Table 2. Use of Other Mistletoe Products in Cancer Treatment: Clinical Reports Describing Therapeutic Endpointsa
| Reference Citation(s) | Type of Study | Product Tested | Type(s) of Cancer | No. of Patients: Enrolled; Treated; Controlb | Strongest Benefit Reportedc | Concurrent Therapyd | Level of Evidence Scoree |
| [3] | Randomized trial | Eurixor | Bladder, noninvasive | 45; 23; 22 | None | No | 1iiDi |
| [1,33] | Randomized trial | Eurixor | Brain, glioma; 74% of patients, stages III–IV; 26% of patients, no stage information | 47; 20; 18 | Improved survival, stages III–IV patients only | Yes | 1iiA |
| [45,46] | Randomized trial | Eurixor | Colorectal, metastatic | 107; 38; 41 | Improved quality of life | Yes | 1iiA |
| [2] | Randomized trial | Eurixor | Head and neck, squamous cell, stages I–IV | 495; 235f; 242f | None | Yesf | 1iiA |
| [37] | Randomized trial | Helixor | Breast, stages I–III | 692; 192; 274 | Improved survival | Yes | 1iiA |
| [38] | Randomized trial | Helixor | Colorectal, metastatic | 60; 20; 20 | Improved mean survival | Yes | 1iiA |
| [13] | Randomized controlled trial | PS76A (Lektin) | Breast | 352; 176; 176 | Improved quality of life | Yes | 1iC |
| [35] | Randomized trial | Isorel | Colorectal | 64; 50; 14 | Improved survival and tolerance to either adjuvant or palliative treatment | Yes | 1iiA |
| [36] | Nonrandomized controlled trial | Isorel | Digestive tract | 70; 40; 30 | Enhanced cellular immunity and improved quality of life | No | 2C |
| [43] | Nonrandomized controlled trial | abnobaVISCUM Quercus | Metastatic colorectal | 25; 25; none | None | Yes | 2Diii |
| [23] | Nonrandomized controlled trial | Viscum fraxini-2 | Hepatocellular carcinoma | 23; 23; none | Improved survival | No | 2Dii |
| No. = number. | ||||||
| aRefer to text and the NCI Dictionary of Cancer Terms for additional information and definition of terms. | ||||||
| bNumber of patients treated plus number of patients controlled may not equal number of patients enrolled; number of patients enrolled = number of patients initially recruited/considered by the researchers who conducted a study; number of patients treated = number of enrolled patients who were administered the treatment being studied AND for whom results were reported; historical control subjects are not included in number of patients enrolled. | ||||||
| cStrongest evidence reported that the treatment under study has anticancer activity or otherwise improves the well-being of cancer patients. | ||||||
| dChemotherapy, radiation therapy, hormonal therapy, or cytokine therapy administered/allowed at the same time as mistletoe therapy. | ||||||
| eFor information about levels of evidence analysis and an explanation of the level of evidence scores, refer to Levels of Evidence for Human Studies of Cancer Complementary and Alternative Medicine. | ||||||
| fThis trial was a four-arm trial; patients were randomly assigned to surgery only or to surgery plus radiation therapy, followed by a second randomization to no mistletoe treatment or to treatment with Eurixor; the resulting treatment groups contained the following numbers of evaluable patients: surgery only = 105, surgery plus Eurixor = 97, surgery plus radiation therapy = 137, and surgery plus radiation therapy plus Eurixor = 138; radiation therapy and Eurixor treatment overlapped; no treatment approach was superior in terms of disease-free survival, disease-specific survival, improvement in quality of life, or stimulation of the immune system; in the table, mistletoe-treated and nontreated (control) patients were grouped (i.e., number treated = 97 + 138 = 235, and number control = 105 + 137 = 242). |
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