Horneber M A, Bueschel G, Huber R, Linde K, Rostock M
Medizinische Klinik 5, Arbeitsgruppe Biologische Krebstherapie, Prof.-Ernst-Nathan-Str. 1, Nuernberg, Germany, D-90419.
Cochrane Database Syst Rev. 2008 Apr 16;2008(2):CD003297. doi: 10.1002/14651858.CD003297.pub2.
Mistletoe extracts are commonly used in cancer patients. It is claimed that they improve survival and quality of life (QOL) in cancer patients.
To determine the effectiveness, tolerability and safety of mistletoe extracts given either as monotherapy or adjunct therapy for patients with cancer.
Search sources included the Cochrane Central Register of Controlled Trials (CENTRAL, Issue 3, 2007) Cochrane Complementary Medicine Field Registry of randomized clinical trials (RCTs) and controlled clinical trials, MEDLINE, EMBASE, HEALTHSTAR, INT. HEALTH TECHNOLOGY ASSESSMENT, SOMED, AMED, BIOETHICSLINE, BIOSIS, CancerLit, CATLINE, CISCOM (August 2007). For the search the Standard Operating Procedures of the Information System in Health Economics at the German Institute for Medical Documentation and Information (DIMDI) were utilized. Reference lists of relevant articles and authors extensive files were searched for additional studies. Manufacturers of mistletoe preparations were contacted.
We included RCTs of adults with cancer of any type. The interventions were mistletoe extracts as sole treatments or given concomitantly with chemo- or radiotherapy. The outcome measures were survival times, tumor response, QOL, psychological distress, adverse effects from antineoplastic treatment and safety of mistletoe extracts.
Three review authors independently assessed trials for inclusion in the review. All review authors independently took part in the extraction of data and assessment of study quality and clinical relevance. Disagreements were resolved by consensus. Study authors were contacted where information was unclear. Methodological quality was narratively described and additionally assessed with the Delphi list and the Jadad score. High methodological quality was defined if six out of nine Delphi criteria, or four out of five Jadad criteria were fulfilled. Results were presented qualitatively.
Eighty studies were identified. Fifty-eight were excluded for various reasons, usually as there was no prospective trial design with randomised treatment allocation. Of the 21 included studies 13 provided data on survival, 7 on tumour response, 16 on measures of QOL or psychological outcomes, or prevalence of chemotherapy-related adverse effects and 12 on side effects of mistletoe treatment; overall comprising 3484 randomised cancer patients. Interventions evaluated were 5 preparations of mistletoe extracts from 5 manufacturers and one commercially not available preparation. The general reporting of RCTs was poor. Of the 13 trials investigating survival, 6 showed some evidence of a benefit, but none of them was of high methodological quality. The results of two trials in patients with melanoma and head and neck cancer gave some evidence that the used mistletoe extracts are not effective for improving survival. Of the 16 trials investigating the efficacy of mistletoe extracts for either improving QOL, psychological measures, performance index, symptom scales or the reduction of adverse effects of chemotherapy, 14 showed some evidence of a benefit, but only 2 of them including breast cancer patients during chemotherapy were of higher methodological quality. Data on side effects indicated that, depending on the dose, mistletoe extracts were usually well tolerated and had few side effects.
AUTHORS' CONCLUSIONS: The evidence from RCTs to support the view that the application of mistletoe extracts has impact on survival or leads to an improved ability to fight cancer or to withstand anticancer treatments is weak. Nevertheless, there is some evidence that mistletoe extracts may offer benefits on measures of QOL during chemotherapy for breast cancer, but these results need replication. Overall, more high quality, independent clinical research is needed to truly assess the safety and effectiveness of mistletoe extracts. Patients receiving mistletoe therapy should be encouraged to take part in future trails.
槲寄生提取物常用于癌症患者。据称,它们可提高癌症患者的生存率和生活质量(QOL)。
确定槲寄生提取物作为单一疗法或辅助疗法用于癌症患者的有效性、耐受性和安全性。
检索来源包括Cochrane对照试验中央注册库(CENTRAL,2007年第3期)、Cochrane补充医学领域随机临床试验(RCT)和对照临床试验注册库、MEDLINE、EMBASE、HEALTHSTAR、INT. HEALTH TECHNOLOGY ASSESSMENT、SOMED、AMED、BIOETHICSLINE、BIOSIS、CancerLit、CATLINE、CISCOM(2007年8月)。检索时采用了德国医学文献与信息研究所(DIMDI)卫生经济学信息系统的标准操作程序。检索了相关文章的参考文献列表和作者的大量文件以查找其他研究。还联系了槲寄生制剂的制造商。
我们纳入了任何类型癌症成年患者的RCT。干预措施为槲寄生提取物作为单一治疗或与化疗或放疗同时使用。结局指标为生存时间、肿瘤反应、生活质量、心理困扰、抗肿瘤治疗的不良反应以及槲寄生提取物的安全性。
三位综述作者独立评估试验是否纳入综述。所有综述作者独立参与数据提取以及研究质量和临床相关性评估。分歧通过共识解决。信息不明确时联系研究作者。对方法学质量进行了叙述性描述,并额外使用德尔菲清单和雅达评分进行评估。如果满足九项德尔菲标准中的六项或五项雅达标准中的四项,则定义为方法学质量高。结果进行定性呈现。
共识别出80项研究。58项因各种原因被排除,通常是因为没有随机治疗分配的前瞻性试验设计。在纳入的21项研究中,13项提供了生存数据,7项提供了肿瘤反应数据,16项提供了生活质量或心理结局测量、化疗相关不良反应发生率的数据,12项提供了槲寄生治疗副作用的数据;总共涉及3484例随机分组的癌症患者。评估的干预措施为来自5家制造商的5种槲寄生提取物制剂和一种无商业供应的制剂。RCT的总体报告质量较差。在13项调查生存情况的试验中,6项显示出一些获益证据,但均未达到高方法学质量。两项针对黑色素瘤和头颈癌患者的试验结果提供了一些证据,表明所使用的槲寄生提取物对提高生存率无效。在16项调查槲寄生提取物改善生活质量、心理测量、性能指标、症状量表或减少化疗不良反应疗效的试验中,14项显示出一些获益证据,但其中只有2项包括化疗期间的乳腺癌患者,方法学质量较高。副作用数据表明,根据剂量不同,槲寄生提取物通常耐受性良好且副作用较少。
RCT的证据支持槲寄生提取物的应用对生存有影响或能提高抗癌能力或耐受抗癌治疗能力的观点较为薄弱。然而,有一些证据表明槲寄生提取物可能对乳腺癌化疗期间的生活质量指标有益,但这些结果需要重复验证。总体而言,需要更多高质量、独立的临床研究来真正评估槲寄生提取物的安全性和有效性。应鼓励接受槲寄生治疗的患者参与未来试验。