Histopathologic and molecular profile of gliomas diagnosed in Lagos, Nigeria.

IF 2.4 Q2 CLINICAL NEUROLOGY Neuro-oncology practice Pub Date : 2024-06-22 eCollection Date: 2024-12-01 DOI:10.1093/nop/npae059
Lateef A Odukoya, Cristiane M Ida, Jeanette E Eckel-Passow, Thomas M Kollmeyer, Rachael Vaubel, Daniel H Lachance, Ekokobe Fonkem, Kabir B Badmos, Olufemi B Bankole, Henry Llewellyn, Gasper J Kitange, Kenneth Aldape, Adetola O Daramola, Charles C Anunobi, Robert B Jenkins
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Abstract

Background: The optimal diagnosis and management of patients with brain tumors currently uses the 2021 WHO integrated diagnosis of histomorphologic and molecular features. However, neuro-oncology practice in resource-limited settings usually relies solely on histomorphology. This study aimed to classify glioma cases diagnosed in the Department of Anatomic and Molecular Pathology, Lagos University Teaching Hospital, using the 2021 WHO CNS tumor classification.

Methods: Fifty-six brain tumors from 55 patients diagnosed with glioma between 2013 and 2021 were reevaluated for morphologic diagnosis. Molecular features were determined from formalin-fixed paraffin-embedded (FFPE) tissue using immunohistochemistry (IHC) for IDH1-R132H, ATRX, BRAF-V600E, p53, Ki67, and H3-K27M, OncoScan chromosomal microarray for copy number, targeted next generation sequencing for mutation and fusion and methylation array profiling.

Results: Of 55 central nervous system tumors, 3 were excluded from histomorphologic reevaluation for not being of glial or neuroepithelial origin. Of the remaining 52 patients, the median age was 20.5 years (range: 1 to 60 years), 38(73%) were males and 14(27%) were females. Seventy-one percent of the gliomas evaluated provided adequate DNA from archival FFPE tissue blocks. After applying the 2021 WHO diagnostic criteria the initial morphologic diagnosis changed for 35% (18/52) of cases. Diagnoses of 5 (9.6%) gliomas were upgraded, and 7 (14%) were downgraded.

Conclusions: This study shows that the incorporation of molecular testing can considerably improve brain tumor diagnoses in Nigeria. Furthermore, this study highlights the diagnostic challenges in resource-limited settings and what is at stake in the global disparities of brain tumor diagnosis.

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尼日利亚拉各斯确诊胶质瘤的组织病理学和分子特征。
背景:目前,脑肿瘤患者的最佳诊断和管理采用的是 2021 年世界卫生组织的组织形态学和分子特征综合诊断。然而,在资源有限的环境中,神经肿瘤学实践通常仅依赖于组织形态学。本研究旨在采用2021年世界卫生组织中枢神经系统肿瘤分类法,对拉各斯大学教学医院解剖和分子病理学系诊断的胶质瘤病例进行分类:方法:对2013年至2021年期间确诊为胶质瘤的55名患者的56个脑肿瘤进行了形态学诊断。采用免疫组化(IHC)检测IDH1-R132H、ATRX、BRAF-V600E、p53、Ki67和H3-K27M,OncoScan染色体微阵列检测拷贝数,新一代测序检测突变和融合,以及甲基化阵列分析,确定福尔马林固定石蜡包埋(FFPE)组织的分子特征:在55例中枢神经系统肿瘤中,有3例因不属于神经胶质或神经上皮起源而被排除在组织形态学再评估之外。在其余52名患者中,中位年龄为20.5岁(1至60岁),男性38人(占73%),女性14人(占27%)。在接受评估的胶质瘤中,71%能从存档的FFPE组织块中提供足够的DNA。在应用2021年世界卫生组织诊断标准后,35%的病例(18/52)的最初形态诊断发生了改变。5例(9.6%)胶质瘤的诊断升级,7例(14%)降级:这项研究表明,在尼日利亚采用分子检测可大大提高脑肿瘤的诊断率。此外,这项研究还强调了在资源有限的环境中诊断所面临的挑战,以及全球脑肿瘤诊断差异的利害关系。
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来源期刊
Neuro-oncology practice
Neuro-oncology practice CLINICAL NEUROLOGY-
CiteScore
5.30
自引率
11.10%
发文量
92
期刊介绍: Neuro-Oncology Practice focuses on the clinical aspects of the subspecialty for practicing clinicians and healthcare specialists from a variety of disciplines including physicians, nurses, physical/occupational therapists, neuropsychologists, and palliative care specialists, who have focused their careers on clinical patient care and who want to apply the latest treatment advances to their practice. These include: Applying new trial results to improve standards of patient care Translating scientific advances such as tumor molecular profiling and advanced imaging into clinical treatment decision making and personalized brain tumor therapies Raising awareness of basic, translational and clinical research in areas of symptom management, survivorship, neurocognitive function, end of life issues and caregiving
期刊最新文献
Foreword. Role of the tumor board when prescribing mutant isocitrate dehydrogenase inhibitors to patients with isocitrate dehydrogenase-mutant glioma. Financial challenges of being on long-term, high-cost medications. How do I prescribe and manage mIDH inhibitors in patients with IDH-mutant glioma? Vorasidenib: Patient and caregiver information sheet.
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