法图玛-布尔吉巴大学莫纳斯提尔医院肿瘤内科治疗恶性胶质瘤20例

Hiba Sboui, A. Daldoul, Nader Slema, Amal Chamsi, S. Zaied
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引用次数: 0

摘要

简介:恶性胶质瘤是指根据世界卫生组织(世界卫生组织)分类定义的III级或IV级脑肿瘤。它们是一组异质性的病理,从其频率、严重程度和治疗困难来看,是一个严重的健康问题。尽管医学取得了很大进展,恶性胶质瘤的预后仍然很差。材料和方法:这是一项回顾性研究,根据STUPP方案,纳入了2012年至2016年间在莫纳斯提尔Fattouma Bourguiba医院肿瘤内科治疗的20例恶性胶质瘤。结果:12名男性和8名女性,中位年龄为43岁。临床症状不是很具体,主要是颅内高压和缺损症状。影像学指的是对恶性胶质瘤的诊断。手术包括(15%)例的宏观完全用力,(50%)例的部分用力,其余患者进行立体定向活检。组织学发现16例(80%)、2例III级间变性星形细胞瘤(10%)、1例间变性少突胶质瘤(5%)和1例III级间变性eppendymoma(5%)存在GBM。我们的大多数患者同时接受了放射化疗,15名患者接受了TMZ辅助化疗,其中7人接受了全部6次预定治疗。在12名复发患者中,只有一名患者决定接受复发治疗。6名患者仍然活着。中位生存期为11.27个月。在我们的系列中,总生存率与组织学类型(p=0.006)和RT-CT结束时评估的神经状态(p=0.001)有关。尽管生存率与评估的标准一致,但年龄、一般情况评分、手术类型和治疗后发展没有显示出统计学上的显著关系。结论:恶性胶质瘤是一种罕见的肿瘤,预后不良,在突尼斯因诊断延误而加重。建立一个多学科的神经肿瘤学小组可以帮助改善管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of Malignants Gliomas: About 20 Cases Treated in the Medical Oncology Department of Fattouma Bourguiba University Hospital-Monastir
Introduction: Malignant gliomas refer to grade III or IV brain tumors defined according to the World Health Organization (WHO) classification. They are a heterogeneous group of pathologies and represent a serious health problem by their frequency, severity and treatment difficulties. The prognosis of malignant gliomas remains poor despite all the medical advances. Materials and Methods: It is a retrospective study included 20 cases of malignant glial tumors treated at the medical oncology department, Fattouma Bourguiba hospital in Monastir between 2012 and 2016, according to the STUPP protocol. Results: These were 12 men and 8 women with a median age of 43. Clinical signs were not very specific, dominated by intracranial hypertension and deficit signs. Imagery referred to the diagnosis of malignant gliomas in 1st intention. Surgery consisted of a macroscopically complete exeresis in (15%) cases, a partial exeresis in (50%), the rest of the patients had a stereotactic biopsy. Histology found GBM in 16 patients (80%), 2 cases of Grade III anaplastic astrocytoma (10%), 1 case of anaplastic oligodendroglioma (5%), and 1 case of Grade III anaplastic eppendymoma (5%). Most of our patients received concurrent radio-chemotherapy and adjuvant TMZ chemotherapy was administered in 15 patients, 7 of whom received the full 6 scheduled cures. A relapse treatment was decided in only one of the 12 patients who relapsed. 6 patients are still alive. The median survival is 11.27 months. In our series, overall survival was related to histological type (p = 0.006) and neurological status assessed at the end of RT-CT (p = 0.001). While age, general condition score, type of surgery, and post-therapeutic development did not show a statistically significant relationship, although survival rates were consistent with the criteria assessed. Conclusion: Malignant gliomas are rare tumors, bad prognosis, aggravated in Tunisia by a diagnostic delay. The creation of a multidisciplinary neuro-oncology group can help to improve management.
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