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A case report of atypia in angiomatous microcystic meningioma: A mimicker and masker of intratumoral metastasis in a patient with no known systemic malignancy 血管瘤性微囊型脑膜瘤非典型性1例报告:一例无系统恶性肿瘤患者肿瘤内转移的模仿者和掩蔽者
Pub Date : 2021-01-01 DOI: 10.4103/glioma.glioma_31_20
H. Tan, S. Low, C. Tan
Intratumoral metastasis is rare, and in the brain, meningiomas are the most common type of primary brain tumors to harbor metastases. We report a case of angiomatous microcystic meningioma associated with intratumoral metastatic lung adenocarcinoma in a patient with no prior history of malignancy, in which the pronounced atypia of the meningioma potentially mimics or masks the minute focus of metastatic cancer. A meticulous search for intratumoral metastasis within the meningioma is recommended if metastasis is clinically suspected. A formal ethical approval for the single case report is waived by the Institutional Review Board of National University Health System, Singapore.
瘤内转移是罕见的,在大脑中,脑膜瘤是最常见的有转移的原发性脑肿瘤类型。我们报告了一例血管瘤性微囊型脑膜瘤与瘤内转移性肺腺癌相关的病例,该患者既往无恶性病史,其中脑膜瘤的明显非典型性可能模仿或掩盖了转移性癌症的微小病灶。如果临床上怀疑有转移,建议仔细检查脑膜瘤内的肿瘤内转移。新加坡国立大学卫生系统机构审查委员会放弃对单一病例报告的正式伦理批准。
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引用次数: 0
Acute toxicity of temozolomide for the treatment of anaplastic astrocytoma: A case report 替莫唑胺治疗间变性星形细胞瘤急性毒性1例
Pub Date : 2021-01-01 DOI: 10.4103/glioma.glioma_1_21
Y. Diansari, Norman Djamaluddin, Ashita Hulwah
Temozolomide is an orally administered chemotherapeutic drug that has become a standard treatment for malignant gliomas. Severe toxicity of temozolomide is rare, especially shortly after administration. We report a 37-year-old male patient diagnosed with anaplastic astrocytoma following tumor resection. He was treated postoperatively with cranial radiation and adjuvant temozolomide 150 mg/m2 for six planned cycles. However, 3 days after finishing the first cycle of temozolomide, the patient's condition deteriorated. Laboratory results showed thrombocytopenia and lymphopenia, and chest X-ray revealed an infiltrate in the right segment of the lung, suggesting pneumonia. These conditions were thought to be caused by temozolomide. Although temozolomide is generally well tolerated by glioma patients, several adverse effects have been reported. In addition, malignancy, corticosteroids, and chemotherapy are known to increase the risk of immunosuppression. Close monitoring of patients treated with temozolomide is warranted, especially brain tumor patients, due to the risk of myelosuppression and severe infection. The work was approved by the Health Research Ethics Committee of DR Mohammad Hoesin Hospital (No. 130/kepkrsmh/2020) on December 15, 2020.
替莫唑胺是一种口服化疗药物,已成为恶性胶质瘤的标准治疗方法。替莫唑胺的严重毒性是罕见的,尤其是在给药后不久。我们报告一位37岁男性患者,肿瘤切除后被诊断为间变性星形细胞瘤。术后,他接受了颅骨放疗和替莫唑胺150 mg/m2辅助治疗,共6个计划周期。然而,在完成替莫唑胺的第一个周期后3天,患者的病情恶化。实验室结果显示血小板减少和淋巴细胞减少,胸部X光片显示右肺段有浸润,提示肺炎。这些情况被认为是由替莫唑胺引起的。尽管替莫唑胺通常对神经胶质瘤患者具有良好的耐受性,但仍有一些不良反应的报道。此外,已知恶性肿瘤、皮质类固醇和化疗会增加免疫抑制的风险。由于存在骨髓抑制和严重感染的风险,有必要密切监测接受替莫唑胺治疗的患者,尤其是脑瘤患者。这项工作于2020年12月15日获得Mohammad Hoesin医生医院健康研究伦理委员会的批准(编号130/kepkrsmh/2020)。
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引用次数: 0
Neuro-oncology during the COVID-19 pandemic COVID-19大流行期间的神经肿瘤学
Pub Date : 2021-01-01 DOI: 10.4103/glioma.glioma_3_21
