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原发性中枢神经系统淋巴瘤与多形性胶质母细胞瘤的诊断延迟及预后比较。

Diagnostic delay and prognosis in primary central nervous system lymphoma compared with glioblastoma multiforme.

作者信息

Cerqua R, Balestrini S, Perozzi C, Cameriere V, Renzi S, Lagalla G, Mancini G, Montanari M, Leoni P, Scerrati M, Iacoangeli M, Silvestrini M, Luzzi S, Provinciali L

机构信息

Department of Experimental and Clinical Medicine, Neurological Clinic, Marche Polytechnic University, via Conca 71, 60020, Ancona, Italy.

Hematology Department, Marche Polytechnic University, Ancona, Italy.

出版信息

Neurol Sci. 2016 Jan;37(1):23-29. doi: 10.1007/s10072-015-2353-4. Epub 2015 Aug 2.

DOI:10.1007/s10072-015-2353-4
PMID:26233232
Abstract

Glioblastoma multiforme (GBM) and primary central nervous system lymphoma (PCNSL) are malignant cerebral neoplasms associated with poor prognosis. Early diagnosis and subsequent planning of adequate treatment strategy are relevant to improve survival and reduce neurological deficit. Two groups of patients affected by GBM and PCNSL were compared to identify: (1) factors influencing the time necessary to obtain a correct diagnosis; (2) the influence of the interval time from clinical onset to diagnosis on the prognosis. Fifty-six patients (28 PCNSL and 28 GBM, 23 females and 33 males) referred to the same hospital setting were retrospectively evaluated. The mean age at diagnosis was 61 years. The two groups were comparable in terms of age, sex, clinical symptoms at onset and performance status. There was no relevant difference in time span from clinical onset to first neuroimaging examination, while time span from first neuroimaging to final morphological diagnosis was much longer in PCNSL patients (p = 0.008). Multivariate Cox regression analysis, including both PCNSL and GBM cases, showed a significant association of the overall survival with: time to diagnosis (HR 0.06), age at onset (HR 1.04). Our results show a significant diagnostic delay in PCNSL cases. Age at onset of disease and time to diagnosis emerge as clinical factors affecting overall survival in both groups. Stereotactic-guided biopsy should be chosen as routine method to early diagnose PCNSL. The clinical relevance of early diagnosis in GBM and PCNSL needs to be emphasized to maximize the overall survival in both neoplasms.

摘要

多形性胶质母细胞瘤(GBM)和原发性中枢神经系统淋巴瘤(PCNSL)是预后较差的恶性脑肿瘤。早期诊断及随后制定适当的治疗策略对于提高生存率和减少神经功能缺损至关重要。对两组分别患有GBM和PCNSL的患者进行比较,以确定:(1)影响获得正确诊断所需时间的因素;(2)从临床发病到诊断的间隔时间对预后的影响。对转诊至同一医院的56例患者(28例PCNSL和28例GBM,23例女性和33例男性)进行了回顾性评估。诊断时的平均年龄为61岁。两组在年龄、性别、发病时的临床症状及体能状态方面具有可比性。从临床发病到首次神经影像学检查的时间跨度无显著差异,而PCNSL患者从首次神经影像学检查到最终形态学诊断的时间跨度要长得多(p = 0.008)。包括PCNSL和GBM病例的多变量Cox回归分析显示,总生存期与以下因素显著相关:诊断时间(HR 0.06)、发病年龄(HR 1.04)。我们的结果显示PCNSL病例存在显著的诊断延迟。发病年龄和诊断时间是影响两组总生存期的临床因素。应选择立体定向引导活检作为早期诊断PCNSL的常规方法。需要强调GBM和PCNSL早期诊断的临床相关性,以最大限度提高这两种肿瘤的总生存期。

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