中国单个机构新诊断的胶质瘤患者的真实世界管理和生存结果:一项回顾性队列研究

Glioma Pub Date : 2019-03-01 DOI:10.4103/glioma.glioma_14_19
Depei Li, Yinsheng Chen, Chengcheng Guo, Xiangheng Zhang, K. Sai, Chao Ke, Ji Zhang, Xiaobing Jiang, Zheng-he Chen, Fu-Hua Lin, Qunying Yang, Jian Wang, Yong-gao Mu, Zhongping Chen
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引用次数: 2

摘要

背景和目的:指南建议对进展风险高的高级别胶质瘤和低级别胶质瘤患者进行辅助治疗。然而,在临床实践中,治疗可能不符合这些建议的指南。在这项研究中,我们回顾了中国中山大学癌症中心(SYSUCC)胶质瘤患者的治疗和结果。材料与方法:回顾性分析2000年至2017年在该中心接受手术的1215例神经胶质瘤患者的病历和放射学图像,并分析其临床病理特征、治疗方法和总生存率。该研究于2019年2月20日获得了SYSUCC伦理委员会的批准(批准号:GZR2019-219)。结果:共有1001名被诊断为神经胶质瘤的患者(最初为世界卫生组织2007年标准,然后为2016年标准)入选,其中90名患者为一级,307名为二级,239名为三级,365名为四级。604例高级胶质瘤患者中有331例(54.8%)和397例低级胶质瘤患者(40.1%)接受了术后放疗,285例高级肿瘤患者(47.1%)和80例低级肿瘤患者(20.2%)接受了辅助化疗。IV级胶质瘤的中位OS为17.5个月,III级胶质瘤为43.1个月。未达到低度胶质瘤患者的中位OS。I、II、III和IV级胶质瘤患者的5年生存率分别为94.7%、73.7%、45.7%和18.6%。多因素分析确定,发病年龄、术前癫痫发作、肿瘤位置、病理亚型、切除范围和术后治疗是高级别胶质瘤患者OS的独立预测因素。接受术后治疗的高级别胶质瘤患者的生存率高于未接受辅助治疗的患者(III级:52.6 vs.20.3个月,P=0.012;IV级:22.6 vs.12.1个月,P<0.001)。在弥漫性低级别胶质瘤的患者中,年龄、表现状态、术前癫痫发作、Ki-67指数、肿瘤亚型和切除程度与临床结果相关。结论:胶质瘤患者并非总是按照指导方针进行治疗。尽管标准护理可能会带来良好的预后,但个体化治疗可能更容易接受,并产生更好的结果,因此应在常规临床实践中予以考虑。
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Real-world management and survival outcomes of patients with newly diagnosed gliomas from a single institution in China: A retrospective cohort study
Background and Aim: Guidelines recommend adjuvant treatment for patients with high-grade gliomas and low-grade gliomas with high risk of progression. In clinical practice, however, treatments may not conform to these suggested guidelines. In this study, we reviewed the treatments and outcomes in patients with gliomas at Sun Yat-Sen University Cancer Center (SYSUCC), China. Materials and Methods: Medical records and radiologic images of 1215 glioma patients who underwent surgery at the center from 2000 to 2017 were retrospectively reviewed, and their clinicopathological characteristics, treatment method, and overall survival (OS) were analyzed. The study was approved by the Ethics Committee of SYSUCC on February 20, 2019 (approval No. GZR2019-219). Results: A total of 1001 patients diagnosed with glioma (initially World Health Organization 2007 criteria, then 2016 criteria) were enrolled, including 90 patients with Grade I, 307 Grade II, 239 Grade III, and 365 Grade IV gliomas. A total of 331 of 604 patients with high-grade glioma (54.8%) and 159 of 397 with low-grade glioma (40.1%) received postsurgical radiotherapy, and 285 patients with high-grade tumors (47.1%) and 80 with low-grade tumors (20.2%) received adjuvant chemotherapy. The median OS was 17.5 months for Grade IV and 43.1 months for Grade III gliomas. The median OS of patients with low-grade glioma was not reached. The 5-year survival rates of patients with Grades I, II, III, and IV gliomas were 94.7%, 73.7%, 45.7%, and 18.6%, respectively. Multivariate analysis identified onset age, preoperative seizure, tumor location, pathological subtype, resection extent, and postsurgical treatment as independent predictors of OS in patients with high-grade gliomas. Patients with high-grade glioma who received postsurgical treatment had better survival than those without adjuvant therapy (Grade III: 52.6 vs. 20.3 months, P = 0.012; Grade IV: 22.6 vs. 12.1 months, P < 0.001). Among patients with diffuse low-grade gliomas, age, performance status, preoperative seizure, Ki-67 index, tumor subtype, and resection extent were associated with clinical outcomes. Conclusion: Glioma patients are not always treated according to guidelines. Although standard care may lead to favorable prognoses, individualized treatments may be more acceptable and result in better outcomes and should thus be considered in routine clinical practice.
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