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BMC Cancer ; 10: 281, 2010 Jun 11.
Article in English | MEDLINE | ID: mdl-20540745

ABSTRACT

BACKGROUND: The rates of chemotherapy-induced amenorrhea (CIA) associated with docetaxel-based regimens reported by previous studies are discordant. For navelbine-based chemotherapies, rates of CIA have seldom been reported. METHODS: Of 170 premenopausal patients recruited between January 2003 and September 2008, 78 were treated with fluorouracil plus epirubicin and cyclophosphamide (FEC), 66 were treated with docetaxel plus epirubicin (TE), and 26 were treated with navelbine plus epirubicin (NE). Patient follow-up was carried up every 3-4 months during the first year, then every 9-12 months during subsequent years. RESULTS: In univariate analysis, the rates of CIA were 44.87% for the FEC regimen, 30.30% for the TE regimen and 23.08% for the NE regimen (P = 0.068). Significant differences in the rates of CIA were not found between the FEC and TE treatment groups (P > 0.05), but were found between the FEC and NE treatment groups (P < 0.05). Furthermore, no significant differences were found between the TE and NE regimens (P > 0.05). Tamoxifen use was a significant predictor for CIA (P = 0.001), and age was also a significant predictor (P < 0.001). In multivariate analysis, age (P < 0.001), the type of chemotherapy regimens (P = 0.009) and tamoxifen use (P = 0.003) were all significant predictors. CONCLUSIONS: Age and administration of tamoxifen were found to be significant predictive factors of CIA, whereas docetaxel and navelbine based regimens were not associated with higher rates of CIA than epirubicin-based regimen.


Subject(s)
Amenorrhea/chemically induced , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Breast Neoplasms/drug therapy , Adult , Age Factors , Amenorrhea/epidemiology , Chemotherapy, Adjuvant , Cyclophosphamide/adverse effects , Docetaxel , Epirubicin/adverse effects , Female , Fertility/drug effects , Fluorouracil/adverse effects , Humans , Incidence , Logistic Models , Middle Aged , Odds Ratio , Retrospective Studies , Risk Assessment , Risk Factors , Tamoxifen/adverse effects , Taxoids/adverse effects , Time Factors , Treatment Outcome , Vinblastine/adverse effects , Vinblastine/analogs & derivatives , Vinorelbine , Young Adult
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