Iscador/Mistletoe
http://www.cancure.org/iscador_mistletoe.htm
Mistletoe, or Viscum album is a
semi-parasitic plant that grows on oaks and other trees in Europe and Asia.
Mistletoe is also found in America and Korea, but normally only the European
species is used in the treatment of cancer, inflammatory conditions and AIDS.
The leaves, twigs, and berries are what is used to make these herbal medicines.
Because the medicinal doses are small (it can be poisonous in large doses),
many believe it to be "homeopathic," but it isn't.
Mistletoe was first proposed for the
treatment of cancer in 1920 by Rudolph Steiner, an Austrian Swiss physician who
founded the Society for Cancer Research to promote mistletoe extracts and
anthroposophical medicine.
Mistletoe extracts are marketed under several
trade names, such as Iscador, Helixor, Eurixor, and Isorel, most of which are
available in Europe. Weleda AG manufactures Iscador., which consists of
fermented extracts of mistletoe, sometimes combined with trace amounts of silver,
copper or mercury. In the United States, any of these extracts must be
prescribed by a physician. However, most doctors in the US do not use it.
Though mistletoe is not commonly used in the United States, it is allowed by
compassionate use. Physicians in the United States can order Iscador directly
from European manufacturers. Oral/liquid mistletoe can be ordered by your
physician by contacting Weleda AG through www.usa.weleda.com or by calling
800-241-1030.
Some of the alternative physicians that use it include: San Diego Clinic and Stella Maris in Mexico, Dr. Jesse Stoff in Arizona, Atkins Center in NY, Lukas Clinic in Switzerland, Joseph Brenner, M.D. in Tel-Aviv, Klinik St George and Hufeland Clinic in Germany, and Humlegaarden in Denmark. If you are aware of any clinical trials using mistletoe or any other clinics using it, please email our webmaster to add this information to our website.
For a list of clinical trials using mistletoe, go to: http://www.foreigntrials.com/trials_list.html.
Mistletoe preparations are used to stimulate
the immune system, to kill cancer cells, and to help reduce tumor size. It may
also help improve the quality of life and survival of some cancer patients,
especially those using chemo and radiation, and may help reduce pain and side
effects of these treatments. In addition, a German study done by Dr. Ronald
Grossarth-Maticek of the Institute for Preventive Medicine in Heidelberg shows
that, when used as adjunctive treatment in patients with a variety of cancers,
it can increase survival time by as much as 40%.
Typical Treatment:
Typical Treatment:
A typical treatment course can last several
months to years. The doses are gradually increased and adjusted depending on
the patient's general condition, sex, age, and type of cancer. Mistletoe is
typically given by subcutaneous injection, but it sometimes is injected
directly into the tumor particularly on the liver, esophagus and cervix. It may
also be taken orally in tumors of the brain and spinal cord.
What studies show:
In animal studies, mistletoe preparations
have helped fight some forms of cancer. The best results with Iscador are
claimed for its use with solid tumors both before and after surgery and
radiation. Given 10 to 14 days before surgery, it is thought to help prevent
metastatic spread due to surgery and to promote recovery and it is also used
for advanced stage, inoperable solid tumors, especially cancers of the bladder,
stomach, intestine, genital organs, and skin. It is also claimed that bone
metastases are retarded in some cases. Results appear less promising for
inoperable cancers of the breast, lungs and esophagus. It is thought that tumor
growth slows or stops, and then gradual regression begins. It is believed that
tumor cells are transformed first to a semi-malignant form, then to chronic
inflammation and finally to normal tissue.
Mistletoe contains a cytotoxic lectin, viscumin. It also contains a number of cytotoxic proteins and polypetides (viscotoxins). Various lectins are both cytotoxic and immunostimulatory. It induces tumor necrosis, increases natural killer cell activity, increases production of interleukins 1 and 6; activates macrophages; induces programmed cell death (apoptosis), and protects DNA in normal cells during chemotherapy.
