Dressler Emily V, Dolecek Therese A, Liu Meng, Villano John L
Division of Cancer Biostatistics (EVD, ML) and Departments of Medicine and Neurology (JLV), University of Kentucky, 800 Rose St., CC446, Lexington, KY, 40536-0093, USA.
Division of Epidemiology and Biostatistics and Institute for Health Research and Policy, School of Public Health (TAD), University of Illinois at Chicago, Chicago, IL, USA.
J Neurooncol. 2017 May;132(3):497-506. doi: 10.1007/s11060-017-2400-5. Epub 2017 Mar 13.
We evaluated the American College of Surgeon's National Cancer Data Base (NCDB) to describe current hospital-based epidemiologic frequency, survival, and patterns of care of pediatric medulloblastoma. We analyzed NCDB 1998-2011 data on medulloblastoma for children ages 0-19 years using logistic and poisson regression, Kaplan-Meier survival estimates, and Cox proportional hazards models. 3647 cases of medulloblastoma in those aged 0-19 years were identified. Chemotherapy was received by 79 and 74% received radiation, with 65% receiving both therapies. Those who received radiation were more likely to be older than four, while those who received chemotherapy were more likely to be age four and younger. Variables associated with receipt of neither radiation nor chemotherapy included age at diagnosis of <1 year, female gender, being of race other than black or white, having no insurance, and living in a residential area with a low level of high school graduates. Better overall survival was observed as age at diagnosis increased, in females, and having received radiation. Compared to medulloblastoma, NOS, better survival was observed for those with demoplastic medulloblastoma, with worse survival in those with large cell medulloblastoma. Majority received multi- disciplinary therapy and radiation had the greatest effect on survival. Ages four and under were most likely to receive chemotherapy and least likely to receive radiation. Suboptimal treatment included 17.8% that did not receive chemotherapy, of which 11.8% received neither chemotherapy nor radiation. Disparities associated with medical access were characteristics for not receiving standard treatment, which resulted in poor outcome.
我们评估了美国外科医师学会的国家癌症数据库(NCDB),以描述当前基于医院的小儿髓母细胞瘤的流行病学频率、生存率和治疗模式。我们使用逻辑回归和泊松回归、Kaplan-Meier生存估计以及Cox比例风险模型,分析了NCDB中1998 - 2011年0至19岁儿童髓母细胞瘤的数据。共识别出3647例0至19岁的髓母细胞瘤病例。79%的患者接受了化疗,74%接受了放疗,65%同时接受了两种治疗。接受放疗的患者更可能年龄大于4岁,而接受化疗的患者更可能年龄为4岁及以下。与既未接受放疗也未接受化疗相关的变量包括诊断时年龄<1岁、女性、非黑种人或白种人、没有保险以及居住在高中毕业生水平较低的居民区。随着诊断时年龄增加、女性以及接受了放疗,总体生存率更高。与髓母细胞瘤,NOS相比,促结缔组织增生性髓母细胞瘤患者的生存率更好,而大细胞髓母细胞瘤患者的生存率更差。大多数患者接受了多学科治疗,放疗对生存率的影响最大。4岁及以下的儿童最有可能接受化疗,最不可能接受放疗。次优治疗包括17.8%未接受化疗的患者,其中11.8%既未接受化疗也未接受放疗。与医疗可及性相关的差异是未接受标准治疗的特征,这导致了不良结局。