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欧洲槲寄生(白果槲寄生)制剂瘤内应用在肿瘤学中的使用及安全性

Use and safety of intratumoral application of European mistletoe (Viscum album L) preparations in Oncology.

作者信息

Steele Megan L, Axtner Jan, Happe Antje, Kröz Matthias, Matthes Harald, Schad Friedemann

机构信息

Research Institute Havelhoehe, Berlin, Germany.

Research Institute Havelhoehe, Berlin, Germany Witten/Herdecke University, Herdecke, Germany.

出版信息

Integr Cancer Ther. 2015 Mar;14(2):140-8. doi: 10.1177/1534735414563977. Epub 2014 Dec 30.

Abstract

BACKGROUND

Intratumoral (IT) injection of European mistletoe (Viscum album L) preparations might induce local tumor response through combined cytotoxic and immunomodulatory actions of the preparations. Although promising in vitro and in vivo data, along with clinical case studies suggest the need for validation of this hypothesis in prospective trials, the safety of IT mistletoe injections has yet to be thoroughly assessed.

METHODS

The present study summarizes the practice and safety of off-label IT mistletoe therapy within the Network Oncology, a conjoint clinical registry of German hospitals and outpatients specialized in anthroposophic and integrative medicine. Demographic, diagnosis and treatment data of cancer patients who received IT mistletoe applications between 2007 and 2013 were assessed. Suspected adverse drug reactions (ADRs) were analyzed in terms of type, frequency, severity, seriousness and potential risk factors.

RESULTS

A total of 123 cancer patients received 862 IT mistletoe injections (preparations from Abnoba, Helixor and Iscucin). The most commonly applied preparations were Abnoba viscum Fraxini (71 patients) and Helixor Mali (54 patients). Of the total patients, 26 patients (21.1%) experienced 74 ADRs. All ADRs were in response to either Abnoba viscum Fraxini (25.4% of exposed patients) or Helixor Mali (18.5% of exposed patients). ADRs were mostly body temperature or immune related and of mild (83.8%) or moderate (14.9%) intensity. Only one possible ADR was described as severe (hypertension) and no serious ADRs occurred. The frequency of ADRs to IT mistletoe injections was 3 times and 5 times higher than has previously been found for subcutaneous and intravenous applications of mistletoe, respectively.

CONCLUSION

IT injection of mistletoe preparations resulted in a relatively high frequency of ADRs. Nearly all ADRs were mild to moderate however, and no serious ADRs occurred. Furthermore, it is possible that immune-related ADRs such as pyrexia and local inflammatory reactions might be critical for tumor response. In light of these results, IT mistletoe therapy seems to be safe and prospective trials are recommended.

摘要

背景

瘤内(IT)注射欧洲槲寄生(欧洲白槲寄生)制剂可能通过该制剂的细胞毒性和免疫调节联合作用诱导局部肿瘤反应。尽管体外和体内数据很有前景,同时临床病例研究表明需要在前瞻性试验中验证这一假设,但瘤内注射槲寄生的安全性尚未得到全面评估。

方法

本研究总结了德国专门从事人智医学和综合医学的医院及门诊联合临床登记处网络肿瘤学中未按标签说明使用瘤内槲寄生疗法的实践和安全性。评估了2007年至2013年间接受瘤内注射槲寄生的癌症患者的人口统计学、诊断和治疗数据。对疑似药物不良反应(ADR)的类型、频率、严重程度、严重性和潜在风险因素进行了分析。

结果

共有123名癌症患者接受了862次瘤内注射槲寄生(来自Abnoba、Helixor和Iscucin的制剂)。最常用的制剂是Abnoba viscum Fraxini(71例患者)和Helixor Mali(54例患者)。在所有患者中,26例患者(21.1%)出现了74次药物不良反应。所有药物不良反应均针对Abnoba viscum Fraxini(暴露患者的25.4%)或Helixor Mali(暴露患者的18.5%)。药物不良反应大多与体温或免疫相关,强度为轻度(83.8%)或中度(14.9%)。仅有一种可能的药物不良反应被描述为严重(高血压),未发生严重药物不良反应。瘤内注射槲寄生的药物不良反应发生率分别比先前皮下和静脉注射槲寄生的发生率高3倍和5倍。

结论

瘤内注射槲寄生制剂导致相对较高的药物不良反应发生率。然而,几乎所有药物不良反应均为轻度至中度,未发生严重药物不良反应。此外,发热和局部炎症反应等免疫相关药物不良反应可能对肿瘤反应至关重要。鉴于这些结果,瘤内槲寄生疗法似乎是安全的,建议进行前瞻性试验。

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