Mistletoe contains a cytotoxic lectin, viscumin. It also contains a number of cytotoxic proteins and polypetides (viscotoxins). Various lectins are both cytotoxic and immunostimulatory. It induces tumor necrosis, increases natural killer cell activity, increases production of interleukins 1 and 6; activates macrophages; induces programmed cell death (apoptosis), and protects DNA in normal cells during chemotherapy.
Side effects and possible risks:
Commercial mistletoe extracts generally have
minimal side effects, but in rare cases allergic symptoms including
anaphylactic reactions have been reported. It usually produces an increase in
body temperature and flu-like symptoms. In addition, the injection site can
become inflamed and abdominal pain with nausea may occur. Other side effects
include: upset stomach, vomiting, diarrhea, chills, fever, headaches, chest
pain, and low blood pressure. Overdoses, however, can cause severe poisoning
including seizures, coma and death. Even a few leaves or berries can cause
poisoning, so never eat part of a mistletoe plant and keep the plants away from
animals and children. In addition, because the preparation contains tyramine,
patients on any type of monoamine oxidase (MAO) inhibitor antidepressant should
not take it. The combination can cause dangerously high blood pressure. People
with heart problems should also be careful, since it raises blood pressure and
accelerates the pulse. Therapy is normally discontinued in case of high
temperature over 38ÂșC. Some research indicates Iscador injections should not be
administered during the first days of the menstrual period. Seizures and death
have been reported. This product should only be used in a closely supervised
setting, and should not be used for normal consumption - reasons mistletoe
products must be prescribed by a physician.
To avoid potential interactions, be sure to let your health care provider know if you use this or any other type of complementary therapy, and always take under the advice and supervision of a health practioner.
For research or books on iscador/mistletoe, go to Lukas Clinic website at http://www.lukasklinik.ch/English/Default1.htm. They use these products in their treatment programs. Or, go to www.sph.uth.tmc.edu/utcam/summary/mistletoe.htm or http://commonweal.org/herbs.html.
If you have used this product, please contact our webmaster with information on your experience.
Most Cancer Patients Use Complementary Therapies
LONDON (Reuters) July 15, 2002 - More than half of
all cancer patients are using complementary therapies to cope with the side
effects of hospital-based therapies, according to a report published Sunday.
Market consultant Datamonitor said as many as 60% of cancer patients in certain
European countries, and 80% in the United States, used special diets, vitamin
supplements, herbal remedies or acupuncture. It said European use of
complementary and alternative medicines appeared highest in Germany where
products such as mistletoe had become established folk remedies. Datamonitor
estimated the global market for complementary and alternative medicines used by
cancer patients could be as high as $18 billion annually, rivaling the sales of
many traditional pharmaceutical approaches.
The report warned that information published on Web sites about herbal remedies was not always accurate and advised patients to consult a physician before using them. "Some herbal products or diets can affect how prescription cancer drugs are absorbed, or can increase certain side effects of mainstream cancer therapies," according to the report.
"Patients taking complementary medicines need to share their use of these products with their oncologist, for the patients' safety and for the patients' best chance of fighting cancer," it added.
The report forecast that increased scientific studies of alternative medicines could lead to the discovery of new drugs. Complementary medicine and pharmaceutical drug development could move closer to each other, perhaps resulting in novel therapies, new manufacturing companies and commercially successful partnerships.
Enzyme may Help Curb Disease
Jul. 19, 2002 (Ivanhoe Newswire) -- New research
shows an enzyme that corrects mutations in genes could be a key factor in
reducing a person's susceptibility to diseases such as hemophilia, cancer and
cystic fibrosis. Researchers from Cardiff University in Wales and the
University of Edinburgh in Scotland have found the MBD4 enzyme could protect
people from gene mutations that can lead to diseases.
Different combinations of genes are expressed in
different cells. For example, a different combination of genes is expressed in
heart cells as compared to liver cells. Researchers say mutations in these
genes can lead to serious diseases, such as cancer. They say, although factors
such as cigarette smoke and dietary habits may trigger genetic mutations, a lot
of gene damage is caused simply by the natural chemistry that goes on in the
human body. When a mutation occurs, the genes stop doing their "jobs"
effectively.
