Center for Integrative Medicine, Faculty of Medicine, University of Witten/Herdecke, Herdecke, Germany.
BMC Cancer. 2009 Dec 18;9:451. doi: 10.1186/1471-2407-9-451.
In Europe, extracts from Viscum album (VA-E), the European white-berry mistletoe, are widely used to treat patients with cancer.
We searched several databases such as Cochrane, EMBASE, NCCAM, NLM, DIMDI, CAMbase, and Medline. Inclusion criteria were controlled clinical studies on parameters associated with survival in cancer patients treated with Iscador. Outcome data were extracted as they were given in the publication, and expressed as hazard ratios (HR), their logarithm, and the respective standard errors using standard formulas.
We found 49 publications on the clinical effects of Iscador usage on survival of cancer patients which met our criteria. Among them, 41 studies and strata provided enough data to extract hazard ratios (HR) and their standard errors (Iscador versus no extra treatment). The majority of studies reported positive effects in favour of the Iscador application. Heterogeneity of study results was moderate (I2 = 38.3%, p < 0.0001). The funnel plots were considerably skewed, indicating a publication bias, a notion which is corroborated by statistical means (AC = -1.3, CI: -1.9 to -0.6, p <= 0.0001). A random effect meta-analysis estimated the overall hazard ratio at HR = 0.59 (CI: 0.53 to 0.66, p < 0.0001). Randomized studies showed less effects than non-randomized studies (ratio of HRs: 1.24, CI: 0.79 to 1.92, p = 0.35), and matched-pair studies gave significantly better results than others (ratio of HRs: 0.33; CI: 0.17 to 0.65, p = 0.0012).
Pooled analysis of clinical studies suggests that adjuvant treatment of cancer patients with the mistletoe extract Iscador is associated with a better survival. Despite obvious limitations, and strong hints for a publication bias which limits the evidence found in this meta-analysis, one can not ignore the fact that studies with positive effects of VA-E on survival of cancer patients are accumulating. Future studies evaluating the effects of Iscador should focus on a transparent design and description of endpoints in order to provide greater insight into a treatment often being depreciated as ineffective, but highly valued by cancer patients.
在欧洲,槲寄生(VA-E)的提取物,即欧洲白浆果槲寄生,被广泛用于治疗癌症患者。
我们在 Cochrane、EMBASE、NCCAM、NLM、DIMDI、CAMbase 和 Medline 等数据库中进行了检索。纳入标准为使用 Iscador 治疗癌症患者时与生存相关参数的对照临床试验。提取出版物中给出的结果数据,并使用标准公式将其表示为危害比(HR)、对数及其相应的标准误差。
我们发现了 49 篇关于 Iscador 使用对癌症患者生存影响的临床效果的出版物,这些出版物符合我们的标准。其中,41 项研究和分层提供了足够的数据来提取危害比(HR)及其标准误差(Iscador 与无额外治疗)。大多数研究报告了有利于 Iscador 应用的积极效果。研究结果的异质性为中度(I2=38.3%,p<0.0001)。漏斗图明显偏斜,表明存在发表偏倚,这一观点得到了统计学方法的证实(AC=-1.3,CI:-1.9 至-0.6,p≤0.0001)。随机效应荟萃分析估计总体危害比为 HR=0.59(CI:0.53 至 0.66,p<0.0001)。随机研究显示的效果小于非随机研究(HR 比:1.24,CI:0.79 至 1.92,p=0.35),配对研究的结果明显优于其他研究(HR 比:0.33;CI:0.17 至 0.65,p=0.0012)。
对临床研究的汇总分析表明,用槲寄生提取物 Iscador 辅助治疗癌症患者与生存改善相关。尽管存在明显的局限性,并且强烈提示发表偏倚限制了本荟萃分析中的证据,但人们不能忽视这样一个事实,即关于 VA-E 对癌症患者生存影响的积极研究正在不断积累。未来评估 Iscador 效果的研究应侧重于设计和描述终点的透明度,以便更深入地了解这种治疗方法,因为这种治疗方法经常被贬低为无效,但却受到癌症患者的高度重视。