M. Weller, E. Rhun, P. Roth, M. Preusser
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引用次数: 0
Perspective on the current treatment strategies for glioma 胶质瘤当前治疗策略的展望
Pub Date : 2021-01-01 DOI: 10.4103/glioma.glioma_2_21
Zhongping Chen
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引用次数: 0
Clinical value of neuronavigation combined with a fluorescent staining technique during microsurgery for treating supratentorial glioma: A case-control observational study 神经导航联合荧光染色技术在显微手术治疗幕上胶质瘤中的临床价值:一项病例对照观察研究
Pub Date : 2021-01-01 DOI: 10.4103/glioma.glioma_27_20
Fugang Yang, Cheng-shi Xu, Chao Ma, Yu-hang Zhao, Zhiqiang Li
Background and Aim: Many studies have demonstrated the value of neuronavigation guided by fluorescence staining for treating glioma patients. Here, we compared the rate of overall survival (OS) and the extent of tumor resection among patients who underwent surgery with neuronavigation and fluorescence versus conventional techniques. Materials and Methods: In this case-control observational study, data from 162 patients with supratentorial glioma who underwent surgery from January 2016 to November 2017 were retrospectively analyzed, including a neuronavigation and fluorescence treatment group (combined group, n = 53) and a conventional microsurgery group (control group, n = 109). The extent of tumor resection, World Health Organization (WHO) pathological grade, eloquent areas involved, tumor diameter, preoperative Karnofsky Performance Status score, underlying diseases, chemotherapy, hospitalization days, length of operation, intraoperative blood loss, and postoperative molecular pathological indictors were recorded. OS rates were compared using the Cox proportional hazards regression model. The study was approved by the Ethics Committee of Zhongnan Hospital of Wuhan University (approval No. 2019048). Results: The total resection rate was 60.4% in the combined group and 27.5% in the control group. Multivariate logistic regression analysis revealed that involvement of eloquent areas (odds ratio [OR] = 0.455, 95% confidence interval [CI]: 0.214–0.966, P = 0.040) and the use of the combined technique (OR = 3.634, 95% CI: 1.758–7.510, P < 0.001) were independent prognostic factors affecting total glioma resection. Eloquent areas were implicated in 79 patients. Multiple logistic regression analysis revealed that the combined technique (OR = 6.041, 95% CI: 1.705–21.403, P = 0.005) was an independent prognostic factor affecting total resection. The average follow-up period was 16.4 months. Cox regression analysis revealed that the WHO tumor grade (hazard ratio [HR] = 4.782, 95% CI: 1.620-14.119, P = 0.005), chemotherapy regimen (HR = 0.324, 95% CI: 0.181–0.579, P < 0.001), IDH mutation (HR = 0.366, 95% CI: 0.154–0.870, P = 0.023), and total resection (HR = 0.458, 95% CI: 0.248–0.846, P = 0.013) were independent factors affecting the prognosis of glioma patients. Conclusions: The use of neuronavigation with fluorescent staining appears to improve the tumor resection range and the OS rate, which is an independent factor affecting the degree of resection of supratentorial glioma. The WHO tumor grade, chemotherapy regimen, IDH mutation, and total resection were independent factors affecting the prognosis of glioma patients.