Researchers say one in three genetic changes or
mutations that causes disease in people can be attributed to methyl-groups.
Methyl-groups work to shut down genes, but in doing so significantly increase
the risk of genetic mutation. Researchers have found the MBD4 enzyme attempts
to repair the damage caused by methyl-groups before they cause harm.
Alan Clarke, a researcher from Cardiff University,
says, "It is very likely the MBD4 is a key defense against self-inflicted
gene damage in humans." In this study of lab animals, Professor Clarke and
fellow researchers found mice lacking the MBD4 enzyme are up to three times
more likely to have genetic mutations. Authors of the study conclude,
"These findings suggest that human MBD4 plays a similarly important role
in reducing inherited disease and cancer."
Use
of Iscador, an extract of European mistletoe (Viscum album), in cancer
treatment: prospective nonrandomized and randomized matched-pair studies nested
within a cohort study. Grossarth-Maticek R, Kiene H, Baumgartner SM, Ziegler R.
http://www.ncbi.nlm.nih.gov/pubmed/11347286
Source
Institute for Preventive Medicine, European Center for Peace and Development, United Nations, Heidelberg, Germany.
Abstract
CONTEXT:
In anthroposophical medicine, total extracts of Viscum album (mistletoe) have been developed to treat cancer patients. The oldest such product is Iscador. Although Iscador is regarded as a complementary cancer therapy, it is the most commonly used oncological drug in Germany.
OBJECTIVE:
To determine whether Iscador treatment prolongs survival time of patients with carcinoma of the colon, rectum, or stomach; breast carcinoma with or without axillary or remote metastases; or small cell or non-small-cell bronchogenic carcinoma; and to explore synergies between Iscador treatment and psychosomatic self-regulation.
DESIGN:
Prospective nonrandomized and randomized matched-pair studies nested within a cohort study.
SETTING:
General community in Germany.
PARTICIPANTS:
10,226 cancer patients involved in a
prospective long-term epidemiological cohort study, including 1668 patients
treated with Iscador and 8475 who had taken neither Iscador nor any other
mistletoe product (control patients).
INTERVENTION:
Iscador.
MAIN OUTCOME
MEASURE:
Survival time.
RESULTS:
In the nonrandomized matched-pair study, survival time
of patients treated with Iscador was longer for all types of cancer studied.
In the pool of 396 matched pairs, mean survival time in the Iscador groups
(4.23 years) was roughly 40% longer than in the control groups (3.05
years; P < .001). Synergies between Iscador treatment and self-regulation
manifested in a longer survival advantage for Iscador patients with good
self-regulation (56% relative to control group; P = .03) than for patients with
poor self-regulation. Results of the 2 randomized matched-pair studies largely
confirmed the results of the non-randomized studies.
CONCLUSION:
Iscador treatment can achieve a clinically relevant prolongation of survival time of cancer patients and appears to stimulate self-regulation.
Iscador
9.9.10: Please read this “new to us”article on Iscador
I often treat cancer with Iscador, an
alternative and nontoxic therapy made from a lacto-fermented extract of
mistletoe (Viscum album L.)
This treatment is one of the most extensively studied complementary medical
therapies, particularly in Europe where it has been used as an adjunctive
therapy for solid tumor cancers. An early 2005 study confirms the safety of
complementary Iscador therapy in patients with high-risk melanoma. Equally
important, the Iscador users had a significantly improved length and quality of
survival and fewer distant metastasis than those who didn’t use Iscador. See
below to link to the abstract or download a Booklet (PDF format)
about the study.
Because I like to provide information to
people to help them better understand their conditions and their options, I
have included below a selection of papers, studies and trials that have been
conducted using mistletoe extract therapy. Click on the link at Abstract to
read the full abstract at the National Center for Biotechnology Information’s
National Library of Medicine website, www.ncbi.nlm.nih.gov.
At the bottom of this page, I also include several other websites with
additional information and links on Iscador and cancer therapy.
