Efficacy of epirubicin plus docetaxel or paclitaxel in the treatment of breast cancer

被引:1
作者
Zhu, Chen [1 ]
Gan, Pan-pan [1 ]
Sun, Na-lin [1 ]
Cao, Li-qun [1 ]
机构
[1] First Peoples Hosp Anqing, Oncol Dept, Anqing, Anhui, Peoples R China
关键词
Epirubicin; Docetaxel; Paclitaxel; Breast cancer; Adverse effects; NAB-PACLITAXEL; CHEMOTHERAPY;
D O I
10.4314/tjpr.v22i4.20
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: To determine the clinical efficacy of epirubicin plus docetaxel or paclitaxel in the management of breast cancer. Methods: This study was a randomized controlled trial that recruited 78 patients with breast cancer treated in The First People's Hospital of Anqing between December 2018 and March 2021. The participants were randomized to receive either epirubicin plus docetaxel (control group) or epirubicin plus paclitaxel (study group), with 39 cases in each group. Clinical outcomes, adverse events, quality of life, and prognosis of the two groups were compared. Results: Epirubicin plus paclitaxel produced greater efficacy than epirubicin plus docetaxel (p < 0.05). The combination also exhibited a higher safety profile versus epirubicin with docetaxel, as evidenced by lower incidences of nausea and vomiting, intestinal discomfort, muscle pain, and dyspnea reactions (p < 0.05). Epirubicin with paclitaxel resulted in greater improvement in quality of life in patients than epirubicin plus docetaxel (p < 0.05) as well as provided more benefits in terms of survival and recurrence control than epirubicin plus docetaxel (p < 0.05). Conclusion: Epirubicin/paclitaxel combination alleviates clinical symptoms, reduces adverse events, enhances patient prognosis, lowers the risk of postoperative recurrence, and provides superior quality of life when compared to epirubicin/docetaxel combination in breast cancer patients. Nonetheless, large-scale and better-randomized clinical trials are required to validate the findings of this study.
引用
收藏
页码:865 / 871
页数:7
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