogates for molecular genetic alterations will yield more homogeneous and narrowly defined diagnostic entities which will provide better prognostication and definitive treatment. It also is cost-effective in a resource-limited setup.

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期刊介绍: The International Journal of Clinical and Experimental Pathology (IJCEP, ISSN 1936-2625) is a peer reviewed, open access online journal. It was founded in 2008 by an international group of academic pathologists and scientists who are devoted to the scientific exploration of human disease and the rapid dissemination of original data. Unlike most other open access online journals, IJCEP will keep all the traditional features of paper print that we are all familiar with, such as continuous volume and issue numbers, as well as continuous page numbers to keep our warm feelings towards an academic journal. Unlike most other open access online journals, IJCEP will keep all the traditional features of paper print that we are all familiar with, such as continuous volume and issue numbers, as well as continuous page numbers to keep our warm feelings towards an academic journal.
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