I have had numerous requests from patients
who are undergoing treatment for cancer, particularly Iscador therapy, who
would like to talk with other patients about their experiences. We want to act
as a conduit to put people in touch with one another so they can get more
information and share stories. The focus of this discussion forum is on patients and their
experiences. It will be wholly the effort of those who have an interest. I will
not be involved in any way except as the initial facilitator for putting people
together through a confidential email exchange.
Please note that this material is intended for informational and educational purposes only and is not intended to replace consultation with a doctor.
Selected Papers Abstracts
link to NCBI’s National Library of Medicine PubMed site
|
[Safety
and efficacy of the long-term adjuvant treatment of primary intermediate- to
high-risk malignant melanoma (UICC/AJCC stage II and III) with a standardized
fermented European mistletoe (Viscum album L.) extract. Results from a
multicenter, comparative, epidemiological cohort study in Germany and
Switzerland.]Augustin M, Bock PR, Hanisch J, Karasmann M,
Schneider B Department of Dermatology, University Hospital, University of
Freiburg, Freiburg/Brsg (Germany) Arzneimittelforschung.
2005;55(1):38-49. Abstract
Booklet(PDF
format)
The
objective of the study was to evaluate the safety and therapeutic efficacy of
a long-term mistletoe therapy with Iscador within the scope of post-operative
treatment in patients with mean- to high-risk primary malignant melanoma by
comparison with a untreated parallel control group. Conclusion: a long-term
Iscador treatment in patients with mean- to high-risk primary malignant
melanoma appears to be safe.PMID: 15727163 |
[Efficacy
and safety of long-term complementary treatment with standardized European
mistletoe extract (Viscum album L.) in addition to the conventional adjuvant
oncologic therapy in patients with primary non-metastasized mammary
carcinoma. Results of a multi-center, comparative, epidemiological cohort
study in Germany and Switzerland] [Article in German]Bock
PR, Friedel WE, Hanisch J, Karasmann M, Schneider B. Institut fur Angewandte
Gesundheitsforschung, IFAG Basel AG, Basel, Schweiz.Arzneimittelforschung.
2004;54(8):456-66. Abstract
Booklet
(PDF format)
A
study to evaluate the therapeutic efficacy and safety of long-term
complementary therapy in primary, non-metastatic mammary carcinoma patients
in UICC stage I-III with a standardized European mistletoe extract given in
addition to conventional adjuvant oncologic therapy.Publication Types: Clinical Trial, Multicenter Study, Randomized Controlled Trial PMID: 15460213 |
Impact of complementary
mistletoe extract treatment on quality of life in breast, ovarian and
non-small cell lung cancer patients. A prospective randomized controlled
clinical trial.Piao BK, Wang YX, Xie GR,
Mansmann U, Matthes H, Beuth J, Lin HS. Guang An Men Hospital, Beijing,
China.
Anticancer
Res.
2004 Jan-Feb;24(1):303-9.Abstract This study showed that complementary treatment with sME can beneficially reduce the side-effects of chemotherapy in cancer patients and thus improve quality of life. Publication Types: Clinical Trial, Multicenter Study, Randomized Controlled Trial PMID: 15015612 |
Differential effects of
Viscum album extract Iscador(R)Qu on cell cycle progression and apoptosis in
cancer cells.Harmsma M, Gromme M,
Ummelen M, Dignef W, Tusenius KJ, Ramaekers FC. Department of Molecular Cell
Biology, University of Maastricht, 6200 MD Maastricht, The Netherlands.
Int
J Oncol.
2004 Dec;25(6):1521-9. Abstract This study
tested the hypothesis that Iscador(R)Qu, an aqueous fermented extract from
the European mistletoe grown on oaks, induces tumor regression by cell cycle
inhibition and/or interference with apoptotic signaling pathways in cancer
cells. PMID: 15547686 |
Critical role of reactive
oxygen species and mitochondrial membrane potential in korean mistletoe
lectin-induced apoptosis in human hepatocarcinoma cells.Kim
WH, Park WB, Gao B, Jung MH. Division of Metabolic Disease, Department of Biomedical
Science, National Institutes of Health, #5 Nokbun-dong, Eunpyung-gu, Seoul
122-701, South Korea.
