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Comparison of Tamoxifen and Toremifene as Adjuvant Treatment in Node-negative Postmenopausal Breast Cancer
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KMID : 0371320020630040283
Abstract
Purpose: To evaluate the differences in therapeutic efficacy and toxicity profiles between adjuvant toremifene and tamoxifene in postmenopausal breast cancer patients.
Methods: Toremifene 40 §· (n=115) and tamoxifen 20 §· (n =116) were administered daily for more than 2 years after curative surgery for lymph node-negative breast cancer. Toxicity profiles were compared between the two groups and the
patient
survival rate was also analyzed.
Results: Sweating and hot flashes were the most common symptoms in the two groups (toremifene vs. tamoxifen= 47.8% vs. 49.1%). Increase of vaginal discharge (39.1% vs. 36.2%) and weight gain (21.7% vs. 24.1%) were the next following
adverse
effects. There was no significant difference in adverse effect between the two groups. During the median follow-up period of 25 months (range: 9¡38 months), five (4.3%) and four (3.3%) patients treated by toremifene and tamoxifen, respectively,
had
recurrent disease.
Conclusion: The clinical outcome and adverse effect profiles of toremifene were similar to those of tamoxifen. Toremifene at 40 §·/day seems to be as safe and effective as tamoxifen at 20 §·/day in the treatment of postmenopausal,
node-negative,
breast cancer. However, a longer follow-up study is needed to verify this.
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ºÎÀÛ¿ë; À¯¹æ¾Ï; Ä¡·á; Tamoxifen; Toremifen; Breast cancer; Side effect; Tamoxifen; Toremifene; Treatment;
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