Goodwin Tress L, Sainani Kristin, Fisher Paul Graham
Stanford University School of Medicine Department of Health Research and Policy, Stanford University School of Medicine, Stanford, CA 94305-5826, USA.
J Pediatr Hematol Oncol. 2009 Aug;31(8):541-4. doi: 10.1097/MPH.0b013e3181983af5.
Incidence patterns of central nervous system (CNS) germ cell tumors (GCTs) have been reported, but the influence of underlying host risk factors has not been rigorously explored. We aimed to determine in a large, population-based cancer registry how age, sex, and race, influence the occurrence of CNS GCTs in the pediatric population.
Using the Surveillance, Epidemiology, and End Results registry, we identified cases of histologically confirmed GCTs in children, adolescents, and young adults (age 0 to 29 y), diagnosed between 1973 and 2004. The cases were limited to only those with the International Classification of Childhood Cancer Xa: intracranial and intraspinal germ-cell tumors. Incidence rates (per 10,000) for each sex and race were plotted for single-age groups, and then stratified by tumor location and pathology subtype.
The sample included a total of 638 cases (490 males). Males had significantly higher rates of CNS GCTs than females. Male and female rates diverged significantly starting at the age of 11 years and remained widely discrepant until the age of 30 years. There were more germinomas than nongerminomas in both sexes. Germinomas peaked in incidence during adolescence, whereas nongerminoma incidence remained relatively constant in children and young adults. Tumor location differed strikingly by sex (P<0.0001) with pineal location more common in males (61.0% vs. 15.5%). Asian race was associated with a higher rate of CNS GCTs than other races.
Males have higher incidence of CNS GCTs, primarily germinomas, than females, starting in the second decade. Pineal location is strongly associated with male sex, with pineal germinomas representing over half of all CNS GCTs in males. Asian-Americans have higher rates than other races. These findings suggest a robust but poorly understood influence of sex, either genetic or hormonal, and race on the occurrence of CNS GCTs.
中枢神经系统(CNS)生殖细胞肿瘤(GCTs)的发病率模式已有报道,但潜在宿主风险因素的影响尚未得到严格探究。我们旨在通过一个大型的基于人群的癌症登记处,确定年龄、性别和种族如何影响儿科人群中CNS GCTs的发生。
利用监测、流行病学和最终结果登记处的数据,我们确定了1973年至2004年间诊断的儿童、青少年和年轻成人(0至29岁)中组织学确诊的GCTs病例。这些病例仅限于国际儿童癌症分类Xa:颅内和脊髓生殖细胞肿瘤。绘制了每个性别和种族单一年龄组的发病率(每10000人),然后按肿瘤位置和病理亚型进行分层。
样本共包括638例病例(490例男性)。男性CNS GCTs的发病率显著高于女性。男性和女性的发病率在11岁时开始出现显著差异,并在30岁之前一直存在很大差异。两性中生殖细胞瘤均多于非生殖细胞瘤。生殖细胞瘤的发病率在青春期达到峰值,而非生殖细胞瘤在儿童和年轻成人中的发病率相对保持稳定。肿瘤位置在性别上有显著差异(P<0.0001),松果体部位在男性中更常见(61.0%对15.5%)。亚洲种族CNS GCTs的发病率高于其他种族。
从第二个十年开始,男性CNS GCTs的发病率高于女性,主要是生殖细胞瘤。松果体部位与男性密切相关,松果体生殖细胞瘤占男性所有CNS GCTs的一半以上。亚裔美国人的发病率高于其他种族。这些发现表明性别(无论是遗传还是激素方面)和种族对CNS GCTs的发生有强大但尚未完全理解的影响。