Division of Hematology/Oncology, Department of Pediatrics, University of California, San Francisco, 550 16th Street, 4th Floor, San Francisco, CA, 94158, USA.
Department of Neurology, University of California, San Francisco, 550 Sandler Neurosciences, 625 Nelson Rising Lane, 402B, Box 0434, San Francisco, CA, 94158, USA.
J Neurooncol. 2018 Mar;137(1):103-110. doi: 10.1007/s11060-017-2701-8. Epub 2017 Dec 4.
Recurrent pediatric high-grade glioma is a leading cause of cancer-related death in children. We report results of a systematic review and meta-analysis investigating survival outcome in pediatric patients with recurrent high-grade glioma over the last 20 years. MEDLINE/PubMed, EMBASE, Web of Science and Cochrane Review databases were searched for relevant studies reporting on survival outcomes for pediatric patients with recurrent high-grade glioma treated between 1996 and 2016. Progression-free survival (PFS) and overall survival (OS) were calculated cumulatively over all studies, by therapy subgroup, and by decade of treatment. Random effects models were used to control for heterogeneity as measured by the I statistic. A total of 17 studies across 4 treatment strategies were included. Eleven investigated traditional chemotherapy, 1 investigated targeted therapy, 3 investigated immunotherapy, and 2 investigated radiotherapy. A total of 129 patients were included with a median age of 10.0 years. Cumulative PFS was 3.5 months (95% CI 2.1-5.0). Cumulative OS was 5.6 months (95% CI 3.9-7.3). OS was 4.0 months (95% CI 1.9-6.1) using traditional chemotherapy, 9.3 months using targeted therapies (95% CI 5.4-13), 6.9 months using immunotherapy (95% CI 2.1-12), and 14 months using reirradiation (95% CI 2.8-25). OS between 1996 and 2006 was 4.2 months (95% CI 2.1-6.2) compared to 8.5 months (95% CI 5.6-11) after 2006. Pediatric patients with recurrent high-grade glioma suffer from poor PFS and OS, regardless of therapy. There may be a trend towards improved OS in the last decade.
复发性小儿高级别胶质瘤是儿童癌症相关死亡的主要原因。我们报告了一项系统评价和荟萃分析的结果,该研究调查了过去 20 年来接受治疗的复发性高级别脑胶质瘤患儿的生存结果。在 MEDLINE/PubMed、EMBASE、Web of Science 和 Cochrane Review 数据库中,检索了 1996 年至 2016 年间发表的关于复发性高级别脑胶质瘤患儿治疗后生存结果的相关研究。通过治疗亚组和治疗年代,对所有研究的无进展生存期(PFS)和总生存期(OS)进行累积计算。使用随机效应模型控制异质性,以 I 统计量衡量。共有 4 种治疗策略的 17 项研究纳入分析。其中 11 项研究调查了传统化疗,1 项研究调查了靶向治疗,3 项研究调查了免疫治疗,2 项研究调查了放射治疗。共纳入 129 例患者,中位年龄为 10.0 岁。累积 PFS 为 3.5 个月(95%CI 2.1-5.0)。累积 OS 为 5.6 个月(95%CI 3.9-7.3)。使用传统化疗的 OS 为 4.0 个月(95%CI 1.9-6.1),使用靶向治疗的 OS 为 9.3 个月(95%CI 5.4-13),使用免疫治疗的 OS 为 6.9 个月(95%CI 2.1-12),使用再放疗的 OS 为 14 个月(95%CI 2.8-25)。1996 年至 2006 年的 OS 为 4.2 个月(95%CI 2.1-6.2),而 2006 年后的 OS 为 8.5 个月(95%CI 5.6-11)。复发性高级别脑胶质瘤患儿无论采用何种治疗方法,PFS 和 OS 均较差。在过去的十年中,OS 可能有改善的趋势。