背景和目的:许多研究已经证明了荧光染色引导神经导航在治疗神经胶质瘤患者中的价值。在这里,我们比较了使用神经导航和荧光技术与传统技术进行手术的患者的总生存率(OS)和肿瘤切除程度。材料和方法:在这项病例对照观察性研究中,回顾性分析了2016年1月至2017年11月接受手术的162例幕上神经胶质瘤患者的数据,包括神经导航和荧光治疗组(联合组,n=53)和常规显微外科组(对照组,n=109)。记录肿瘤切除范围、世界卫生组织(世界卫生组织)病理分级、涉及的明显区域、肿瘤直径、术前Karnofsky表现状态评分、潜在疾病、化疗、住院天数、手术时间、术中出血量和术后分子病理指标。OS发生率采用Cox比例风险回归模型进行比较。本研究经武汉大学中南医院伦理委员会批准(批准号:2019048)。结果:联合组总切除率为60.4%,对照组为27.5%。多因素逻辑回归分析显示,有说服力区域的参与(比值比[OR]=0.455,95%置信区间[CI]:0.214-0.966,P=0.040)和联合技术的使用(OR=3.634,95%CI:1.758-7.510,P<0.001)是影响胶质瘤全切除的独立预后因素。79名患者涉及隐性区域。多元逻辑回归分析显示,联合技术(OR=6.041,95%CI:1.705-21.403,P=0.005)是影响全切除的独立预后因素。平均随访16.4个月。Cox回归分析显示,世界卫生组织肿瘤分级(危险比[HR]=4.782,95%CI:1.620-14.119,P=0.005)、化疗方案(HR=0.324,95%CI:0.181–0.579,P=0.001)、IDH突变(HR=0.366,95%CI:0.154–0.870,P=0.023)和全切除(HR=0.458,95%CI0.248–0.846,P=0.013)是影响神经胶质瘤患者预后的独立因素。结论:荧光染色神经导航可提高肿瘤切除范围和OS率,OS率是影响幕上胶质瘤切除程度的独立因素。世界卫生组织肿瘤分级、化疗方案、IDH突变和全切除是影响胶质瘤患者预后的独立因素。
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引用次数: 0
Adaptive hypofractionated radiotherapy combined with chemotherapy and anti-angiogenic therapy for residual and recurrent glioblastoma after surgery: A case report 适应性低分割放疗联合化疗和抗血管生成治疗术后残留和复发性胶质母细胞瘤1例
Pub Date : 2020-10-01 DOI: 10.4103/glioma.glioma_26_20
Yuchao Ma, J. Xiao
Glioblastoma is the most common primary brain tumor in adults. There is no standard treatment for residual or recurrent glioblastoma and the prognosis is poor. Here, we report the case of a 72-year-old woman with a glioblastoma who underwent subtotal resection, after which her tumor recurred rapidly. Adaptive hypofractionated radiotherapy combined with temozolomide and bevacizumab was administered, resulting in a long progression-free survival. The study was approved by the Ethics Committee of Cancer Hospital, Chinese Academy of Medical Sciences, China.
胶质母细胞瘤是成人最常见的原发性脑肿瘤。对于残留或复发的胶质母细胞瘤没有标准的治疗方法,预后也很差。在此,我们报告了一例72岁的胶质母细胞瘤患者,她接受了次全切除术,之后肿瘤迅速复发。给予适应性低分割放疗联合替莫唑胺和贝伐单抗,使患者长期无进展生存。本研究经中国医学科学院癌症医院伦理委员会批准。
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引用次数: 0
Re-understanding of edema zone from the nerve fiber bundles: A narrative review 从神经纤维束重新认识水肿区:叙述回顾
Pub Date : 2020-10-01 DOI: 10.4103/glioma.glioma_28_20
Yong Huang, H. Ding, Y. Zhong
Spread along nerve fiber bundles is one of the most important modes of glioma invasion; however, the current guidelines for radiotherapy target areas recommend a 1–2-cm margin in all directions from the tumor border based on pretreatment imaging findings. In this article, we analyzed the relationship between edema and nerve fiber bundles in 60 glioma patients and aimed to clarify the effect of including edema on delineation of the target volume.
沿神经纤维束扩散是胶质瘤侵袭的重要方式之一;然而,目前的放疗靶区指南建议根据预处理成像结果,从肿瘤边界向各个方向划出1 - 2厘米的边缘。在本文中,我们分析了60例胶质瘤患者的水肿与神经纤维束的关系,旨在阐明包括水肿对靶体积描绘的影响。
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引用次数: 1
Diagnostic and prognostic implications of molecular status in Chinese adults with diffuse glioma: An observational study 中国成人弥漫性胶质瘤分子状态的诊断和预后意义:一项观察性研究
Pub Date : 2020-10-01 DOI: 10.4103/glioma.glioma_21_20
Leiming Wang, Zhuo Li, Cuicui Liu, Liyan Zhang, Dandan Wang, Haijing Ge, Wei-Wei Xu, Yongjuan Fu, Yanning Cai, D. Lu, Y. Piao
Background and Aim: Mutations in isocitrate dehydrogenase (IDH), co-deletion of 1p and 19q, loss or expression of the transcription regulator ATRX, and mutations in telomerase reverse transcriptase (TERT) gene promoters are intimately linked with diffuse gliomas. We further explored the roles of the key molecules in adulthood diffuse gliomas and their prognosis. Materials and Methods: A total of 413 patients who underwent primary surgery between 2009 and 2015 at Xuanwu Hospital, Beijing, China, were included in this observational study. All specimens from the patients were fixed in 10% neutral buffered formalin and embedded in paraffin. The mutational status of IDH1/2 and the TERT promoter was determined using polymerase chain reaction-based direct sequencing. The assay for the 1p and 19q co-deletion was conducted using fluorescence in situ hybridization. Overall- and progression-free survival was calculated using the Kaplan–Meier method