Chennakesavalu Mohansrinivas, Pudela Caileigh, Applebaum Mark A, Lee Sang Mee, Che Yan, Naranjo Arlene, Park Julie R, Volchenboum Samuel L, Henderson Tara O, Cohn Susan L, Desai Ami V
Pritzker School of Medicine, University of Chicago, Chicago, IL, USA.
MedStar Georgetown University Hospital, Washington, D.C., USA.
EJC Paediatr Oncol. 2023 Dec;2. doi: 10.1016/j.ejcped.2023.100022. Epub 2023 Jul 20.
Racial/ethnic survival disparities in neuroblastoma were first reported more than a decade ago. We sought to investigate if these disparities have persisted with current era therapy.
Two patient cohorts were identified in the International Neuroblastoma Risk Group Data Commons (INRGdc) (Cohort 1: diagnosed 2001-2009, n=4359; Cohort 2: diagnosed 2010-2019, n=4891). Chi-squared tests were used to assess the relationship between race/ethnicity and clinical and biologic features. Survival was estimated by the Kaplan-Meier method. Cox proportional hazards regression analyses were performed to investigate the association between racial/ethnic groups and prognostic markers.
Significantly higher 5-year event-free survival (EFS) and overall survival (OS) were observed for Cohort 2 compared to Cohort 1 (P<0.001 and P<0.001, respectively). Compared to White patients, Black patients in both cohorts had a higher proportion of high-risk disease (Cohort 1: P<0.001; Cohort 2: P<0.001) and worse EFS (Cohort 1: P<0.001; Cohort 2 P<0.001) and OS (Cohort 1: P<0.001; Cohort 2: P<0.001). In Cohort 1, Native Americans also had a higher proportion of high-risk disease (P=0.03) and inferior EFS/OS. No significant survival disparities were observed for low- or intermediate-risk patients in either cohort or high-risk patients in Cohort 1. Hispanic patients with high-risk disease in Cohort 2 had significantly inferior OS (P=0.047). Significantly worse OS, but not EFS, (P=0.006 and P=0.02, respectively) was also observed among Black and Hispanic patients assigned to receive post-Consolidation dinutuximab on clinical trials (n=885).
Racial/ethnic survival disparities have persisted over time and were observed among high-risk patients assigned to receive post-Consolidation dinutuximab.
十多年前首次报道了神经母细胞瘤患者在种族/族裔方面的生存差异。我们试图研究在当前时代的治疗下这些差异是否仍然存在。
在国际神经母细胞瘤风险组数据共享库(INRGdc)中确定了两个患者队列(队列1:2001 - 2009年诊断,n = 4359;队列2:2010 - 2019年诊断,n = 4891)。采用卡方检验评估种族/族裔与临床和生物学特征之间的关系。通过Kaplan-Meier方法估计生存率。进行Cox比例风险回归分析以研究种族/族裔群体与预后标志物之间的关联。
与队列1相比,队列2观察到显著更高的5年无事件生存率(EFS)和总生存率(OS)(分别为P < 0.001和P < 0.001)。与白人患者相比,两个队列中的黑人患者高危疾病比例更高(队列1:P < 0.001;队列2:P < 0.001),EFS更差(队列1:P < 0.001;队列2:P < 0.001),OS也更差(队列1:P < 0.001;队列2:P < 0.001)。在队列1中,美国原住民的高危疾病比例也更高(P = 0.03),EFS/OS较差。在两个队列中的低风险或中风险患者或队列1中的高风险患者中未观察到显著的生存差异。队列2中患有高危疾病的西班牙裔患者的OS显著较差(P = 0.047)。在临床试验中被分配接受巩固治疗后使用地努图希单抗的黑人和西班牙裔患者中也观察到OS显著更差,但EFS没有(分别为P = 0.006和P = 0.02)(n = 885)。
种族/族裔生存差异长期存在,并且在被分配接受巩固治疗后使用地努图希单抗的高风险患者中也观察到了这种差异。