From the Department of Neurology (B.M.A., C.M.), New York Presbyterian/Weill Cornell Medicine and Memorial Sloan Kettering Cancer Center; and Departments of Radiology (V.H.) and Neurology (L.M.D., A.M.M.) Memorial Sloan Kettering Cancer Center, New York, NY.
Neurology. 2019 May 21;92(21):e2483-e2491. doi: 10.1212/WNL.0000000000007529. Epub 2019 Apr 24.
To perform a retrospective analysis examining the incidence and prognosis of glioma patients with leptomeningeal disease (LMD) at Memorial Sloan Kettering Cancer Center over a 15-year period and correlate these findings with clinicopathologic characteristics.
We conducted a retrospective review of glioma patients with LMD at Memorial Sloan Kettering Cancer Center diagnosed from 2001 to 2016. Patients were identified through a keyword search of their electronic medical record and by ICD-9 codes.
One hundred three patients were identified with disseminated LMD and 85 patients with subependymal spread of disease, 4.7% of all patients with glioma. These cohorts were analyzed separately for time to development of disseminated LMD/subependymal LMD, median overall survival, and survival from LMD diagnosis. Patients were pooled for subsequent analyses (n = 188) because of comparable clinical behavior. LMD was present at glioma diagnosis in 10% of patients. In the remaining 90% of patients diagnosed at recurrence, time to LMD diagnosis, survival after LMD diagnosis, and overall survival varied by original histology. Patients with oligodendroglioma had a median survival of 10.8 (range 1.8-67.7) months, astrocytoma 6.5 (0.1-28.5) months, and glioblastoma 3.8 (0.1-32.6) months after LMD diagnosis. In addition, we found that treatment of LMD was associated with superior performance status and increased survival.
Patients with LMD diagnosed at relapse may not have decreased overall survival as compared to historical controls with parenchymal relapse and may benefit from treatment.
对纪念斯隆-凯特琳癌症中心(Memorial Sloan Kettering Cancer Center) 15 年来患有神经胶质瘤性脑膜疾病(LMD)的患者的发病率和预后进行回顾性分析,并将这些发现与临床病理特征相关联。
我们对 2001 年至 2016 年在 Memorial Sloan Kettering Cancer Center 确诊的患有 LMD 的神经胶质瘤患者进行了回顾性研究。通过电子病历的关键字搜索和 ICD-9 代码来识别患者。
103 例患者被诊断为弥漫性 LMD,85 例患者为室管膜下播散,占所有神经胶质瘤患者的 4.7%。分别分析了这两个队列的 LMD 发展时间、中位总生存期和 LMD 诊断后的生存期。由于临床行为相似,将患者合并进行后续分析(n=188)。10%的患者在神经胶质瘤诊断时即存在 LMD。在其余 90%在复发时诊断的患者中,LMD 的诊断时间、LMD 诊断后的生存时间和总生存时间因原始组织学而异。少突胶质细胞瘤患者的中位生存时间为 10.8 个月(范围 1.8-67.7),星形细胞瘤为 6.5 个月(0.1-28.5),胶质母细胞瘤为 3.8 个月(0.1-32.6)。此外,我们发现 LMD 的治疗与更好的表现状态和生存延长相关。
与具有实质复发的历史对照相比,在复发时诊断出 LMD 的患者的总生存时间可能不会降低,并且可能受益于治疗。