Department of Pediatric Surgery, Liaocheng People's Hospital, Shandong, PR China.
Medicine (Baltimore). 2021 Dec 10;100(49):e28096. doi: 10.1097/MD.0000000000028096.
Neuroblastoma is a common solid malignant tumor in children. Despite the development of new treatment options, the prognosis of high-risk neuroblastoma patients is still poor. High-dose chemotherapy and hematopoietic stem cell (HSC) transplantation might improve survival of patients with refractory neuroblastoma. In this study, we aimed to summarize the efficacy of autologous or allogeneic HSC transplantation combined with high-dose chemotherapy for patients with refractory neuroblastoma through the meta-analysis.
Relevant clinical trials of autologous or allogeneic HSC transplantation for the treatment refractory neuroblastoma patients will be searched in Web of Science, Cochrane Library, PubMed, Google Scholar, Embase, Medline, China National Knowledge Infrastructure, China Scientific Journal Database, Chinese Biomedical Literature Database and Wanfang Database from their inception to December 2020. Two researchers will perform data extraction and risk of bias assessment independently. The clinical outcomes including tumor response, overall survival, event-free survival (EFS), quality of life (QoL) and adverse events, were systematically evaluated by using Review Manager 5.3 and Stata 14.0 statistical software.
The results of this study will provide high-quality evidence for the effect of autologous or allogeneic HSC transplantation combined with high-dose chemotherapy on tumor response, survival, and QoL in patients with refractory neuroblastoma.
The conclusions of this meta-analysis will be published in a peer-reviewed journal, and provide more evidence-based guidance in clinical practice.
神经母细胞瘤是儿童常见的实体恶性肿瘤。尽管新的治疗方案不断发展,但高危神经母细胞瘤患者的预后仍然较差。大剂量化疗和造血干细胞(HSC)移植可能改善难治性神经母细胞瘤患者的生存。本研究通过荟萃分析,旨在总结大剂量化疗联合自体或异体 HSC 移植治疗难治性神经母细胞瘤的疗效。
将在 Web of Science、Cochrane Library、PubMed、Google Scholar、Embase、Medline、中国知网、中国科学引文数据库、中国生物医学文献数据库和万方数据库中搜索关于自体或异体 HSC 移植治疗难治性神经母细胞瘤患者的相关临床试验,检索时间从建库至 2020 年 12 月。两位研究者将独立进行数据提取和偏倚风险评估。采用 Review Manager 5.3 和 Stata 14.0 统计软件系统评价肿瘤反应、总生存、无事件生存(EFS)、生活质量(QoL)和不良事件等临床结局。
本研究的结果将为自体或异体 HSC 移植联合大剂量化疗对难治性神经母细胞瘤患者肿瘤反应、生存和 QoL 的影响提供高质量证据。
该荟萃分析的结论将发表在同行评议的期刊上,为临床实践提供更具循证医学指导。