Gardiner Breeana, Wardill Hannah R, O'Connor Graeme, Hargrave Darren, Lett Aaron M
Department of Nutrition and Dietetics, Great Ormond Street Hospital for Children, Great Ormond Street, London, WC1N 3JH, UK; Section of Nutrition, Department of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London, W12 0NN, UK.
School of Biomedicine, The University of Adelaide, Adelaide, South Australia, 5005, Australia; Supportive Oncology Research Group, Precision Cancer Medicine, South Australian Health and Medical Research Institute, Adelaide, South Australia, 5000, Australia.
Clin Nutr. 2025 Jan;44:86-100. doi: 10.1016/j.clnu.2024.11.022. Epub 2024 Nov 19.
BACKGROUND & AIMS: Cancer therapy is associated with a range of toxicities that severely impact patient well-being and a range of clinical outcomes. Dietary fibre/prebiotics characteristically improve the gastrointestinal microenvironment, which consequently elicits beneficial downstream effects that could be relevant to the prevention and management of treatment-related toxicities. Despite the compelling theoretical scientific rationale there has been limited effort to synthesise the available evidence to conclude such scientific underpinning to the clinical use of fibre/prebiotics in cancer patients. Therefore, this systematic review aimed to evaluate the clinical impact of fibre/prebiotic-based interventions on gastrointestinal-side effects; gastrointestinal-microbiome; clinical outcomes; nutrition status and body composition; and quality-of-life in children and adults being treated for cancer or undergoing a haematopoietic stem cell transplant (HSCT).
This study was conducted in adherence to PRISMA guidelines, and the protocol was published prospectively with PROSPERO (CRD42022299428). Three databases (MEDLINE (Ovid), CINHAL, EMBASE) were searched from inception to December 2023. All articles were assessed for bias using the Cochrane risk-of-bias tool RoB 2.0 (for RCTs) and ROBINS-I (for non-RCTs).
A total of 9989 de-duplicated records were identified, of these, 14 (paediatrics [n = 1], adults [n = 13]) met the inclusion criteria (randomised controlled trials (RCT) [n = 11], observational or non-RCTs [n = 3]). The risk-of-bias was graded to be serious/high (n = 6); moderate/some concerns (n = 7); low (n = 1). Interventions included prebiotic supplement (n = 8), nutrition supplement/formula with added fibre/prebiotic (n = 3) and dietary modification (n = 3). The dose of fibre intervention ranged from 2.4g to 30g per day. Substantial heterogeneity of target parameters was identified across a range all outcome categories, precluding definitive conclusions.
The scientific rationale for fibre/prebiotics-based interventions for the prevention or management of cancer treatment-related toxicities is compelling. However, it is clear that the scientific and clinical field remains disconnected in how to effectively translate this approach to improve cancer outcomes. High-quality intervention studies translatable to clinical practice are now evidently crucial to determine if and how fibre/prebiotics should be used to support people undergoing cancer or HSCT therapy.
癌症治疗会引发一系列毒性反应,严重影响患者的健康状况及一系列临床结局。膳食纤维/益生元通常可改善胃肠道微环境,进而产生有益的下游效应,这可能与预防和管理治疗相关毒性有关。尽管有令人信服的理论科学依据,但在综合现有证据以确定膳食纤维/益生元在癌症患者临床应用中的科学基础方面,所做的努力有限。因此,本系统评价旨在评估基于膳食纤维/益生元的干预措施对接受癌症治疗或造血干细胞移植(HSCT)的儿童和成人的胃肠道副作用、胃肠道微生物群、临床结局、营养状况和身体成分以及生活质量的临床影响。
本研究严格遵循PRISMA指南进行,研究方案已在PROSPERO(CRD42022299428)上前瞻性发表。检索了三个数据库(MEDLINE(Ovid)、CINHAL、EMBASE),检索时间从建库至2023年12月。使用Cochrane偏倚风险工具RoB 2.0(用于随机对照试验)和ROBINS - I(用于非随机对照试验)对所有文章进行偏倚评估。
共识别出9989条去重记录,其中14篇(儿科[n = 1],成人[n = 13])符合纳入标准(随机对照试验(RCT)[n = 11],观察性研究或非随机对照试验[n = 3])。偏倚风险被评为严重/高(n = 6);中度/有些担忧(n = 7);低(n = 1)。干预措施包括益生元补充剂(n = 8)、添加了膳食纤维/益生元的营养补充剂/配方奶粉(n = 3)和饮食调整(n = 3)。膳食纤维干预的剂量范围为每天2.4克至30克。在所有结局类别中均发现目标参数存在很大异质性,无法得出明确结论。
基于膳食纤维/益生元的干预措施用于预防或管理癌症治疗相关毒性的科学依据很有说服力。然而,很明显,在如何有效地将这种方法转化以改善癌症结局方面,科学和临床领域仍然脱节。现在,高质量的可转化为临床实践的干预研究对于确定是否以及如何使用膳食纤维/益生元来支持接受癌症或HSCT治疗的患者显然至关重要。