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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1998-12-11
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pubmed:abstractText |
Forty-one patients with operable breast cancer and >/=10 positive axillary lymph nodes were treated with 6 cycles of dose-dense adjuvant chemotherapy consisting of epirubicin (100 mg/m2) every 2 weeks with G-CSF support. A total of 240 cycles were administered, all of them at full dose and 19 (8%) with a delay. Thirty-eight (93%) patients completed the treatment according to the protocol. The relative dose intensity of epirubicin was 0.99. Grade 3 toxicities included anemia (3%), nausea and vomiting (5%) and alopecia (71%). After a median follow-up of 40 months, 16 (39%) patients were free of relapse. In conclusion, the present study has shown that the administration of dose-dense chemotherapy with epirubicin is feasible in the adjuvant setting with minimal toxicity.
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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:issn |
0030-2414
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
55
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
508-12
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:9778614-Adult,
pubmed-meshheading:9778614-Aged,
pubmed-meshheading:9778614-Antibiotics, Antineoplastic,
pubmed-meshheading:9778614-Breast Neoplasms,
pubmed-meshheading:9778614-Combined Modality Therapy,
pubmed-meshheading:9778614-Dose-Response Relationship, Drug,
pubmed-meshheading:9778614-Drug Administration Schedule,
pubmed-meshheading:9778614-Epirubicin,
pubmed-meshheading:9778614-Feasibility Studies,
pubmed-meshheading:9778614-Female,
pubmed-meshheading:9778614-Follow-Up Studies,
pubmed-meshheading:9778614-Granulocyte Colony-Stimulating Factor,
pubmed-meshheading:9778614-Humans,
pubmed-meshheading:9778614-Lymphatic Metastasis,
pubmed-meshheading:9778614-Middle Aged
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pubmed:articleTitle |
Dose-dense adjuvant chemotherapy with epirubicin monotherapy in patients with operable breast cancer and >/=10 positive axillary lymph nodes. A feasibility study.
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pubmed:affiliation |
AHEPA Hospital, Aristotle University of Thessaloniki, Greece.
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pubmed:publicationType |
Journal Article,
Clinical Trial
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