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Malignant pineal germ-cell tumors: An analysis of cases from three tumor registries

机译:恶性松果体生殖细胞肿瘤:来自三个肿瘤登记处的病例分析

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The exact incidence of pineal germ-cell tumors is largely unknown. The tumors are rare, and the number of patients with these tumors, as reported in clinical series, has been limited. The goal of this study was to describe pineal germ-cell tumors in a large number of patients, using data from available brain tumor databases. Three different databases were used: Surveillance, Epidemiology, and End Results (SEER) database (1973-2001); Central Brain Tumor Registry of the United States (CBTRUS; 1997-2001); and National Cancer Data Base (NCDB; 1985-2003). Tumors were identified using the International Classification of Diseases for Oncology, third edition (ICD-O-3), site code C75.3, and categorized according to histology codes 9060-9085. Data were analyzed using SAS/STAT release 8.2, SEER~*Stat version 5.2, and SPSS version 13.0 software. A total of 1,467 cases of malignant pineal germ-cell tumors were identified: 1,159 from NCDB, 196 from SEER, and 112 from CBTRUS. All three databases showed a male predominance for pineal germ-cell tumors ( > 90%), and >72% of patients were Caucasian. The peak number of cases occurred in the 10- to 14-year age group in the CBTRUS data and in the 15- to 19-year age group in the SEER and NCDB data, and declined significantly thereafter. The majority of tumors (73%-86%) were germinomas, and patients with germinomas had the highest survival rate ( > 79% at 5 years). Most patients were treated with surgical resection and radiation therapy or with radiation therapy alone. The number of patients included in this study exceeds that of any study published to date. The proportions of malignant pineal germ-cell tumors and intracranial germ-cell tumors are in range with previous studies. Survival rates for malignant pineal germ-cell tumors are lower than results from recent treatment trials for intracranial germ-cell tumors, and patients that received radiation therapy in the treatment plan either with surgery or alone survived the longest.
机译:松果生殖细胞肿瘤的确切发病率在很大程度上尚不清楚。肿瘤是罕见的,并且如临床系列中所报道的,患有这些肿瘤的患者数量受到限制。这项研究的目的是使用来自可用脑肿瘤数据库的数据来描述大量患者的松果生殖细胞肿瘤。使用了三个不同的数据库:监测,流行病学和最终结果(SEER)数据库(1973-2001);美国中央脑肿瘤登记处(CBTRUS; 1997-2001);美国国家癌症数据库(NCDB; 1985-2003年)。使用《国际肿瘤分类学》(ICD-O-3)第三版(CD5.3)识别肿瘤,并根据组织学代码9060-9085进行分类。使用SAS / STAT版本8.2,SEER〜* Stat版本5.2和SPSS版本13.0软件分析数据。总共鉴定出1,467例恶性松果生殖细胞肿瘤:NCDB 1,159例,SEER 196例,CBTRUS 112例。这三个数据库均显示男性占松果生殖细胞肿瘤的主导地位(> 90%),并且> 72%的患者为白种人。 CBTRUS数据中10至14岁年龄段的病例最多,SEER和NCDB数据中15至19岁年龄段的病例最多,此后显着下降。大多数肿瘤(73%-86%)是生殖器瘤,生殖器瘤患者的生存率最高(5年时> 79%)。大多数患者接受手术切除和放射治疗或仅接受放射治疗。这项研究中包括的患者人数超过了迄今为止发表的任何研究的人数。恶性松果体生殖细胞肿瘤和颅内生殖细胞肿瘤的比例在以前的研究范围内。恶性松果体生殖细胞肿瘤的存活率低于最近颅内生殖细胞肿瘤的治疗试验的结果,并且在接受了放射疗法治疗的患者中,无论是手术治疗还是单独接受手术治疗的患者,存活时间最长。

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