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Chinese Journal of Oncology ; (12): 316-318, 2007.
Article in Chinese | WPRIM | ID: wpr-255654

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the safety and feasibility of dose dense chemotherapy in the postoperative adjuvant treatment for breast cancer.</p><p><b>METHODS</b>The data of 114 breast cancer patients treated with adjuvant dose dense chemotherapy was retrospectively analyzed.</p><p><b>RESULTS</b>114 breast cancer patients received postoperative adjuvant dose dense chemotherapy from Jan. 2004 to March 2005. The patients were treated with different regimens according to their recurrence risk: 43 with paclitaxel + epirubicin (PE), 8 with taxotere + epirubicin (TE), 36 with cyclophosphamide + epirubicin + 5-Fu ( CEF) and 27 with epirubicin +5-Fu (EC). Totally, 111 patients except 3 completed the dose dense chemotherapy smoothly. Major toxicities severer than grade III included: neutropenia in 6.3% of the patients, nausea and vomit in 11.7%, peripheral neuropathy in 3.6%.</p><p><b>CONCLUSION</b>Postoperative adjuvant dose dense chemotherapy for breast cancer patient is feasible and safe, but the long-term outcome still needs further observation.</p>


Subject(s)
Adult , Aged , Female , Humans , Middle Aged , Antineoplastic Combined Chemotherapy Protocols , Therapeutic Uses , Breast Neoplasms , Drug Therapy , Pathology , General Surgery , Chemotherapy, Adjuvant , Cyclophosphamide , Disease-Free Survival , Dose-Response Relationship, Drug , Epirubicin , Fluorouracil , Follow-Up Studies , Liver Neoplasms , Lymphatic Metastasis , Mastectomy , Methods , Nausea , Neutropenia , Paclitaxel , Postoperative Period , Retrospective Studies , Taxoids
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