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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2 Suppl 4
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pubmed:dateCreated |
1998-5-12
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pubmed:abstractText |
We have explored several novel high-dose combinations in an attempt to increase antitumor activity while decreasing treatment-related toxicity. From October 1989 through June 1997, we performed phase I/II dose-escalation trials exploring novel high-dose regimens including ifosfamide/carboplatin/etoposide, mitoxantrone/thiotepa, and paclitaxel (Taxol; Bristol-Myers Squibb Company, Princeton, NJ)/mitoxantrone/thiotepa. We have also evaluated busulfan/cyclophosphamide and cyclophosphamide/thiotepa/carboplatin in phase II trials. Three hundred ninety-three patients have been treated in these trials and followed for a minimum of 3 months. Event-free survival (including relapses and treatment-related mortality; +/-SE) at 3 years by stage and chemosensitivity is as follows: stage II, four to nine positive nodes (n=16), 52%+/-17%; stage II, greater than nine nodes (n=30), 46%+/-11%; stage III (n=59), 50%+/-8%; inflammatory stage III (n=15), 27%+/-17%; stage IV, anthracycline responsive (n=69), 19%+/-5%; stage IV, anthracycline refractory but responsive to salvage therapy with ifosfamide, carboplatin, and etoposide or paclitaxel (n=53), 12%+/-6%; stage IV, refractory (n=128), 5%+/-2%; and stage IV, not evaluable for response (n=23), 10%+/-8%. Treatment-related mortality was 4% for both phase I and II studies involving stage II breast cancer patients, 5% for stage III breast cancer, 15% for inflammatory breast cancer, and 18% for all stage IV breast cancers, responsive and refractory. We conclude that high-dose therapy for the treatment of high-risk early stage breast cancer or metastatic breast cancer results in durable remissions. Chemosensitivity to induction regimens remains the most important prognostic indicator, although long-term survival has been seen even in patients with highly refractory disease. Further studies are necessary to define optimal high-dose strategies based on stage and chemosensitivity of disease.
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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/Carboplatin,
http://linkedlifedata.com/resource/pubmed/chemical/Etoposide,
http://linkedlifedata.com/resource/pubmed/chemical/Ifosfamide,
http://linkedlifedata.com/resource/pubmed/chemical/Mitoxantrone,
http://linkedlifedata.com/resource/pubmed/chemical/Paclitaxel,
http://linkedlifedata.com/resource/pubmed/chemical/Taxoids,
http://linkedlifedata.com/resource/pubmed/chemical/Thiotepa
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0093-7754
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
25
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1-6; discussion 45-8
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:9578055-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:9578055-Breast Neoplasms,
pubmed-meshheading:9578055-Carboplatin,
pubmed-meshheading:9578055-Clinical Trials as Topic,
pubmed-meshheading:9578055-Disease-Free Survival,
pubmed-meshheading:9578055-Etoposide,
pubmed-meshheading:9578055-Female,
pubmed-meshheading:9578055-Humans,
pubmed-meshheading:9578055-Ifosfamide,
pubmed-meshheading:9578055-Mitoxantrone,
pubmed-meshheading:9578055-Neoplasm Staging,
pubmed-meshheading:9578055-Paclitaxel,
pubmed-meshheading:9578055-Taxoids,
pubmed-meshheading:9578055-Thiotepa
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pubmed:year |
1998
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pubmed:articleTitle |
Defining the role of novel high-dose chemotherapy regimens for the treatment of high-risk breast cancer.
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pubmed:affiliation |
Division of Bone Marrow Transplantation, University of South Florida, Tampa, USA.
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pubmed:publicationType |
Journal Article,
Review,
Research Support, Non-U.S. Gov't
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