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1.
J Pharm Pharmacol ; 70(2): 159-177, 2018 Feb.
Article in English | MEDLINE | ID: mdl-29034952

ABSTRACT

OBJECTIVES: The aim of this study was to review and highlight traditional and ethnobotanical uses, phytochemical constituents, IP status, biological activity and pharmacological activity of Viscum articulatum. METHODS: Thorough literature searches were performed on Viscum articulatum, and data were analysed for reported traditional uses, pharmacological activity, phytochemicals present and patents filed. Scientific and patent databases such as PubMed, Science Direct, Google Scholar, Google patents, USPTO and Espacenet were searched using different keywords. KEY FINDINGS: Viscum articulatum has been traditionally used in different parts of the world for treatment of various ailments. Almost all the parts such as leaves, root, stem and bark are having medicinal values and are reported for their uses in Ayurvedic and Chinese system of medicine for the management of various diseases. Modern scientific studies demonstrate efficacy of this plant against hypertension, ulcer, epilepsy, inflammation, wound, nephrotoxicity, HIV, cancer, etc. Major bioactive phytochemicals include oleanolic acid, betulinic acid, eriodictyol, naringenin, ß-amyrin acetate, visartisides, etc. CONCLUSIONS: Side effects of allopathic medicines have created a global opportunity, acceptance and demand for phytomedicines. Viscum articulatum could be an excellent source of effective and safe phytomedicine for various ailments if focused translational efforts are undertaken by integrating the existing outcomes of researches.


Subject(s)
Medicine, Traditional , Phytochemicals/therapeutic use , Plant Extracts/therapeutic use , Viscum/chemistry , Animals , Humans , Phytochemicals/adverse effects , Phytochemicals/isolation & purification , Phytotherapy , Plant Extracts/adverse effects , Plant Extracts/isolation & purification , Plants, Medicinal , Viscum/adverse effects
2.
Arzneimittelforschung ; 55(1): 38-49, 2005.
Article in English | MEDLINE | ID: mdl-15727163

ABSTRACT

BACKGROUND: Mistletoe therapy is the most frequently used complementary treatment in cancer patients in Germany and Switzerland. However, its safety and efficacy were controversially discussed, also in case of malignant melanoma (MM). OBJECTIVES: The present study should evaluate the therapeutic safety and efficacy of a long-term therapy with a standardized fermented European mistletoe (Viscum album L.) extract Iscador (FME) during post-surgical aftercare of primary intermediate to high-risk MM (UICC/AJCC stage II-III) patients and compare it with an untreated parallel control group from the same cohort. METHODS: The study was designed as a multicenter, comparative, retrolective, epidemiological cohort study with parallel groups, carried out according to the guidelines of Good Epidemiological Practice (GEP). All patients suffered from surgically treated and histopathologically confirmed primary MM in UICC/AJCC stage II-III without distant metastases. In the study group, FME was administered subcutaneously 2-3 times weekly for at least three months, while the untreated control group was merely observed ("watchful waiting"). In both groups some patients also received radio-, chemo-, and/or immunotherapy. The patients were followed until the last visit or until death. Unselected, chronologically ordered, and standardized anonymous data from medical records that satisfied the predefined eligibility criteria were included for the "per protocol" analysis. Safety was assessed by the number of patients with FME-associated adverse drug reactions (ADRs) and by the search for tumor enhancement. The primary endpoint of efficacy was the adjusted tumor-related survival. Secondary end-points were the overall-, the disease-free- and the brain metastasis-free survival. The survival results were analyzed after adjustment for baseline imbalances, treatment regimens and other potential confounders by the Cox proportional hazard regression method. RESULTS: 686 eligible patients (329 FME vs. 357 controls) from 35 centers were observed for a median aftercare of 81 vs. 52 months. The median FME therapy duration was 30 months. At baseline, both groups were comparable concerning demography, tumor history and risk factors for progression. Additional adjuvant chemotherapy was more frequent in the study group, while immunotherapy was more frequent in the control group. Eleven patients (3.3 %) developed systemic ADRs attributed to the FME-treatment, and 42 patients (12.8 %) developed local ADRs, with mild to intermediate (WHO/CTC grade 1-2) ADR severity and spontaneous resolution in most cases. In six patients the ADRs resulted in therapy termination. Life-threatening ADRs, ADR-related mortality or tumor enhancement were not observed. On the contrary, the incidence rate of lung metastases and the adjusted hazard ratio for brain metastases were significantly lower in the FME group. In the course of the study and during aftercare a total of 212 (30.9 %) patients relapsed or progressed, and 107 (15.6 %) died. A significantly longer tumor-related survival was found in the FME group when compared with the untreated controls (unadjusted tumor-related mortality rate 8.9 % vs. 10.7 %, Kaplan-Meier estimate, Log-rank test, p = 0.017), which was confirmed after adjusting for potential confounders by the tumor-related mortality hazard ratio estimate HR (95 % confidence intervals) = 0.41 (0.23-0.71), p = 0.002. The adjusted HR results of the overall survival, disease-free survival, and the brain metastases-free survival were also significantly superior in the FME group. CONCLUSION: The long-term FME treatment in patients with primary intermediate to high-risk MM appears safe. Tumor enhancement was not observed. When compared with an untreated parallel control group from the same cohort, the results of the FME treatment suggested a significant survival benefit in primary stage II-III MM patients. These results on survival warrant reconfirmation in a prospective randomized clinical trial with optimized study design and treatment conditions.


