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丹麦神经肿瘤注册研究 2009-2014 年:胶质母细胞瘤患者的治疗和生存情况。

Treatment and survival of glioblastoma patients in Denmark: The Danish Neuro-Oncology Registry 2009-2014.

机构信息

Department of Oncology, Odense University Hospital, Odense, Denmark.

Institute of Clinical Research, University of Southern Denmark, Odense, Denmark.

出版信息

J Neurooncol. 2018 Sep;139(2):479-489. doi: 10.1007/s11060-018-2892-7. Epub 2018 May 12.

Abstract

BACKGROUND

As many glioblastoma patients are in a poor condition they are unable to undergo the full treatment documented in clinical trials. We aimed to examine the survival and its relationship to clinical characteristics and treatment in a nationwide population of glioblastoma patients in Denmark.

METHODS

We included prospectively recorded clinical data from 1364 adult patients with histologically verified glioblastoma from the Danish Neuro-Oncology Registry, 2009-2014.

RESULTS

The age standardized incidence rate was 6.3/100,000 person-years for males and 3.9 for females and the median age was 66 years. The median overall survival was 11.2 months. There was an independently significant prognostic effect of age, performance status, cognitive symptoms, tumor diameter, multifocality, crossing midline, and contrast enhancement. For partial and total resection compared to biopsy only, the adjusted risk of dying was reduced by 43% (HR [CI] 0.57 [0.48-0.68]) and 51% (0.49 [0.40-0.60]), respectively. For patients receiving a partial and full radiochemotherapy regimen compared to no postsurgical treatment, the risk reduction was 56% (HR [CI] 0.44 [0.37-0.53]) and 70% (0.30 [0.25-0.35]), respectively. The full radiochemotherapy regimen was only allocated to 50% of the patients, 29% among the oldest (70+ years) and 60% among the younger (18-69 years).

CONCLUSIONS

Glioblastoma patients had a poor overall survival but with several specific independent prognostic factors. Extensive cancer treatment was associated with an increasing survival in all age groups, but only half of the patients were sufficiently fit for a full regimen of postoperative combined radiochemotherapy.

摘要

背景

由于许多胶质母细胞瘤患者身体状况不佳,无法接受临床试验中记录的完整治疗。我们旨在检查丹麦全国范围内胶质母细胞瘤患者的生存情况及其与临床特征和治疗的关系。

方法

我们纳入了 2009 年至 2014 年期间来自丹麦神经肿瘤登记处的 1364 名经组织学证实的成人胶质母细胞瘤患者的前瞻性记录的临床数据。

结果

男性的年龄标准化发病率为 6.3/100,000 人年,女性为 3.9/100,000 人年,中位年龄为 66 岁。中位总生存期为 11.2 个月。年龄、表现状态、认知症状、肿瘤直径、多灶性、中线穿越和对比增强均具有独立的预后意义。与单纯活检相比,部分切除和全切除的死亡风险分别降低了 43%(HR[CI]0.57[0.48-0.68])和 51%(0.49[0.40-0.60])。与未接受术后治疗的患者相比,接受部分和全放化疗方案的患者死亡风险分别降低了 56%(HR[CI]0.44[0.37-0.53])和 70%(0.30[0.25-0.35])。全放化疗方案仅分配给 50%的患者,其中年龄最大的(70+岁)患者占 29%,年龄最小的(18-69 岁)患者占 60%。

结论

胶质母细胞瘤患者的总体生存情况较差,但具有几个特定的独立预后因素。广泛的癌症治疗与所有年龄段的生存增加相关,但只有一半的患者适合接受术后联合放化疗的全疗程。

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