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癌症患者皮下用槲寄生提取物(Viscum album L.)治疗的不良反应和预期效果。

Adverse Drug Reactions and Expected Effects to Therapy with Subcutaneous Mistletoe Extracts (Viscum album L.) in Cancer Patients.

机构信息

Research Institute Havelhoehe, 14089 Berlin, Germany.

Research Institute Havelhoehe, 14089 Berlin, Germany ; Hospital Havelhoehe, 14089 Berlin, Germany ; Institute for Social Medicine, Epidemiology and Health Economics, Charité-University Medical Center, 10117 Berlin, Germany.

出版信息

Evid Based Complement Alternat Med. 2014;2014:724258. doi: 10.1155/2014/724258. Epub 2014 Jan 19.

Abstract

Background. In Europe, mistletoe extracts are widely used as a complementary cancer therapy. We assessed the safety of subcutaneous mistletoe as a conjunctive therapy in cancer patients within an anthroposophic medicine setting in Germany. Methods. A multicentre, observational study was performed within the Network Oncology. Suspected mistletoe adverse drug reactions (ADRs) were described by frequency, causality, severity, and seriousness. Potential risk factors, dose relationships and drug-drug interactions were investigated. Results. Of 1923 cancer patients treated with subcutaneous mistletoe extracts, 283 patients (14.7%) reported 427 expected effects (local reactions <5 cm and increased body temperature <38°C). ADRs were documented in 162 (8.4%) patients who reported a total of 264 events. ADRs were mild (50.8%), moderate (45.1%), or severe (4.2%). All were nonserious. Logistic regression analysis revealed that expected effects were more common in females, while immunoreactivity decreased with increasing age and tumour stage. No risk factors were identified for ADRs. ADR frequency increased as mistletoe dose increased, while fewer ADRs occurred during mistletoe therapy received concurrent with conventional therapies. Conclusion. The results of this study indicate that mistletoe therapy is safe. ADRs were mostly mild to moderate in intensity and appear to be dose-related and explained by the immune-stimulating, pharmacological activity of mistletoe.

摘要

背景

在欧洲,槲寄生提取物被广泛用作癌症的辅助治疗方法。我们评估了在德国顺势疗法环境下,将皮下使用槲寄生作为联合疗法用于癌症患者的安全性。

方法

在网络肿瘤学中进行了一项多中心、观察性研究。通过频率、因果关系、严重程度和严重性来描述疑似槲寄生药物不良反应(ADR)。调查了潜在的危险因素、剂量关系和药物相互作用。

结果

在接受皮下使用槲寄生提取物治疗的 1923 名癌症患者中,283 名(14.7%)患者报告了 427 种预期的效果(局部反应<5cm 和体温升高<38°C)。162 名(8.4%)患者记录了 264 项 ADR 事件。ADR 为轻度(50.8%)、中度(45.1%)或重度(4.2%)。所有 ADR 均为非严重。逻辑回归分析显示,预期效果在女性中更为常见,而免疫反应随着年龄和肿瘤分期的增加而降低。未发现 ADR 的危险因素。随着槲寄生剂量的增加,ADR 的频率增加,而在同时接受常规治疗的槲寄生治疗期间,ADR 发生的次数较少。

结论

这项研究的结果表明,槲寄生治疗是安全的。ADR 大多为轻度至中度,似乎与剂量有关,并可通过槲寄生的免疫刺激、药理学活性来解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/224b/3929984/44a9ceb87e30/ECAM2014-724258.001.jpg

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