Mol
Pharmacol. 2004 Dec;66(6):1383-96. Epub 2004 Aug 31.Abstract Viscum album L. coloratum agglutinin (VCA), isolated from Korean mistletoe, is a strong inducer of apoptosis in a variety of tumor cells; however, the underlying molecular mechanisms responsible are not clear. This study shows that VCA induces apoptotic killing. PMID: 15340045 |
Influence of postoperative
complementary treatment with lectin-standardized mistletoe extract on breast
cancer patients. A controlled epidemiological multicentric retrolective
cohort study. Schumacher K, Schneider
B, Reich G, Stiefel T, Stoll G, Bock PR, Hanisch J, Beuth J. Institut fuer
Biometrie, Medizinische Hochschule Hannover, Konstanty-Gutschow-Str. 8, 30625
Hannover, Germany.
Anticancer
Res.
2003 No v-Dec;23(6D):5081-7.Abstract This epidemiological study was performed to evaluate the influence of postoperative complementary treatment with lectin-standardized mistletoe extract (sME) on breast cancer patients. Publication Types: Clinical Trial, Multicenter Study, Randomized Controlled Trial PMID: 14981970 |
Mistletoe and gemcitabine
in patients with advanced cancer: a model for the phase I study of botanicals
and botanical-drug interactions in cancer therapy.
Mansky PJ, Grem J, Wallerstedt DB, Monahan BP, Blackman MR. National Center
for Complementary and Alternative Medicine, National Institutes of Health,
Bethesda, MD 20892-2669, USA
Integr
Cancer Ther. 2003 Dec;2(4):345-52.Abstract While the clinical efficacy of mistletoe in cancer is being investigated, toxicity and potential interactions of mistletoe with standard chemotherapeutic agents are unknown. PMID: 14713326 |
Phase II study of viscum
fraxini-2 in patients with advanced hepatocellular carcinoma.Mabed
M, El-Helw L, Shamaa S. Hematology and Medical Oncology Unit, Faculty of
Medicine, Mansoura University, Mansoura, Egypt
Br
J Cancer. 2004 Jan 12;90(1):65-9.Abstract This study was conducted to evaluate the efficacy and safety of viscum fraxini-2 in patients with chemotherapy-naive, advanced hepatocellular carcinoma. Publication Types: Clinical Trial; Clinical Trial, Phase II PMID: 14710208 |
The influence of isorel on
the advanced colorectal cancer.Cazacu
M, Oniu T, Lungoci C, Mihailov A, Cipak A, Klinger R, Weiss T, Zarkovic N.
The 4th Surgical Clinic–University of Medicine and Pharmacy Iuliu Hatieganu,
Romania.
Cancer
Biother Radiopharm. 2003 Feb;18(1):27-34.Abstract A study of a therapeutical approach of surgery and chemotherapy combined with biotherapy by Viscum album extract Isorel, aiming to improve the patients’ resistance to the disease and to render the treatment’s side effects more tolerable. Publication Types: Clinical Trial, Randomized Controlled Trial PMID: 12667306 |
[Blood
and tissue eosinophilia, mistletoe lectin antibodies and quality of life in a
breast cancer patient undergoing intratumoral and subcutaneous mistletoe
therapy] [Article in German]Kroz M, Schad F, Matthes B,
Pickartz H, Girke M. Forschungsinstitut Havelhohe am Gemeinschaftskrankenhaus
Havelhohe, Germany.
Forsch
Komplementarmed Klass Naturheilkd. 2002
Jun;9(3):160-7.Abstract Study of Mistletoe therapy (MT) as a method of complementary medicine, using high-dose intratumoral application. Publication Types: Case Reports PMID: 12119512 |
Mistletoe viscotoxins
increase natural killer cell-mediated cytotoxicity.
