1 St Jude Children's Research Hospital, Memphis, TN.
2 Children's Hospitals and Clinics of Minnesota, Minneapolis, MN.
J Clin Oncol. 2019 Apr 20;37(12):974-983. doi: 10.1200/JCO.18.01765. Epub 2019 Feb 27.
The Children's Oncology Group trial ACNS0121 estimated event-free survival (EFS) and overall survival for children with intracranial ependymoma treated with surgery, radiation therapy, and-selectively-with chemotherapy. Treatment was administered according to tumor location, histologic grade, and extent of resection. The impacts of histologic grade, focal copy number gain on chromosome 1q, and DNA methylation profiles were studied for those undergoing surgery and immediate postoperative conformal radiation therapy (CRT).
ACNS0121 included 356 newly diagnosed patients (ages 1 to 21 years). Patients with classic supratentorial ependymoma were observed after gross total resection (GTR). Those undergoing subtotal resection received chemotherapy, second surgery, and CRT. The remaining patients received immediate postoperative CRT after near-total resection or GTR. CRT was administered with a 1.0-cm clinical target volume margin. The cumulative total dose was 59.4 Gy, except for patients who underwent GTR and were younger than age 18 months (who received 54 Gy). Patients were enrolled between October 2003 and September 2007 and were observed for 5 years. Supratentorial tumors were evaluated for fusion; infratentorial tumors, for chromosome 1q gain. Classification of posterior fossa groups A and B was made by methylation profiles.
The 5-year EFS rates were 61.4% (95% CI, 34.5% to 89.6%), 37.2% (95% CI, 24.8% to 49.6%), and 68.5% (95% CI, 62.8% to 74.2%) for observation, subtotal resection, and near-total resection/GTR groups given immediate postoperative CRT, respectively. The 5-year EFS rates differed significantly by tumor grade ( = .0044) but not by age, location, fusion status, or posterior fossa A/posterior fossa B grouping. EFS was higher for patients with infratentorial tumors without 1q gain than with 1q gain (82.8% [95% CI, 74.4% to 91.2%] 47.4% [95% CI, 26.0% to 68.8%]; = .0013).
The EFS for patients with ependymoma younger than 3 years of age who received immediate postoperative CRT and for older patients is similar. Irradiation should remain the mainstay of care for most subtypes.
儿童肿瘤协作组试验 ACNS0121 评估了接受手术、放疗和-选择性-化疗治疗的颅内室管膜瘤儿童的无事件生存(EFS)和总生存。治疗根据肿瘤位置、组织学分级和切除范围进行。对接受手术和术后即刻适形放疗(CRT)的患者进行了组织学分级、1q 染色体焦点拷贝数增益和 DNA 甲基化谱的影响研究。
ACNS0121 纳入了 356 例新诊断的患者(年龄 1 至 21 岁)。经典幕上室管膜瘤患者在大体全切除(GTR)后观察。接受次全切除的患者接受化疗、二次手术和 CRT。其余患者在近全切除或 GTR 后立即接受术后 CRT。CRT 采用 1.0cm 的临床靶区边界。累积总剂量为 59.4Gy,年龄小于 18 个月且接受 GTR 的患者除外(他们接受 54Gy)。患者于 2003 年 10 月至 2007 年 9 月入组,并观察 5 年。幕上肿瘤评估融合;后颅窝肿瘤评估 1q 增益。通过甲基化谱对后颅窝 A、B 组进行分类。
接受术后即刻 CRT 的观察、次全切除和近全切除/GTR 组的 5 年 EFS 率分别为 61.4%(95%CI,34.5%至 89.6%)、37.2%(95%CI,24.8%至 49.6%)和 68.5%(95%CI,62.8%至 74.2%)。肿瘤分级( =.0044)差异有统计学意义,但年龄、位置、融合状态或后颅窝 A/后颅窝 B 分组差异无统计学意义。无 1q 增益的幕下肿瘤患者的 EFS 高于有 1q 增益的患者(82.8%[95%CI,74.4%至 91.2%]比 47.4%[95%CI,26.0%至 68.8%]; =.0013)。
接受术后即刻 CRT 的 3 岁以下和年龄较大的室管膜瘤患者的 EFS 相似。放疗仍应是大多数亚型的主要治疗方法。