Villano J Lee, Propp Jennifer M, Porter Kimberly R, Stewart Andrew K, Valyi-Nagy Tibor, Li Xinyu, Engelhard Herbert H, McCarthy Bridget J
Department of Epidemiology/Biostatistics, School of Public Health, University of Illinois at Chicago, 1603 W. Taylor Street, Chicago, IL 60612, USA.
Neuro Oncol. 2008 Apr;10(2):121-30. doi: 10.1215/15228517-2007-054. Epub 2008 Feb 20.
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.
松果体生殖细胞肿瘤的确切发病率很大程度上尚不清楚。这些肿瘤很罕见,临床系列报道的此类肿瘤患者数量有限。本研究的目的是利用现有脑肿瘤数据库的数据,描述大量患者的松果体生殖细胞肿瘤情况。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年);美国中央脑肿瘤登记处(CBTRUS;1997 - 2001年);以及国家癌症数据库(NCDB;1985 - 2003年)。使用国际肿瘤疾病分类第三版(ICD - O - 3)部位编码C75.3识别肿瘤,并根据组织学编码9060 - 9085进行分类。使用SAS/STAT 8.2版、SEER*Stat 5.2版和SPSS 13.0版软件进行数据分析。共识别出1467例恶性松果体生殖细胞肿瘤病例:1159例来自NCDB,196例来自SEER,112例来自CBTRUS。所有三个数据库均显示松果体生殖细胞肿瘤以男性为主(>90%),且>72%的患者为白种人。CBTRUS数据中病例数峰值出现在10至14岁年龄组,SEER和NCDB数据中则出现在15至19岁年龄组,此后显著下降。大多数肿瘤(73% - 86%)为生殖细胞瘤,生殖细胞瘤患者的生存率最高(5年时>79%)。大多数患者接受了手术切除加放射治疗或仅接受放射治疗。本研究纳入的患者数量超过了迄今发表的任何研究。恶性松果体生殖细胞肿瘤和颅内生殖细胞肿瘤的比例与先前研究一致。恶性松果体生殖细胞肿瘤的生存率低于近期颅内生殖细胞肿瘤治疗试验的结果,在治疗方案中接受放射治疗(无论是否联合手术)的患者存活时间最长。