Tabiasco J, Pont F, Fournie JJ, Vercellone A. Institut National de la Sante
et de la Recherche Medicale U563 and Service de spectrometrie de masse de l’
IFR 30, CHU Purpan, BP3028, Toulouse, France.
Eur
J Biochem. 2002 May;269(10):2591-600. Abstract Study to
show that nontoxic concentrations of Viscum album extracts increase natural
killer (NK) cell-mediated killing of tumor cells but spare nontarget cells
from NK lysis. PMID: 12027898 |
Induction of apoptosis of
endothelial cells by Viscum album: a role for anti-tumoral properties of
mistletoe lectins.Van Huyen JP, Bayry J,
Delignat S, Gaston AT, Michel O, Bruneval P, Kazatchkine MD, Nicoletti A,
Kaveri SV. INSERM U430, Hopital Broussais, Paris, France.
Mol
Med.
2002 Oct;8(10):600-6.Abstract Study that tests the hypothesis that VA extracts induce endothelial cell death and apoptosis. PMID: 12477970 |
[Frequency
of the common cold in healthy subjects during exposure to a lectin-rich and a
lectin-poor mistletoe preparation in a randomized, double-blind,
placebo-controlled study] [Article in German]Huber R,
Klein R, Ludtke R, Werner M. Ambulanz fur Naturheilverfahren/Abteilung Innere
Medizin II, Universitatsklinikum Freiburg i.Br.
Forsch
Komplementarmed Klass Naturheilkd. 2001
Dec;8(6):354-8.Abstract Mistletoe preparations have immunomodulatory properties in vitro and in vivo. This study investigates whether or not these properties have an effect on the frequency of the common cold in healthy subjects. Publication Types: Clinical Trial, Randomized Controlled Trial PMID: 11799303 |
Use of Iscador, an extract
of European mistletoe (Viscum album), in cancer treatment: prospective
nonrandomized and randomized matched-pair studies nested within a cohort
study.Grossarth-Maticek R, Kiene
H, Baumgartner SM, Ziegler R. Institute for Preventive Medicine, European
Center for Peace and Development, United Nations, Heidelberg, Germany.
Altern
Ther Health Med. 2001 May-Jun;7(3):57-66, 68-72, 74-6
passim.Abstract Study to determine whether Iscador treatment prolongs survival time of patients with carcinomas and to explore synergies between Iscador treatment and psychosomatic self-regulation. Publication Types: Clinical Trial, Multicenter Study, Randomized Controlled Trial PMID: 11347286 |
Potentiation of tumor
necrosis factor-alpha-induced apoptosis by mistletoe lectin.Pae
HO, Seo WG, Oh GS, Shin MK, Lee HS, Lee HS, Kim SB, Chung HT. Department of
Microbiology and Immunology, Wonkwang University School of Medicine, Iksan,
Korea. Immunopharmacol
Immunotoxicol. 2000 Nov;22(4):697-709.
Abstract Mistletoe
lectins (MLs) constitute the active principle in extract preparations from
mistletoe, commonly used as immunomodulator in adjuvant tumor therapy. PMID: 11105782 |
[Mistletoe
extracts in the therapy of malignant, hematological and lymphatic diseases--a
monocentric, retrospective analysis over 16 years]
[Article in German] Stumpf C, Rosenberger A, Rieger S, Troger W, Schietzel M. Forsch Komplementarmed
Klass Naturheilkd. Krebsforschung
Herdecke e.V., Gemeinschaftskrankenhaus Herdecke. 2000
Jun;7(3):139-46.
Abstract A study to
investigate potentials risks of treatment with mistletoe extracts in patients
with malignant haematological and lymphatic diseases. PMID: 10899748 |
Activation of c-Jun
N-terminal kinase 1 (JNK1) in mistletoe lectin II-induced apoptosis of human
myeloleukemic U937 cells.
Park R, Kim MS, So HS, Jung BH, Moon SR, Chung SY, Ko CB, Kim BR, Chung HT.
