Schraw Jeremy M, Desrosiers Tania A, Nembhard Wendy N, Langlois Peter H, Meyer Robert E, Canfield Mark A, Rasmussen Sonja A, Chambers Tiffany M, Spector Logan G, Plon Sharon E, Lupo Philip J
Department of Medicine, Baylor College of Medicine, Houston, Texas.
Center for Epidemiology and Population Health, Baylor College of Medicine, Houston, Texas.
Cancer. 2020 Aug 1;126(15):3483-3492. doi: 10.1002/cncr.32982. Epub 2020 May 29.
Birth defects are established risk factors for childhood cancer. Nonetheless, cancer epidemiology in children with birth defects is not well characterized.
Using data from population-based registries in 4 US states, this study compared children with cancer but no birth defects (n = 13,111) with children with cancer and 1 or more nonsyndromic birth defects (n = 1616). The objective was to evaluate cancer diagnostic characteristics, including tumor type, age at diagnosis, and stage at diagnosis.
Compared with the general population of children with cancer, children with birth defects were diagnosed with more embryonal tumors (26.6% vs 18.7%; q < 0.001), including neuroblastoma (12.5% vs 8.2%; q < 0.001) and hepatoblastoma (5.0% vs 1.3%; q < 0.001), but fewer hematologic malignancies, including acute lymphoblastic leukemia (12.4% vs 24.4%; q < 0.001). In age-stratified analyses, differences in tumor type were evident among children younger than 1 year and children 1 to 4 years old, but they were attenuated among children 5 years of age or older. The age at diagnosis was younger in children with birth defects for most cancers, including leukemia, lymphoma, astrocytoma, medulloblastoma, ependymoma, embryonal tumors, and germ cell tumors (all q < 0.05).
The results indicate possible etiologic heterogeneity in children with birth defects, have implications for future surveillance efforts, and raise the possibility of differential cancer ascertainment in children with birth defects.
Scientific studies suggest that children with birth defects are at increased risk for cancer. However, these studies have not been able to determine whether important tumor characteristics, such as the type of tumor diagnosed, the age at which the tumor is diagnosed, and the degree to which the tumor has spread at the time of diagnosis, are different for children with birth defects and children without birth defects. This study attempts to answer these important questions. By doing so, it may help scientists and physicians to understand the causes of cancer in children with birth defects and diagnose cancer at earlier stages when it is more treatable.
出生缺陷是儿童癌症已明确的风险因素。尽管如此,出生缺陷患儿的癌症流行病学特征仍未得到充分描述。
利用美国4个州基于人群的登记处数据,本研究将患癌症但无出生缺陷的儿童(n = 13111)与患癌症且有1种或更多非综合征性出生缺陷的儿童(n = 1616)进行了比较。目的是评估癌症诊断特征,包括肿瘤类型、诊断时年龄和诊断时分期。
与患癌症儿童的总体人群相比,有出生缺陷的儿童被诊断出更多的胚胎性肿瘤(26.6%对18.7%;q < 0.001),包括神经母细胞瘤(12.5%对8.2%;q < 0.001)和肝母细胞瘤(5.0%对1.3%;q < 0.001),但血液系统恶性肿瘤较少,包括急性淋巴细胞白血病(12.4%对24.4%;q < 0.001)。在按年龄分层的分析中,肿瘤类型的差异在1岁以下儿童和1至4岁儿童中很明显,但在5岁及以上儿童中减弱。对于大多数癌症,包括白血病、淋巴瘤、星形细胞瘤、髓母细胞瘤、室管膜瘤、胚胎性肿瘤和生殖细胞肿瘤,有出生缺陷的儿童诊断时年龄更小(所有q < 0.05)。
结果表明出生缺陷患儿可能存在病因异质性,对未来的监测工作有影响,并增加了出生缺陷患儿癌症确诊存在差异的可能性。
科学研究表明,有出生缺陷的儿童患癌症的风险增加。然而,这些研究未能确定重要的肿瘤特征,如诊断出的肿瘤类型、诊断肿瘤时的年龄以及诊断时肿瘤扩散的程度,对于有出生缺陷的儿童和无出生缺陷的儿童是否不同。本研究试图回答这些重要问题。这样做可能有助于科学家和医生了解有出生缺陷儿童患癌症的原因,并在癌症更易治疗的早期阶段进行诊断。