Department of Medicine, Section of Epidemiology and Population Sciences, Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas, USA.
Unit of Epidemiology, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Neuro Oncol. 2019 Nov 4;21(11):1357-1375. doi: 10.1093/neuonc/noz123.
Primary brain tumors account for ~1% of new cancer cases and ~2% of cancer deaths in the United States; however, they are the most commonly occurring solid tumors in children. These tumors are very heterogeneous and can be broadly classified into malignant and benign (or non-malignant), and specific histologies vary in frequency by age, sex, and race/ethnicity. Epidemiological studies have explored numerous potential risk factors, and thus far the only validated associations for brain tumors are ionizing radiation (which increases risk in both adults and children) and history of allergies (which decreases risk in adults). Studies of genetic risk factors have identified 32 germline variants associated with increased risk for these tumors in adults (25 in glioma, 2 in meningioma, 3 in pituitary adenoma, and 2 in primary CNS lymphoma), and further studies are currently under way for other histologic subtypes, as well as for various childhood brain tumors. While identifying risk factors for these tumors is difficult due to their rarity, many existing datasets can be leveraged for future discoveries in multi-institutional collaborations. Many institutions are continuing to develop large clinical databases including pre-diagnostic risk factor data, and developments in molecular characterization of tumor subtypes continue to allow for investigation of more refined phenotypes. Key Point 1. Brain tumors are a heterogeneous group of tumors that vary significantly in incidence by age, sex, and race/ethnicity.2. The only well-validated risk factors for brain tumors are ionizing radiation (which increases risk in adults and children) and history of allergies (which decreases risk).3. Genome-wide association studies have identified 32 histology-specific inherited genetic variants associated with increased risk of these tumors.
原发性脑肿瘤约占美国新发癌症病例的 1%和癌症死亡人数的 2%;然而,它们是儿童中最常见的实体肿瘤。这些肿瘤非常异质,可以广泛分为恶性和良性(或非恶性),特定的组织学在年龄、性别和种族/民族方面的频率不同。流行病学研究已经探讨了许多潜在的风险因素,迄今为止,唯一与脑肿瘤相关的验证关联是电离辐射(在成人和儿童中都增加风险)和过敏史(在成人中降低风险)。遗传风险因素的研究已经确定了 32 个种系变异与这些肿瘤在成人中的风险增加相关(25 个在神经胶质瘤、2 个在脑膜瘤、3 个在垂体腺瘤和 2 个在原发性中枢神经系统淋巴瘤),目前正在对其他组织学亚型以及各种儿童脑肿瘤进行进一步研究。由于这些肿瘤的罕见性,确定其风险因素具有挑战性,但许多现有的数据集可以在多机构合作中为未来的发现提供支持。许多机构正在继续开发大型临床数据库,包括预诊断风险因素数据,并且肿瘤亚型的分子特征的发展继续允许对更精细的表型进行研究。要点 1. 脑肿瘤是一组异质性肿瘤,其发病率在年龄、性别和种族/民族方面差异很大。2. 唯一经过充分验证的脑肿瘤风险因素是电离辐射(在成人和儿童中都增加风险)和过敏史(降低风险)。3. 全基因组关联研究已经确定了 32 个与这些肿瘤风险增加相关的特定组织学遗传变异。