Department of Microbiology, Professional Graduate School of Oriental
Medicine, Wonkwang University School of Medicine, 570-749, Iksan Chonbuk,
South Korea. Biochem
Pharmacol. 2000 Dec 1;60(11):1685-91.
Abstract Study of
extracts of mistletoe (Viscum album var. coloratum) and the mechanism by
which the plant extracts kill tumor cells has remained elusive. PMID: 11077051 |
Biological effects of
natural and recombinant mistletoe lectin and an aqueous mistletoe extract on
human monocytes and lymphocytes in vitro.
Elsasser-Beile U, Voss M, Schuhle R, Wetterauer U. Department of Urology,
University of Freiburg, Germany.Clin
Lab Anal. 2000;14(6):255-9.
Abstract A study to
compares the immunological potency of different well-defined mistletoe lectin
preparations on human immune cells. PMID: 11138605 |
Hypereosinophilia induced
by high-dose intratumoral and peritumoral mistletoe application to a patient
with pancreatic carcinoma.
Huber R, Barth H, Schmitt-Graff A, Klein R. Center for Complementary
Medicine, Department of Gastroenterology, University of Freiburg, Germany.J Altern Complement Med.
2000 Aug;6(4):305-10.
Abstract Study of a
patient with inoperable adenocarcinoma of the pancreas treated with
intraperitumoral and peritumoral injections of a mistletoe extract. Publication Types: Case Reports PMID: 10976976 |
Antitumoral effects of an
intravesically applied aqueous mistletoe extract on urinary bladder carcinoma
MB49 in mice. Mengs U, Schwarz T,
Bulitta M, Weber K. Madaus AG, Ostmerheimer Strasse 198, D-51109 Koln,
Germany.Anticancer Res.
2000 Sep- Oct;20(5B):3565-8.
Abstract Study to
investigate the effects of a locally applied aqueous mistletoe extract on the
growth of urinary bladder carcinoma. PMID: 11131663 |
Tolerability of an extract
of European mistletoe among immunocompromised and healthy individuals. Gorter
RW, van Wely M, Reif M, Stoss M. University of California, San Francisco,
USA. Altern Ther Health
Med. 1999 Nov;5(6):37-44, 47-8.
AbstractStudy to determine the toxicity profile and biochemical effects of a Viscum album extract. Publication Types: Clinical Trial, Review, Tutorial PMID: 10550904 |
Insulin-secreting activity
of the traditional antidiabetic plant Viscum album (mistletoe).
Gray AM, Flatt PR. School of Biomedical Sciences, University of Ulster,
Coleraine, Northern Ireland BT52 1SA, UK. J
Endocrinol. 1999 Mar;160(3):409-14.
AbstractStudy of effects and presence of insulin-releasing natural product(s) in Viscum album which may contribute to the reported antidiabetic property of the plant. PMID: 10076186 |
[Mistletoe
therapy from the pharmacologic perspective] [Article in
German] Hajto T, Hostanska K, Saller R. Abteilung Naturheilkunde, Departement
Innere Medizin, Universitatsspital Zurich, Schweiz. Forsch Komplementarmed.
1999 Aug;6(4):186-94.
AbstractStudy of experimental data that suggest that the mistletoe lectins Viscum album agglutinin (VAA)-I and -II are play an important role in the efficacy of mistletoe therapy. Publication Types: Review, Academic Review PMID: 10529578 |
[Iscador
QuS and human recombinant interferon alpha (Intron A) in cervical
intraepithelial neoplasia (CIN)] [Article in Polish] Jach
R, Basta A. Katedry i Kliniki Ginekologii i Onkologii Collegium Medicum
Uniwersytetu Jagiellonskiego w Krakowie. Przegl
Lek. 1999;56(1):86-8 Abstract
The
aim of this work was the evaluation of the Iscador QuS and Intron A role in
the management of HPV associated CIN. Publication Types: Clinical Trial, Controlled Clinical Trial PMID: 10375935 |
Direct and rapid induction
of migration in human CD4+ T lymphocytes within three-dimensional collagen
matrices mediated by signalling via CD3 and/or CD2.
