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幕上低级别胶质瘤成年患者的长期生存进展:一项基于人群的研究,研究对象为993例于1970年至1993年间被诊断出患有肿瘤的患者。

Progress in long-term survival in adult patients with supratentorial low-grade gliomas: a population-based study of 993 patients in whom tumors were diagnosed between 1970 and 1993.

作者信息

Johannesen Tom B, Langmark Frøydis, Lote Knut

机构信息

Norwegian Cancer Registry, Institute of Population-Based Cancer Research, Oslo, Norway.

出版信息

J Neurosurg. 2003 Nov;99(5):854-62. doi: 10.3171/jns.2003.99.5.0854.

Abstract

OBJECT

The goal of this study was to document and compare long-term survival during the periods 1970 through 1981 and 1982 through 1993 in all adult patients in Norway with histologically verified supratentorial low-grade gliomas (LGGs).

METHODS

Nine hundred ninety-three patients 15 to 69 years of age were found to have a primary supratentorial diffuse astrocytoma, oligodendroglioma, oligoastrocytoma, or pilocytic astrocytoma. Survival time was analyzed in all patients and, in a subset of 451 patients, the influence of new imaging methods on the time from symptom onset to imaging diagnosis was estimated. Overall median survival was 6.4 years (95% confidence interval [CI] 5.7-7.1 years). Survival times for patients in whom a diagnosis was made between 1970 and 1981 (397 patients) and between 1982 and 1993 (596 patients) were 4.1 years (95% CI 3.3-4.9 years) and 9.2 years (95% CI 7.9-10.6 years), respectively (p < 0.0001). Survival also improved in the later period within each histological subgroup. In patients in whom a biopsy was performed the median length of survival was 6.4 years (95% CI 3.1-9.7 years); in patients treated with subtotal tumor resection it was 6.8 years (95% CI 5.8-7.7 years); and in those treated with gross-total tumor resection it was 7.6 years (95% CI 5.5-9.7 years), a nonsignificant difference (p = 0.59). A considerable age-dependent variation in overall survival was demonstrated. The availability of computerized tomography (CT) scanning and/or magnetic resonance (MR) imaging as a diagnostic tool reduced the median period of symptoms prior to diagnosis by 6 months.

CONCLUSIONS

Long-term overall survival significantly improved, but age-related differences in prognosis persisted. The increased sensitivity of the diagnostic method due to the availability of CT scanning and/or MR imaging may partly, but not entirely, account for the observed magnitude of improvement in overall survival. Thus local tumor treatment improved during the study period.

摘要

目的

本研究的目的是记录并比较1970年至1981年以及1982年至1993年期间挪威所有经组织学证实的幕上低级别胶质瘤(LGG)成年患者的长期生存率。

方法

发现993例年龄在15至69岁之间的患者患有原发性幕上弥漫性星形细胞瘤、少突胶质细胞瘤、少突星形细胞瘤或毛细胞型星形细胞瘤。对所有患者的生存时间进行了分析,并在451例患者的子集中,估计了新成像方法对从症状出现到成像诊断时间的影响。总体中位生存期为6.4年(95%置信区间[CI]5.7 - 7.1年)。1970年至1981年期间确诊的患者(397例)和1982年至1993年期间确诊的患者(596例)的生存时间分别为4.1年(95%CI 3.3 - 4.9年)和9.2年(95%CI 7.9 - 10.6年)(p < 0.0001)。在每个组织学亚组中,后期的生存率也有所提高。接受活检的患者中位生存时长为6.4年(95%CI 3.1 - 9.7年);接受肿瘤次全切除的患者为6.8年(95%CI 5.8 - 7.7年);接受肿瘤全切除的患者为7.6年(95%CI 5.5 - 9.7年),差异无统计学意义(p = 0.59)。总体生存显示出明显的年龄依赖性差异。计算机断层扫描(CT)和/或磁共振成像(MR)作为诊断工具的应用使诊断前症状的中位时长缩短了6个月。

结论

长期总体生存率显著提高,但预后的年龄相关差异仍然存在。由于CT扫描和/或MR成像的应用导致诊断方法敏感性增加,这可能部分但并非完全解释了观察到的总体生存率提高的幅度。因此,在研究期间局部肿瘤治疗有所改善。

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