Department of Neurological Surgery, University of Miami, Miami, FL, United States.
Department of Neurological Surgery, University of Miami, Miami, FL, United States.
Clin Neurol Neurosurg. 2022 Jul;218:107265. doi: 10.1016/j.clineuro.2022.107265. Epub 2022 Apr 30.
Diffuse leptomeningeal glioneuronal tumor (DLGNT), also known as oligodendrogliomatosis, is a rare neuro-oncologic condition along the neuraxis that remains poorly understood in children. We sought to describe our institutional experience and quantitively summarize the clinical survival and prognostic features of DLGNT in the pediatric population across the contemporary literature.
We report four institutional cases of pediatric DLGNT diagnosed between 2000 and 2020 based on retrospective review of our records, and performed a comprehensive literature search for published cases from 2000 onwards to create an integrated cohort for analysis. Kaplan-Meier estimations, Fisher's exact test, and logistic regression were utilized to interrogate the data.
Of our four cases, three females aged 2-, 3- and 13-years old at diagnosis survived 6-years, 3-years and 14-months respectively, and one male aged 5-years old at diagnosis was still alive 5 years later. Our overall integrated cohort consisted of 54 pediatric DLGNT patients, with 19 (35%) female and 35 (65%) male patients diagnosed at an average age of 6.4 years (range, 1.3-17 years) by means of surgical biopsy. Chemotherapy was used in 45 cases (83%), and mean follow-up time of 54 months (range, 3-204). Across the entire cohort, overall survival 1 month after diagnosis was 96% (95% CI 86-99%), and by 10 years was 69% (95% CI 49-82%). On multivariate analysis of complete data, chemotherapy treatment (HR=0.23, P = 0.04) was statistically predictive of longer overall survival.
More than 2-out-of-3 pediatric DLGNT patients survive beyond one decade. Chemotherapy is statistically associated with longer survival in DLGNT pediatric patients and should form the core of any treatment regimen in this setting. Early detection by means of judicious imaging and surgical biopsy for tissue diagnosis can lead to earlier treatment and likely superior outcomes.
弥漫性软脑膜胶质神经元肿瘤(DLGNT),也称为少突胶质细胞瘤病,是一种沿神经轴罕见的神经肿瘤疾病,在儿童中仍知之甚少。我们旨在描述我们机构的经验,并在当代文献中定量总结儿科人群中 DLGNT 的临床生存和预后特征。
我们根据病历回顾报告了 2000 年至 2020 年期间诊断的 4 例机构内儿童 DLGNT 病例,并对 2000 年以后发表的病例进行了全面的文献检索,以创建一个综合队列进行分析。利用 Kaplan-Meier 估计、Fisher 确切检验和逻辑回归来研究数据。
我们的 4 例病例中,3 例女性患者的年龄分别为 2 岁、3 岁和 13 岁,生存时间分别为 6 年、3 年和 14 个月,1 例 5 岁的男性患者在诊断后 5 年仍存活。我们的综合队列由 54 例儿科 DLGNT 患者组成,其中 19 例(35%)为女性,35 例(65%)为男性,平均诊断年龄为 6.4 岁(范围 1.3-17 岁),通过手术活检确诊。45 例(83%)患者接受了化疗,平均随访时间为 54 个月(范围 3-204 个月)。在整个队列中,诊断后 1 个月的总生存率为 96%(95%CI 86%-99%),10 年生存率为 69%(95%CI 49%-82%)。在完整数据的多变量分析中,化疗治疗(HR=0.23,P=0.04)与更长的总生存时间具有统计学相关性。
超过 2/3 的儿科 DLGNT 患者可存活 10 年以上。化疗与 DLGNT 儿科患者的生存时间延长具有统计学相关性,并且应该成为该治疗环境中任何治疗方案的核心。通过明智的影像学和手术活检进行早期检测以进行组织诊断,可以更早地进行治疗并可能获得更好的结果。