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2000 - 2017年美国松果体母细胞瘤的流行病学

Epidemiology of pineoblastoma in the United States, 2000-2017.

作者信息

Greppin Kaitlyn, Cioffi Gino, Waite Kristin A, Ostrom Quinn T, Landi Daniel, Takaoka Kailey, Kruchko Carol, Barnholtz-Sloan Jill S

机构信息

Hathaway Brown School, Science Research & Engineering Program, Shaker Heights, Ohio, USA.

Trans Divisional Research Program (TDRP), Division of Cancer Epidemiology and Genetics (DCEG), National Cancer Institute, Bethesda, Maryland, USA.

出版信息

Neurooncol Pract. 2022 Jan 27;9(2):149-157. doi: 10.1093/nop/npac009. eCollection 2022 Apr.


DOI:10.1093/nop/npac009
PMID:35371520
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8965073/
Abstract

BACKGROUND: Pineoblastoma (PB) is a rare malignant brain tumor originating in the pineal gland. Here, we provide a comprehensive epidemiological analysis of PB in the United States from 2000 to 2017. METHODS: Data on 1133 patients with PB were acquired from the Central Brain Tumor Registry of the United States, in collaboration with the Centers for Disease Control and Prevention and the National Cancer Institute, from 2000 to 2017. Age-adjusted incidence rates (AAIRs) per 100 000 and incidence rate ratios (IRRs) were reported for age, sex, race, and ethnicity. Using the National Program of Cancer Registries survival database, median survival and hazard ratios (HRs) were evaluated for overall survival from 2001 to 2016. RESULTS: Incidence was highest in ages 0-4 years (AAIR: 0.049, 95% CI: 0.042-0.056), decreasing as age increased. Incidence was higher among patients who are Black compared to patients who are White (IRR: 1.71, 95% CI: 1.48-1.98, < .001), and was impacted by age at diagnosis, with Black-to-White incidence highest in children ages 5-9 years (IRR: 3.43, 95% CI: 2.36-4.94, < .001). Overall survival was lower for males (HR: 1.39, 95% CI: 1.07-1.79, = .013). All age groups, excluding those over 40, had improved survival compared to ages 0-4 years. Those who received surgical intervention had better survival compared to those who did not receive surgical treatment. CONCLUSION: PB incidence is highest among children and patients who are Black, and there may be a potential interaction between these factors. Survival is worse among males, young children, and elderly adults, and those who received no surgery. Comprehensive, population-based statistics provide critical information on PB characteristics that could be useful in impacting patient care and prognosis.

摘要

背景:松果体母细胞瘤(PB)是一种起源于松果体的罕见恶性脑肿瘤。在此,我们对2000年至2017年美国的松果体母细胞瘤进行了全面的流行病学分析。 方法:与疾病控制和预防中心以及国家癌症研究所合作,从美国中央脑肿瘤登记处获取了2000年至2017年1133例松果体母细胞瘤患者的数据。报告了每10万人的年龄调整发病率(AAIRs)以及年龄、性别、种族和民族的发病率比(IRRs)。使用国家癌症登记项目生存数据库,评估了2001年至2016年总体生存的中位生存期和风险比(HRs)。 结果:发病率在0 - 4岁年龄组最高(AAIR:0.049,95%CI:0.042 - 0.056),随年龄增长而降低。黑人患者的发病率高于白人患者(IRR:1.71,95%CI:1.48 - 1.98,P <.001),且受诊断年龄的影响,5 - 9岁儿童中黑人与白人的发病率差异最大(IRR:3.43,95%CI:2.36 - 4.94,P <.001)。男性的总体生存率较低(HR:1.39,95%CI:1.07 - 1.79,P = 0.013)。除40岁以上年龄组外,所有年龄组的生存率均高于0 - 4岁年龄组。接受手术干预的患者生存率高于未接受手术治疗的患者。 结论:松果体母细胞瘤的发病率在儿童和黑人患者中最高,这些因素之间可能存在潜在的相互作用。男性、幼儿和老年人以及未接受手术的患者生存率较差。基于人群的综合统计数据提供了有关松果体母细胞瘤特征的关键信息,这可能有助于影响患者护理和预后。

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引用本文的文献

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Development and Validation of Survival Prediction Models for Patients With Pineoblastomas Using Deep Learning: A SEER-Based Study.

Cancer Rep (Hoboken). 2025-8

[2]
An aggressive, unresected pineoblastoma in an adult woman: the role of exclusive radiotherapy - a case report and literature review.

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[3]
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Radiol Case Rep. 2025-3-27

[4]
Recent Advances in Pineoblastoma Research: Molecular Classification, Modelling and Targetable Vulnerabilities.

Cancers (Basel). 2025-2-20

[5]
Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition.

Clin Cancer Res. 2025-4-14

[6]
Pediatric diencephalic tumors: a constellation of entities and management modalities.

Front Oncol. 2023-7-13

[7]
Post-Surgical Prognosis of Patients with Pineoblastoma: A Systematic Review and Individual Patient Data Analysis with Trends over Time.

Cancers (Basel). 2023-6-27

[8]
Histopathology and molecular pathology of pediatric pineal parenchymal tumors.

Childs Nerv Syst. 2023-9

本文引用的文献

[1]
CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2013-2017.

Neuro Oncol. 2020-10-30

[2]
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Cancer Epidemiol Biomarkers Prev. 2020-7

[3]
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Neurosurgery. 2020-5-1

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Acta Neuropathol. 2020-2

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Molecular subgrouping of primary pineal parenchymal tumors reveals distinct subtypes correlated with clinical parameters and genetic alterations.

Acta Neuropathol. 2020-2

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World Neurosurg. 2018-10

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World Neurosurg. 2014-12

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Cancer. 2011-6-29

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