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颅脊柱放疗治疗小儿转移性低度胶质瘤。

Craniospinal irradiation for treatment of metastatic pediatric low-grade glioma.

机构信息

Department of Radiation Oncology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, MS 210, Memphis, TN, 38105, USA.

Department of Radiation Oncology, Cleveland Clinic, Cleveland, OH, USA.

出版信息

J Neurooncol. 2017 Sep;134(2):317-324. doi: 10.1007/s11060-017-2525-6. Epub 2017 Jun 17.

Abstract

Patients with disseminated pediatric low-grade glioma (LGG) initially treated with chemotherapy frequently experience disease progression, with 5-year event-free survival (EFS) of <20% and 10-year overall survival (OS) of approximately 70%. This study aimed to describe outcomes of metastatic pediatric LGG treated with craniospinal irradiation (CSI). A retrospective study was performed of all patients with metastatic pediatric LGG treated with CSI at a single institution. EFS was defined as survival without disease progression or secondary high-grade glioma. Dates were counted from the first day of irradiation. We identified 12 eligible patients; all had histologically confirmed LGG. Metastatic disease was present at initial presentation in 9 patients. The median age at CSI was 9.3 years. The 5-year EFS and OS were 71% (95% CI 33.7-89.5) and 70% (95% CI 32.9-89.2), respectively. No deaths were observed among the patients who underwent subtotal resection (STR) before radiotherapy, whereas 3 patients who had undergone biopsy died (OS log-rank P = 0.01). EFS may be longer among patients who underwent STR before RT (EFS log-rank P = 0.03), with a hazard ratio for biopsy of 8.4 (vs. STR; 95% CI 0.8-84.0, P = 0.07). No patient experienced acute toxicity of grade 3 or higher. Patients with metastatic pediatric LGG treated with CSI experienced longer EFS than historical cohorts treated with chemotherapy alone, with similar OS. CSI may be considered in the management of metastatic pediatric LGG, particularly in older children experiencing progression after chemotherapy.

摘要

患有播散性儿科低级别胶质瘤 (LGG) 的患者最初接受化疗治疗,常出现疾病进展,5 年无事件生存率 (EFS) <20%,10 年总生存率 (OS) 约为 70%。本研究旨在描述接受颅脊髓照射 (CSI) 治疗的转移性儿科 LGG 患者的结局。对在单一机构接受 CSI 治疗的所有转移性儿科 LGG 患者进行了回顾性研究。EFS 定义为无疾病进展或继发性高级别胶质瘤的生存。日期从照射的第一天开始计算。我们确定了 12 名符合条件的患者;所有患者均经组织学证实为 LGG。9 名患者在初次就诊时即存在转移性疾病。CSI 时的中位年龄为 9.3 岁。5 年 EFS 和 OS 分别为 71%(95%CI 33.7-89.5)和 70%(95%CI 32.9-89.2)。在接受放疗前进行部分切除术 (STR) 的患者中没有观察到死亡,而在接受活检的 3 例患者中观察到死亡(OS 对数秩检验 P=0.01)。在接受 STR 治疗的患者中,EFS 可能更长(EFS 对数秩检验 P=0.03),活检的风险比为 8.4(STR;95%CI 0.8-84.0,P=0.07)。没有患者发生 3 级或更高级别的急性毒性。接受 CSI 治疗的转移性儿科 LGG 患者的 EFS 长于单独接受化疗治疗的历史队列,OS 相似。CSI 可考虑用于治疗转移性儿科 LGG,特别是在化疗后进展的年龄较大的儿童。

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