and the log-rank test. The study was approved by the Ethics Committee of Xuanwu Hospital, Capital Medical University, China (approval No. [2019]004) on May 22, 2019. Results: We found that tumors characterized by multiple lesions were predominantly free of IDH mutations (P < 0.001). Gliomas with IDH mutations arose more often in the frontal and insular lobes than in the other lobes (P < 0.001). Rates of IDH mutations were higher in patients who had seizures or were without discomfort than in those who had other clinical symptoms (P = 0.0003). Of 119 patients with complete molecular information according to the 2016 World Health Organization classification of central nervous system tumors, 5 had oligoastrocytomas that had multiple genotypes – IDH1 mutation, loss of ATRX expression, and 1p/19q co-deletion – but lacked TERT promoter mutations. Patients with seizures or without discomfort who had IDH mutations had better outcomes than did other patients (P < 0.001). Patients whose tumors had IDH and TERT promoter mutations had a better prognosis than did other patients (P < 0.001). Among patients whose tumors had wild-type IDH, those with loss of ATRX survived longer than did others (P = 0.005). Conclusions: The status of both ATRX and the TERT promoter can indicate the prognosis in patients with IDH wild-type gliomas. The diagnosis that is based on clinical symptoms, histologic findings, and molecular analysis should be implemented as the diagnostic standard for patients with oligoastrocytomas.
背景与目的:异柠檬酸脱氢酶(IDH)的突变、1p和19q的共缺失、转录调节因子ATRX的缺失或表达以及端粒酶逆转录酶(TERT)基因启动子的突变与弥漫性胶质瘤密切相关。我们进一步探讨了关键分子在成年弥漫性胶质瘤中的作用及其预后。材料与方法:本观察性研究纳入2009年至2015年在中国北京宣武医院接受初次手术的413例患者。所有患者标本均用10%中性缓冲福尔马林固定,石蜡包埋。采用基于聚合酶链反应的直接测序方法确定IDH1/2和TERT启动子的突变状态。采用荧光原位杂交法检测1p和19q共缺失。总生存期和无进展生存期采用Kaplan-Meier法和log-rank检验计算。本研究经中国首都医科大学宣武医院伦理委员会批准(批准号:[2019]004)于2019年5月22日发布。结果:我们发现以多发病变为特征的肿瘤主要不存在IDH突变(P < 0.001)。IDH突变的胶质瘤在额叶和岛叶的发生率高于其他脑叶(P < 0.001)。癫痫发作或无不适的患者的IDH突变率高于有其他临床症状的患者(P = 0.0003)。根据2016年世界卫生组织中枢神经系统肿瘤分类,在119例具有完整分子信息的患者中,有5例具有多种基因型(IDH1突变、ATRX表达缺失和1p/19q共缺失)的少星形细胞瘤,但缺乏TERT启动子突变。有癫痫发作或无不适的IDH突变患者的预后优于其他患者(P < 0.001)。肿瘤发生IDH和TERT启动子突变的患者预后优于其他患者(P < 0.001)。在肿瘤为野生型IDH的患者中,ATRX缺失的患者比其他患者存活时间更长(P = 0.005)。结论:ATRX和TERT启动子的状态可以指示IDH野生型胶质瘤患者的预后。基于临床症状、组织学表现和分子分析的诊断应作为寡星形细胞瘤患者的诊断标准。
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引用次数: 0
Mechanisms of cell competition in glioblastoma: A narrative review 胶质母细胞瘤细胞竞争机制的叙述性综述
Pub Date : 2020-10-01 DOI: 10.4103/glioma.glioma_29_20
Paramita Kundu, V. Santosh, P. Kondaiah
Cell competition among neighboring cells in a tissue gauges relative fitness in terms of growth and proliferation, which results in the death of cells with suboptimal fitness and the dominance of optimally or supraoptimally fit cells. It is conserved across multiple taxa and has indispensable functions in development, homeostasis, aging, and prevention of neoplastic growth, both in Drosophila and mammals. However, similar to how several key developmental pathways are subverted in cancer, cell competition mechanisms are often co-opted in the oncogenic transformation of cells in homeostatically stable tissues, and the role of this phenomenon in human cancer is attracting increasing interest. Grade IV glioblastomas (GBMs) are the most aggressive brain tumors that occur in adults. GBMs arise from glial cells and invariably result in tumor recurrence and death. Treatment of GBMs is complicated by the unique features of the anatomical context, including the dura, blood–brain barrier, glioma stem cells, necrosis, and extensive genetic and epigenetic heterogeneity. In this review, we discuss the evidence for cell competition elicited by genomic alterations in several key genes involved in early or late gliomagenesis, as well as activation of specific signaling pathways that aid competitive interactions with nonglial cell types like neurons to gain leverage in the colonization of brain niches. The role of intratumoral heterogeneity in conferring clonal dominance or cooperation resulting in therapeutic resistance in GBMs is also discussed.
