Main Caroline, Wilson Jayne S, Stevens Simon P, Houlton Aimee E, English Martin, Kearns Pamela R, Phillips Bob, Pizer Barry, Wilne Sophie, Wheatley Keith
Cancer Research UK Clinical Trials Unit (CRCTU), Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.
Birmingham Children's Hospital NHS Foundation Trust, Birmingham, UK.
Syst Rev. 2015 Nov 20;4:168. doi: 10.1186/s13643-015-0155-7.
The objective of the study is to conduct a systematic review to compare the effects of high-dose chemotherapy (HDCT) with autologous haematopoietic stem cell transplantation (HSCT) versus standard-dose chemotherapy (SDCT) in children with malignant central nervous system (CNS) tumours.
Standard systematic review methods aimed at minimising bias will be employed for study identification, selection and data extraction. Ten electronic databases will be searched, along with citation searching and reference checking. Studies assessing the effects of HDCT with HSCT in children with CNS tumours will be included. The outcomes are survival (overall, progression-free, event-free, disease-free), response rates, short- and long-term adverse events and health-related quality of life (HRQoL). Two reviewers will independently screen and select randomised and non-randomised controlled trials and controlled and uncontrolled observational studies for inclusion. Quality assessment will be tailored to the different study designs. Where possible data will be summarised using combined estimates of effect for the hazard ratio for survival outcomes and the risk ratio for response rates. A fixed effect model will be used; sub-group analyses and meta-regression will be used to explore potential sources of heterogeneity between studies.
Given the poor prognosis of malignant brain tumours in children in terms of survival and quality of life, this review will help guide clinical practice by summarising the current evidence on the use of high-dose myeloblative chemotherapy with stem cell support in children with CNS tumours.
本研究的目的是进行一项系统评价,比较大剂量化疗(HDCT)联合自体造血干细胞移植(HSCT)与标准剂量化疗(SDCT)对儿童恶性中枢神经系统(CNS)肿瘤的疗效。
将采用旨在尽量减少偏倚的标准系统评价方法进行研究识别、选择和数据提取。将检索十个电子数据库,并进行引文检索和参考文献核对。纳入评估HDCT联合HSCT对CNS肿瘤患儿疗效的研究。结局指标包括生存率(总生存率、无进展生存率、无事件生存率、无病生存率)、缓解率、短期和长期不良事件以及健康相关生活质量(HRQoL)。两名评价者将独立筛选并选择随机和非随机对照试验以及对照和非对照观察性研究纳入。质量评估将根据不同的研究设计进行调整。可能的话,将使用生存结局风险比和缓解率风险比的合并效应估计值来汇总数据。将使用固定效应模型;亚组分析和meta回归将用于探索研究之间潜在的异质性来源。
鉴于儿童恶性脑肿瘤在生存和生活质量方面预后较差,本评价将通过总结目前关于大剂量清髓性化疗联合干细胞支持治疗CNS肿瘤患儿的证据,帮助指导临床实践。