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Efficacy and safety of mistletoe preparations (Viscum album) for patients with cancer diseases. A systematic review

机译:槲寄生制剂(Viscum album)对癌症患者的功效和安全性。系统评价

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摘要

BACKGROUND: Mistletoe is often used as a complementary approach in oncology. Despite experimental anti-tumour effects and several reviews there remains controversy about its clinical role. PATIENTS AND METHODS: Potentially relevant trials were identified to perform a systematic review (databases: e.g. EMBASE, MEDLINE; hand search: e.g. bibliographies; search terms: e.g. mistletoe). To be included, randomised or comparative clinical trials at least had to examine mistletoe preparations standardized according to manufacturing process and to describe interventions explicitly. Additionally, cohort studies were included for reasons of external validity. Results were summarised in tables. RESULTS: 18 clinical trials (>6,800 participants) were included. Their internal quality was mostly low. Due to heterogeneity between trials a meta-analysis was impossible. Regarding efficacy, findings were inconsistent regarding life expectancy, relation to tumour entity, dosing and treatment duration. Yet, studies indicate that quality of life (QoL) is improved. As these findings do not seem to be limited to one of the different parenteral mistletoe preparations reviewed the treatment may be summarised under the umbrella term 'mistletoe therapy'. Regarding safety, 1 serious adverse event (AE) related to mistletoe was described; non-serious AEs were local reactions at injection site. Allergic reactions were rare. CONCLUSION: Supportive 'mistletoe therapy' seems safe and beneficial for QoL in adult patients with solid tumours. But there is an urgent need to confirm its efficacy in patient-centred care in a complex oncological setting. This has to be evaluated systematically in prospective observational trials with validated, multidimensional patient-rated QoL questionnaires and comparisons of different preparations and dosages. Copyright 2009 S. Karger AG, Basel.
机译:背景:槲寄生经常被用作肿瘤学的补充方法。尽管有实验性的抗肿瘤作用,并且有一些评论,但关于其临床作用仍存在争议。患者和方法:确定了可能相关的试验以进行系统评价(数据库:例如EMBASE,MEDLINE;手动搜索:例如书目;搜索词:例如槲寄生)。包括在内的随机或比较临床试验至少必须检查根据制造工艺标准化的槲寄生制剂,并明确描述干预措施。另外,出于外部有效性的原因,纳入了队列研究。结果总结在表中。结果:包括18个临床试验(> 6,800名参与者)。他们的内部素质大多较低。由于试验之间的异质性,因此无法进行荟萃分析。关于功效,关于预期寿命,与肿瘤实体,剂量和治疗时间的关系不一致。然而,研究表明生活质量(QoL)得到改善。由于这些发现似乎不限于所审查的不同肠胃外槲寄生制剂之一,因此可将其概括为“槲寄生疗法”一词。关于安全性,描述了1个与槲寄生有关的严重不良事件(AE);非严重不良事件是注射部位的局部反应。过敏反应很少见。结论:支持性的“槲寄生疗法”对于成年实体瘤患者的QoL似乎是安全且有益的。但是,迫切需要确认其在复杂的肿瘤环境中在以患者为中心的护理中的功效。必须在前瞻性观察性试验中使用经过验证的,多维患者评分的QoL调查表以及不同制剂和剂量的比较,系统地对此进行评估。版权所有2009 S. Karger AG,巴塞尔。

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