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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1995-5-11
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pubmed:abstractText |
Targeted delivery of macrophage activating agents is an attractive approach to treat micrometastatic disease. Liposome-encapsulated muramyl tripeptide phosphatidylethanolamine (L-MTP-PE) is a potent activator of monocytes/macrophages in humans, mice, and dogs. We have conducted clinical trials in dogs with malignant and highly metastatic spontaneous tumors. Presented are results of our trials evaluating L-MTP-PE in combination with surgery and chemotherapy in dogs with spontaneous osteosarcoma and hemangiosarcoma, particularly relevant malignancies having having many similarities to human cancer. Osteosarcoma dogs received chemotherapy following surgery (cisplatin q 28 days x 4). At completion of chemotherapy, dogs were randomized to receive L-MTP-PE or placebo. The L-MTP-PE group had a significantly longer median survival time compared to the placebo group (p < 0.021). Dogs with splenic hemangiosarcoma received combination chemotherapy following surgery (doxorubicin and cyclophosphamide q 21 days x 4). At the first chemotherapy, dogs were randomized to receive L-MTP-PE or placebo. The L-MTP-PE group had a significantly longer median survival time compared to the placebo group (p < 0.03). These studies show that L-MTP-PE is an effective agent for treatment of metastasis and can be safely administered in combination with chemotherapy.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acetylmuramyl-Alanyl-Isoglutamine,
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Cisplatin,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclophosphamide,
http://linkedlifedata.com/resource/pubmed/chemical/Doxorubicin,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylethanolamines,
http://linkedlifedata.com/resource/pubmed/chemical/muramylNAc-Ala-isoGln-Lys-tripeptide...
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pubmed:status |
MEDLINE
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pubmed:issn |
1061-186X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
2
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pubmed:owner |
NLM
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pubmed:authorsComplete |
N
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pubmed:pagination |
391-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7704483-Acetylmuramyl-Alanyl-Isoglutamine,
pubmed-meshheading:7704483-Animals,
pubmed-meshheading:7704483-Antineoplastic Agents,
pubmed-meshheading:7704483-Bone Neoplasms,
pubmed-meshheading:7704483-Cisplatin,
pubmed-meshheading:7704483-Cyclophosphamide,
pubmed-meshheading:7704483-Dog Diseases,
pubmed-meshheading:7704483-Dogs,
pubmed-meshheading:7704483-Doxorubicin,
pubmed-meshheading:7704483-Hemangiosarcoma,
pubmed-meshheading:7704483-Lung Neoplasms,
pubmed-meshheading:7704483-Osteosarcoma,
pubmed-meshheading:7704483-Phosphatidylethanolamines,
pubmed-meshheading:7704483-Prospective Studies,
pubmed-meshheading:7704483-Splenic Neoplasms
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pubmed:year |
1994
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pubmed:articleTitle |
Current studies of liposome muramyl tripeptide (CGP 19835A lipid) therapy for metastasis in spontaneous tumors: a progress review.
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pubmed:affiliation |
Department of Medical Sciences, University of Wisconsin, Madison 53706.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Randomized Controlled Trial,
Research Support, Non-U.S. Gov't
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