基于印度尼西亚万隆主要三级转诊医院的临床和组织病理学发现,胶质母细胞瘤的患病率-未另行说明(NOS

H. Bolly, A. Faried, Danny Halim, Y. Hermanto, F. P. Tjahjono, M. Arifin
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引用次数: 0

摘要

胶质母细胞瘤是成人中最致命的恶性脑肿瘤。胶质母细胞瘤化疗耐药、预后差、生存率低是目前治疗胶质母细胞瘤的主要挑战。世界卫生组织(WHO) 2016年分类通过异柠檬酸脱氢酶(IDH)的突变状态确定了两种类型的胶质母细胞瘤;由于我国的国民保险预算有限,我们不能在我国的机构中自由地应用它。我们的目的是根据其临床表现和组织病理学发现发现胶质母细胞瘤-非特异性(NOS)的患病率和预后。方法:根据2012-2017年48例胶质母细胞瘤- nos患者的临床和组织学结果进行逆行分析。我们分析了其特点、主诉、病变部位、宏观表现、治疗和最终结果。结果:胶质母细胞瘤- nos是最常见的胶质瘤类型,多发生于49.29±12.13岁(17-72岁)的成年人。肿瘤主要累及额叶(25%),主诉为慢性进行性头痛(90%);93.8%的患者术后经组织病理检查行肿瘤切除及放化疗。中位生存期为18个月,三级转诊医院胶质母细胞瘤- nos患病率为4.72%。结论:希望我们的研究能够提高对胶质母细胞瘤- nos患病率的地区差异的认识,并为确定区域危险因素铺平道路,从而使我们能够完善胶质母细胞瘤的检测、预防和管理方案。为了实现个性化医疗,需要进一步的研究,将分子技术结合到IDH1突变型或野生型患者的肿瘤分析中。
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Prevalence of Glioblastoma-Not Otherwise Specified (NOS) Based on the Clinical and Histopathology Findings in Main Tertiary Referral Hospital in Bandung, Indonesia
Introduction: Glioblastoma is the deadliest malignant brain tumors in adults. The main challenges in treating glioblastoma are its resistance to the chemo-radiotherapy, poor outcome and low survival rate. The World Health Organization (WHO) 2016 classification identifies two types of glioblastoma by its mutational status of isocitrate dehydrogenase (IDH); since our national insurance experiences budget-limitation, we could not freely apply it in our institutions. We aims to find the prevalence and outcome of glioblastoma-not otherwise specified (NOS) based on its clinical manifestations and histopathology findings. Methods: We performed retrograde-analysis based on clinical and histology findings on 48 glioblastoma-NOS patients from 2012-2017. We analyzed its characteristic, primary complains, lesions location, macroscopic findings, therapy and the final outcomes. Results: Glioblastoma-NOS is the most common type of gliomas occurs in adults ages 49.29±12.13 years (range 17-72 years). The tumor predominantly involves the frontal lobe (25%) with chronic progressive headache as the chief complaint (90%); 93.8% of the patients underwent tumor removal and received chemo-radiotherapy after surgery based on the histopathology findings. The median survival is 18 months and the prevalence of glioblastoma-NOS in our tertiary referral hospital is 4.72%. Conclusion: Hopefully, our study will improve the understanding of the regional differences in glioblastoma-NOS prevalence and pave the way for identifying the regional risk factors that would allow us to improve the protocols on glioblastoma detection, prevention and management. Further studies, incorporating molecular techniques into a patient’s tumor analysis for IDH1 mutant or wild type are required for the promise of personalized medicine.
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