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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2000-8-29
pubmed:abstractText
Our objective was to determine whether an immune response can be generated against MUC1 peptide and against tumor cell MUC1 after vaccination with MUC1-keyhole limpet hemocyanin (KLH) conjugate plus QS-21 in breast cancer patients. Nine patients with a history of breast cancer but without evidence of disease were treated with MUC1-KLH conjugate plus QS-21, containing 100 microg of MUC1 and 100 microg of QS-21. s.c. vaccinations were administered at weeks 1, 2, 3, 7, and 19. Peripheral blood was drawn at frequent intervals to assess antibody titers. Skin tests were placed at weeks 1, 3, 9, and 21 to determine delayed type hypersensitivity reactions. Common toxicities included a local skin reaction at the site of the vaccine, usually of 4-5 days' duration, and mild flu-like symptoms usually of 1-2 days' duration. High IgM and IgG antibody titers against synthetic MUC1 were detected. IgG antibody titers remain elevated from a minimum of 106-137 weeks after the first vaccination. Binding of IgM antibody to MCF-7 tumor cells was observed in seven patients, although there was minimal binding of IgG antibody. Two patients developed significant antibody titers post-high-dose chemotherapy and stem cell reinfusion. There was no evidence of T cell activation. This MUC1-KLH conjugate plus QS-21 was immunogenic and well tolerated in breast cancer patients. Additional trials are ongoing to determine the optimal MUC1 peptide for use in larger clinical trials. Further investigation of vaccine therapy in high-risk breast cancer is warranted.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1078-0432
pubmed:author
pubmed:issnType
Print
pubmed:volume
6
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1693-701
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:10815887-Adjuvants, Immunologic, pubmed-meshheading:10815887-Adult, pubmed-meshheading:10815887-Amino Acid Sequence, pubmed-meshheading:10815887-Antibodies, pubmed-meshheading:10815887-Breast Neoplasms, pubmed-meshheading:10815887-Cancer Vaccines, pubmed-meshheading:10815887-Diarrhea, pubmed-meshheading:10815887-Fatigue, pubmed-meshheading:10815887-Female, pubmed-meshheading:10815887-Fever, pubmed-meshheading:10815887-Headache, pubmed-meshheading:10815887-Hematologic Diseases, pubmed-meshheading:10815887-Hemocyanin, pubmed-meshheading:10815887-Humans, pubmed-meshheading:10815887-Immunoglobulin G, pubmed-meshheading:10815887-Immunoglobulin M, pubmed-meshheading:10815887-Middle Aged, pubmed-meshheading:10815887-Molecular Sequence Data, pubmed-meshheading:10815887-Mucin-1, pubmed-meshheading:10815887-Nausea, pubmed-meshheading:10815887-Neoplasm Staging, pubmed-meshheading:10815887-Peptide Fragments, pubmed-meshheading:10815887-Skin, pubmed-meshheading:10815887-Time Factors, pubmed-meshheading:10815887-Treatment Outcome, pubmed-meshheading:10815887-Tumor Cells, Cultured, pubmed-meshheading:10815887-Vaccination
pubmed:year
2000
pubmed:articleTitle
Vaccination of high-risk breast cancer patients with mucin-1 (MUC1) keyhole limpet hemocyanin conjugate plus QS-21.
pubmed:affiliation
Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
pubmed:publicationType
Journal Article, Clinical Trial, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't