Source:http://linkedlifedata.com/resource/pubmed/id/10516693
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
1999-12-27
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pubmed:abstractText |
Autologous peripheral blood stem cell transplantation following myeloablative chemotherapy is being increasingly utilized in the treatment of a variety of malignancies. We administered busulfan 16 mg/kg orally, thiotepa 500-700 mg/m2 i.v., and carboplatin 800-1000 mg/m2 i.v. to 56 women with metastatic carcinoma of the breast. Autologous peripheral blood stem cells, which had been collected after a combination of chemotherapy and granulocyte colony-stimulating factor, were infused on day 0. The major toxicities of the conditioning regimen included severe pancytopenia, stomatitis, nausea, emesis, diarrhea, fever, and infection. Transplant-related mortality was 1.8%. The incidence of opportunistic viral infections was 42.9%. Fourteen individuals achieved a complete response. The actuarial survival at 1223 days was 13.7% for the entire group of patients; the actuarial survival at 1009 days was 39.3% among complete responders. The functional status of the immune system was determined following transplantation in a subset of patients. Peripheral blood mononuclear cells were obtained before and after stem cell infusion, and were analyzed phenotypically and functionally. Proliferative and interleukin-2 synthetic ability of these cells was assessed following stimulation with phytohemagglutinin and anti-CD3 antibody. The response to influenza peptides was also ascertained. Proliferative and interleukin-2 synthetic capacity was markedly impaired for over a year. Memory response was virtually absent for up to 2 years following transplantation. The prolonged and marked immunosuppression following this myeloablative regimen was associated with a high incidence of opportunistic viral infections, and may have contributed to disease relapse and progression especially in patients who failed to achieve a complete response following transplantation.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0268-3369
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
24
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
837-43
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:10516693-Administration, Oral,
pubmed-meshheading:10516693-Adult,
pubmed-meshheading:10516693-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:10516693-Breast Neoplasms,
pubmed-meshheading:10516693-Busulfan,
pubmed-meshheading:10516693-Carboplatin,
pubmed-meshheading:10516693-Combined Modality Therapy,
pubmed-meshheading:10516693-Female,
pubmed-meshheading:10516693-Hematopoietic Stem Cell Transplantation,
pubmed-meshheading:10516693-Humans,
pubmed-meshheading:10516693-Middle Aged,
pubmed-meshheading:10516693-Myeloablative Agonists,
pubmed-meshheading:10516693-Neoplasm Metastasis,
pubmed-meshheading:10516693-Thiotepa,
pubmed-meshheading:10516693-Transplantation, Autologous,
pubmed-meshheading:10516693-Treatment Outcome
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pubmed:year |
1999
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pubmed:articleTitle |
Myeloablative chemotherapy with autologous peripheral blood stem cell transplantation for metastatic breast cancer: immunologic consequences affecting clinical outcome.
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pubmed:affiliation |
Department of Medicine, University of Connecticut School of Medicine, Farmington, CT 06030, USA.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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