Nikolai G, Niggemann B, Werner M, Zanker KS, Friedl P. Institute of
Immunology, University of Witten/Herdecke, D-58448 Witten, Germany. Immunology. 1998
Sep;95(1):62-8.
AbstractStudy of specific activation of T cells which require stable cell-cell interaction; however, little is known how the transition from a previously motile state into a sessile state following activation is achieved. PMID: 9767458 |
[What prospects of success
does Iscador therapy offer in advanced ovarian cancer?]
[Article in German] Hassauer W, Gutsch J, Burkhardt R. Onkologie. 1979
Feb;2(1):28-36. Abstract
A
study of the carcinostatic effect of Iscador in the treatment of carcinoma of
the ovary. Publication Types: Clinical Trial PMID: 392367 |
[Investigation to improve
the survival of patients with bronchial carcinomas "radically operated"
(author's transl)] [Article in German]
Salzer G.Z Erkr
Atmungsorgane. 1975 Feb;142(2):127-31. Abstract
Postoperative
treatment (using Iscador) of patients with successfully resected bronchial
carcinoma is described. PMID: 1226878 |
Weleda’s website has useful information on their product, Iscador, including information on published data and articles.
The Townsend Letter for Doctors and Patients (October 2002)
Article on Mistletoe Extracts & Cancer Therapy[Mistletoe (Viscum album) preparations: an optional drug for cancer patients?]
[Article in Hebrew] Bar-Sela G, Gershony A, Haim N. Department of Oncology, Rambam
Medical Center and Faculty of Medicine, Technion-Israel Institute of
Technology, Haifa, Israel. g_barsela@rambam.health.gov.il Extracts and
preparations from the parasitic plant mistletoe (Viscum album L.) have been
used in the treatment of cancer for decades. Mistletoe treatment for cancer was
introduced in 1920 by Steiner and Wegman, founders of the Anthroposophical
medical method. Today, mistletoe extracts are the most frequently prescribed
unconventional cancer therapies in Germany, as in some other European
countries. Full clinical data about the efficacy of the mistletoe preparations
is still missing. The preparations are usually given as subcutaneous
injections, but other routes of administration are also used. Numerous
preclinical and in-vitro studies have reported immunostimulatory, cytotoxic and
proapoptotic effects. More than 15 prospective clinical trials using mistletoe
extracts in patients with different malignancies have been reported. In most of
these studies the authors reported that mistletoe extracts had therapeutic
benefit in terms of response rate, overall survival, quality of life and
reduction in side-effects of the oncological treatment. Unfortunately, almost
all of these reported studies had at least one major weakness that questioned
their reliability. Side effects of the different mistletoe preparation used
in human studies are generally minimal and non-life threatening. In the current
review recent studies, including two phase II studies from our center, are
included. In the future, data that will be obtained from good quality studies
might facilitate reaching firm conclusions regarding the therapeutic benefit of
mistletoe preparation for oncological treatment.
Mistletoe
http://depts.washington.edu/integonc/clinicians/act/mistletoe.shtml
Mistletoe is widely prescribed immune
therapy used in treating cancer patients in Europe both as concurrent therapy
with chemotherapy and as adjuvant treatment. Subcutaneous injections of
mistletoe lectins have been studied in over 25 cancer clinical trials in
Europe, Russia and other countries, but thus far not in the U.S. The bulk of
the data suggests anti-tumor activity across several tumor types. In Europe,
mistletoe remains one the most extensively studied herbal preparations with
over 1,000 published scientific articles. Mistletoe products are sold as
Iscador, Helixor, Abnoba viscum, Isorel, Eurixor, and Plenosol. Preclinical
studies have shown cytotoxic, carcinostatic and immunomodulatory effects both
in vitro and in vivo on a variety of tumor cells. Clinical studies have also
shown cytotoxic effects of mistletoe over various tumor types. Most of these
studies report improvements in response, survival and/or 'quality of life'
although many of these reports were of less than ideal designs (i.e. small
studies, lack of randomization or lack of appropriate assessment of clinical
improvement).
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