Adjuvant Capecitabine With Docetaxel and Cyclophosphamide Plus Epirubicin for Triple-Negative Breast Cancer (CBCSG010): An Open-Label, Randomized, Multicenter, Phase III Trial

卡培他滨 医学 表阿霉素 多西紫杉醇 内科学 紫杉烷 蒽环类 肿瘤科 环磷酰胺 乳腺癌 中性粒细胞减少症 发热性中性粒细胞减少症 养生 外科 化疗 癌症 结直肠癌
作者
Junjie Li,Ke-Da Yu,Da Pang,Changqin Wang,Jun Jiang,Sheng Yang,Yunjiang Liu,Peifen Fu,Shengtao Yuan,Guo‐Jun Zhang,Yimei Cao,Qi He,Shude Cui,Xijing Wang,Guosheng Ren,Xinzheng Li,Shiyou Yu,Pengxi Liu,Xiang Qiu,Jinhai Tang,Ouchen Wang,Zhimin Fan,Guoqin Jiang,Jin Zhang,Jiandong Wang,Hongwei Zhang,Shui Wang,Jianguo Zhang,Feng Jin,Nanyan Rao,Binlin Ma,Ping He,Binghe Xu,Zhixiong Zhuang,Jianfeng Wang,Qiang Sun,Xiao-feng Guo,Miao Mo,Zhimin Shao
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:38 (16): 1774-1784 被引量:65
标识
DOI:10.1200/jco.19.02474
摘要

PURPOSE Standard adjuvant chemotherapy for triple-negative breast cancer (TNBC) includes a taxane and an anthracycline. Concomitant capecitabine may be beneficial, but robust data to support this are lacking. The efficacy and safety of the addition of capecitabine into the TNBC adjuvant treatment regimen was evaluated. PATIENTS AND METHODS This randomized, open-label, phase III trial was conducted in China. Eligible female patients with early TNBC after definitive surgery were randomly assigned (1:1) to either capecitabine (3 cycles of capecitabine and docetaxel followed by 3 cycles of capecitabine, epirubicin, and cyclophosphamide) or control treatment (3 cycles of docetaxel followed by 3 cycles of fluorouracil, epirubicin, and cyclophosphamide). Randomization was centralized without stratification. The primary end point was disease-free survival (DFS). RESULTS Between June 2012 and December 2013, 636 patients with TNBC were screened, and 585 were randomly assigned to treatment (control, 288; capecitabine, 297). Median follow-up was 67 months. The 5-year DFS rate was higher for capecitabine than for control treatment (86.3% v 80.4%; hazard ratio, 0.66; 95% CI, 0.44 to 0.99; P = .044). Five-year overall survival rates were numerically higher but not significantly improved (capecitabine, 93.3%; control, 90.7%). Overall, 39.1% of patients had capecitabine dose reductions, and 8.4% reported grade ≥ 3 hand-foot syndrome. The most common grade ≥ 3 hematologic toxicities were neutropenia (capecitabine, 136 [45.8%]; control, 118 [41.0%]) and febrile neutropenia (capecitabine, 50 [16.8%]; control, 46 [16.0%]). Safety data were similar to the known capecitabine safety profile and generally comparable between arms. CONCLUSION Capecitabine when added to 3 cycles of docetaxel followed by 3 cycles of a 3-drug anthracycline combination containing capecitabine instead of fluorouracil significantly improved DFS in TNBC without new safety concerns.
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