组织中相邻细胞之间的细胞竞争衡量生长和增殖方面的相对适应度,这导致适应度次优的细胞死亡,以及最佳或超最佳适应度细胞的优势。它在多个分类群中是保守的,在果蝇和哺乳动物的发育、体内平衡、衰老和预防肿瘤生长方面具有不可或缺的功能。然而,与癌症中几种关键发育途径被破坏的情况类似,细胞竞争机制通常在稳态稳定组织中的细胞的致癌转化中同时存在,这种现象在人类癌症中的作用越来越引起人们的兴趣。IV级胶质母细胞瘤(GBMs)是发生在成人中最具侵袭性的脑肿瘤。GBMs来源于神经胶质细胞,总是导致肿瘤复发和死亡。GBMs的治疗因解剖环境的独特特征而变得复杂,包括硬脑膜、血脑屏障、神经胶质瘤干细胞、坏死以及广泛的遗传和表观遗传学异质性。在这篇综述中,我们讨论了参与早期或晚期胶质瘤的几个关键基因的基因组改变引发的细胞竞争的证据,以及特定信号通路的激活,这些通路有助于与神经元等非胶质细胞类型的竞争性相互作用,以在脑小生境的定殖中获得优势。还讨论了肿瘤内异质性在赋予GBMs克隆优势或合作导致治疗耐药性中的作用。
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引用次数: 1
Particle radiation therapy in the management of adult high-grade glioma: A narrative review 粒子放射治疗在成人高级别胶质瘤中的应用:综述
Pub Date : 2020-10-01 DOI: 10.4103/glioma.glioma_30_20
L. Kong, Jiade J. Lu
This narrative review summarizes the current status of the use of particle radiation therapy on the treatment of adult malignant gliomas. Due to the unique physical property, particle (e.g., proton or carbon-ion) beam radiation therapy can improve radiation dose distribution, thereby therapeutic radio for patients with brain malignancy. Therefore, particle beam radiation therapy is associated with low adverse events which have implications for improving quality of life for long-term survivors. In addition, there is a potential for safe dose escalation in selected patients. Malignant glioma is considered radioresistant; thus, particle beams of higher relative biological effectiveness, carbon-ion beam, for example, may further improve disease control in theory. Data on carbon-ion beam RT alone for the management of brain tumor are scarce. Most literature described proton beam alone or the use of combined proton/photon and carbon-ion beam boost for the treatment of glioma. Existing clinical evidence describes virtually no acute high-grade toxicities and limited late effects. Prospective clinical trials are needed to confirm the improved efficacy and favorable toxicity profile of particle beam radiation therapy on adult malignant glioma described in retrospective studies. Currently, multiple prospective trials are ongoing to answer such questions.
本文综述了粒子放射治疗成人恶性胶质瘤的应用现状。由于其独特的物理性质,粒子(如质子或碳离子)束放射治疗可以改善辐射剂量分布,从而为脑恶性肿瘤患者提供治疗性放疗。因此,粒子束放射治疗与低不良事件相关,这对提高长期幸存者的生活质量具有意义。此外,在选定的患者中存在安全剂量增加的可能性。恶性胶质瘤被认为具有抗辐射性;因此,相对生物有效性较高的粒子束,例如碳离子束,在理论上可以进一步改善疾病控制。关于碳离子束RT单独用于脑肿瘤治疗的数据很少。大多数文献描述了单独使用质子束或结合使用质子/光子和碳离子束增强治疗神经胶质瘤。现有的临床证据表明,几乎没有急性高级别毒性,后期效果有限。需要进行前瞻性临床试验来证实回顾性研究中描述的粒子束放射治疗成人恶性胶质瘤的疗效和良好的毒性。目前,正在进行多项前瞻性试验来回答这些问题。
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引用次数: 0
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Glioma
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