Subject(s)
Antineoplastic Agents, Phytogenic/therapeutic use , Melanoma/drug therapy , Phytotherapy , Viscum , Antineoplastic Agents, Phytogenic/adverse effects , Cohort Studies , Endpoint Determination , Female , Fermentation , Humans , Male , Melanoma/pathology , Middle Aged , Phytotherapy/adverse effects , Quality Control , Retrospective Studies , Survival Analysis , Treatment Outcome , Viscum/adverse effects
3.
Allergol Immunopathol (Madr) ; 29(5): 201-3, 2001.
Article in English | MEDLINE | ID: mdl-11720654

ABSTRACT

Mistletoe (Viscum album) is a plant that is semiparasitic of several trees: apple, oak, pine trees, etc. Because of the probable cytolytic action of one of the leaf's most abundant composites, in some countries mistletoe is used as a complementary medicine. Although only a few adverse reactions have been noted (cephalea, fever), cases of anaphylactic shock have been described. We present three cases of severe reaction after injection of mistletoe extract. Two of the patients had cancer. The third, whose brother had cancer, used the plant for preventive purposes. We discuss the danger of possible severe reactions due to the use of products employed in so-called alternative therapies.


Subject(s)
Anaphylaxis/chemically induced , Anticarcinogenic Agents/adverse effects , Antineoplastic Agents, Phytogenic/adverse effects , Drug Hypersensitivity/etiology , Phytotherapy/adverse effects , Plant Preparations , Plant Proteins , Toxins, Biological/adverse effects , Viscum/adverse effects , Adenocarcinoma/drug therapy , Adenocarcinoma/surgery , Adult , Aged , Anticarcinogenic Agents/administration & dosage , Anticarcinogenic Agents/immunology , Antineoplastic Agents, Phytogenic/administration & dosage , Antineoplastic Agents, Phytogenic/immunology , Combined Modality Therapy , Female , Humans , Immunoglobulin E/immunology , Intradermal Tests , Male , Multiple Sclerosis/drug therapy , Neoplasm Recurrence, Local/drug therapy , Plant Extracts/administration & dosage , Plant Extracts/adverse effects , Plant Extracts/immunology , Ribosome Inactivating Proteins, Type 2 , Toxins, Biological/administration & dosage , Toxins, Biological/immunology , Uterine Neoplasms/drug therapy , Uterine Neoplasms/surgery , Viscum/immunology
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