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Adjuvant chemotherapy for luminal A breast cancer: a prospective study comparing two popular chemotherapy regimens

机译:管腔A型乳腺癌的辅助化疗:一项前瞻性研究,比较了两种流行的化疗方案

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Introduction: Based on the variable benefit of taxanes in the adjuvant setting of early breast cancer in certain tumor phenotypes, especially in human epidermal growth factor receptor (HER)2-positive and triple-negative disease, and with the observation of a lesser benefit in luminal A, this research article aimed at exploring the value of docetaxel in patients with an estrogen receptor-positive, HER2-negative disease phenotype, who might not derive the same benefits as those with other phenotypes.Patients and methods: This was a randomized prospective study comparing disease-free survival (DFS) and safety profile of sequential adjuvant three cycles Fluorouracil, Epirubicin, Cyclophosphamide followed by three cycles Docetaxel (FEC-D) versus six cycles classic Fluorouracil, Epirubicin, Cyclophosphamide (FEC)-100 in 60 Egyptian women who presented to Dar Al Fouad Hospital during the period June 2007 to July 2008 with (pT1-2 pN0-3 M0). The primary end point was DFS in a follow-up period of 4 years. The secondary end point was toxicity profile.Results: Four-year DFS rates were comparable in both arms: 73.3% ± 8.1% in the FEC-D arm versus 76.5% ± 7.8% in the FEC-100 arm (P = 0.83). N3 and grade III subgroups achieved the worst DFS in both subgroups (P = 0.001 and P = 0.214, respectively). The rate of nausea and vomiting was higher in the FEC-100 arm (P = 0.49), while grade III–IV neutropenia and febrile neutropenia incidence was similar between both arms.Conclusion: Sequential adjuvant chemotherapy with FEC followed by docetaxel achieved comparable DFS results to FEC alone in luminal A phenotype subgroups of breast cancer.
机译:简介:基于紫杉烷类化合物在某些肿瘤表型,特别是在人类表皮生长因子受体(HER)2阳性和三阴性疾病中,在早期乳腺癌辅助治疗中的可变获益,并观察到在腔A,此研究文章旨在探讨多西他赛在雌激素受体阳性,HER2阴性疾病表型患者中的价值,这些患者可能无法获得与其他表型患者相同的益处。患者和方法:这是一项随机前瞻性研究研究在60名埃及妇女中比较了三周期氟尿嘧啶,表柔比星,环磷酰胺,三周期多西他赛(FEC-D)与六周期经典氟尿嘧啶,表柔比星,环磷酰胺(FEC)-100的顺序佐剂的无病生存期(DFS)和安全性概况在2007年6月至2008年7月期间以(pT1-2 pN0-3 M0)的身分到Dar Al Fouad医院就诊。主要终点是DFS,随访期为4年。结果:两组的四年DFS率相当:FEC-D组为73.3%±8.1%,而FEC-100组为76.5%±7.8%(P = 0.83)。在这两个亚组中,N3和III级亚组的DFS最差(分别为P = 0.001和P = 0.214)。 FEC-100组的恶心和呕吐率较高(P = 0.49),而两组间III–IV级中性粒细胞减少和发热性中性粒细胞减少的发生率相似。结论:先后用FEC联合多西他赛辅助化疗取得了可比的DFS结果在乳腺癌的管腔A表型亚组中单独应用FEC。

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