Source:http://linkedlifedata.com/resource/pubmed/id/20658263
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2010-8-11
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pubmed:abstractText |
nab-Paclitaxel has shown favorable efficacy and toxicity profiles compared to other taxanes in the treatment of metastatic breast cancer. In this pilot trial, we evaluated a nab-paclitaxel-containing adjuvant regimen in patients with early stage breast cancer. Patients with node-positive or high-risk node-negative early-stage breast cancer were eligible following completion of standard primary therapy. All the patients received four cycles, at 21-day intervals, of nab-paclitaxel (100 mg/m(2) IV days 1, 8, and 15) and cyclophosphamide (600 mg/m(2) IV day 1). HER2-positive patients also received trastuzumab 8 mg/kg IV on cycle 1 day 1, followed by 6 mg/kg every 21 days for a total of 52 weeks. The purpose of this trial was to evaluate feasibility and toxicity of this nab-paclitaxel-containing adjuvant regimen. 62 patients were treated between 2/08 and 11/08. The majority of the patients (87%) were HER2-negative. This adjuvant regimen was well tolerated, and full doses of all agents were administered in >90% of cycles. Grade 3/4 neutropenia occurred in 53% of the patients; however, only one episode of febrile neutropenia occurred in a total of 249 cycles administered. Other grade 3/4 adverse events occurred in less than 5% of patients. After short follow-up, all the patients remain alive and disease-free. The combination of nab-paclitaxel and cyclophosphamide, with or without trastuzumab, is feasible and well tolerated in patients with early stage breast cancer. Further investigation of the role of nab-paclitaxel in adjuvant breast cancer therapy is indicated, but definitive evaluation will require randomized phase III trials.
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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/130-nm albumin-bound paclitaxel,
http://linkedlifedata.com/resource/pubmed/chemical/Albumins,
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal, Humanized,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclophosphamide,
http://linkedlifedata.com/resource/pubmed/chemical/HER2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Paclitaxel,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, erbB-2,
http://linkedlifedata.com/resource/pubmed/chemical/trastuzumab
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1573-7217
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
123
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
471-5
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:20658263-Adult,
pubmed-meshheading:20658263-Aged,
pubmed-meshheading:20658263-Albumins,
pubmed-meshheading:20658263-Antibodies, Monoclonal,
pubmed-meshheading:20658263-Antibodies, Monoclonal, Humanized,
pubmed-meshheading:20658263-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:20658263-Breast Neoplasms,
pubmed-meshheading:20658263-Chemotherapy, Adjuvant,
pubmed-meshheading:20658263-Cyclophosphamide,
pubmed-meshheading:20658263-Disease-Free Survival,
pubmed-meshheading:20658263-Drug Administration Schedule,
pubmed-meshheading:20658263-Feasibility Studies,
pubmed-meshheading:20658263-Female,
pubmed-meshheading:20658263-Humans,
pubmed-meshheading:20658263-Kaplan-Meier Estimate,
pubmed-meshheading:20658263-Lymphatic Metastasis,
pubmed-meshheading:20658263-Middle Aged,
pubmed-meshheading:20658263-Nanoparticles,
pubmed-meshheading:20658263-Neoplasm Staging,
pubmed-meshheading:20658263-Paclitaxel,
pubmed-meshheading:20658263-Pilot Projects,
pubmed-meshheading:20658263-Receptor, erbB-2,
pubmed-meshheading:20658263-Time Factors,
pubmed-meshheading:20658263-Treatment Outcome,
pubmed-meshheading:20658263-United States
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pubmed:year |
2010
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pubmed:articleTitle |
A pilot study of adjuvant nanoparticle albumin-bound (nab) paclitaxel and cyclophosphamide, with trastuzumab in HER2-positive patients, in the treatment of early-stage breast cancer.
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pubmed:affiliation |
Sarah Cannon Research Institute, 3322 West End Avenue Suite 900, Nashville, TN 37203, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Multicenter Study,
Clinical Trial, Phase II
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