Flinders Health and Medical Research Institute - Cancer, Flinders University, Adelaide, South Australia, Australia
Flinders Health and Medical Research Institute - Cancer, Flinders University College of Medicine and Public Health, Bedford Park, South Australia, Australia.
BMJ Open. 2022 Jan 3;12(1):e053308. doi: 10.1136/bmjopen-2021-053308.
Childhood leukaemia is the most common type of cancer in children and represents among 25% of the diagnoses in children <15 years old. Childhood survival rates have significantly improved within the last 40 years due to a rapid advancement in therapeutic interventions. However, in high-risk groups, survival rates remain poor. Pharmacokinetic (PK) data of cancer medications in children are limited and thus current dosing regimens are based on studies with small sample sizes. In adults, large variability in PK is observed and dose individualisation (plasma concentration guided dosing) has been associated with improved clinical outcomes; whether this is true for children is still unknown. This provides an opportunity to explore this strategy in children to potentially reduce toxicities and ensure optimal dosing. This paper will provide a protocol to systematically review studies that have used dose individualisation of drugs used in the treatment of childhood leukaemias.
Systematic review methodology will be applied to identify, select and extract data from published plasma guided dosing studies conducted in a paediatric leukaemia cohort. Databases (eg, Ovid Embase, Ovid MEDLINE, Ovid Cochrane) and clinical trial registries (CENTRAL, ClinicalTrials.gov and ISRCTN) will be used to perform the systematic literature search (up until February 2021). Only full empirical studies will be included, with primary clinical outcomes (progression-free survival, toxicities, minimal residual disease status, complete cytogenetic response, partial cytogenetic response and major molecular response) being used to decide whether the study will be included. The quality of included studies will be undertaken, with a subgroup analysis where appropriate.
This systematic review will not require ethics approval as there will not be collection of primary data. Findings of this review will be made available through publications in peer-reviewed journals and conference presentations. Gaps will be identified in current literature to inform future-related research.
CRD42021225045.
儿童白血病是儿童中最常见的癌症类型,占 15 岁以下儿童诊断的 25%。由于治疗干预的快速发展,过去 40 年来,儿童的生存率显著提高。然而,在高危人群中,生存率仍然很差。儿童癌症药物的药代动力学(PK)数据有限,因此目前的剂量方案基于样本量较小的研究。在成人中,观察到 PK 有很大的变异性,剂量个体化(基于血浆浓度的给药)与改善临床结局相关;对于儿童是否如此还不清楚。这为在儿童中探索这种策略提供了机会,以潜在降低毒性并确保最佳剂量。本文将提供一份方案,以系统地回顾使用儿童白血病治疗药物进行剂量个体化的研究。
将应用系统评价方法从发表的儿科白血病队列中进行的血浆引导剂量研究中识别、选择和提取数据。数据库(如 Ovid Embase、Ovid MEDLINE、Ovid Cochrane)和临床试验注册库(CENTRAL、ClinicalTrials.gov 和 ISRCTN)将用于进行系统文献检索(截至 2021 年 2 月)。仅纳入全实证研究,主要临床结局(无进展生存期、毒性、微小残留病状态、完全细胞遗传学缓解、部分细胞遗传学缓解和主要分子缓解)用于决定是否纳入研究。将对纳入研究的质量进行评估,并在适当的情况下进行亚组分析。
由于不会收集原始数据,因此本次系统评价不需要伦理批准。该综述的结果将通过在同行评议期刊上发表和会议报告的形式提供。将确定当前文献中的差距,以为未来的相关研究提供信息。
PROSPERO 注册号:CRD42021225045。