Effect of Capecitabine Maintenance Therapy Using Lower Dosage and Higher Frequency vs Observation on Disease-Free Survival Among Patients With Early-Stage Triple-Negative Breast Cancer Who Had Received Standard Treatment

医学 卡培他滨 乳腺癌 内科学 不利影响 四分位间距 三阴性乳腺癌 随机对照试验 肿瘤科 临床终点 辅助治疗 外科 癌症 结直肠癌
作者
Xi Wang,Shusen Wang,Heng Huang,Li Cai,Li Zhao,Roujun Peng,Ying Lin,Jun Tang,Jian Zeng,Lehong Zhang,Yongli Ke,Xianming Wang,Xin-Mei Liu,Qianjun Chen,Anqin Zhang,Fei Xu,Xiwen Bi,Jiajia Huang,Jibin Li,Danmei Pang,Cong Xue,Yanxia Shi,Zhen‐Yu He,Huan‐Xin Lin,Xin An,Wen Xia,Ye Cao,Ying Guo,Yanhong Su,Xin Hua,Xinyue Wang,Ruoxi Hong,Kuikui Jiang,Chenge Song,Zhangzan Huang,Shi Wei,Yong-Yi Zhong,Zhongyu Yuan
出处
期刊:JAMA [American Medical Association]
卷期号:325 (1): 50-50 被引量:153
标识
DOI:10.1001/jama.2020.23370
摘要

Among all subtypes of breast cancer, triple-negative breast cancer has a relatively high relapse rate and poor outcome after standard treatment. Effective strategies to reduce the risk of relapse and death are needed.To evaluate the efficacy and adverse effects of low-dose capecitabine maintenance after standard adjuvant chemotherapy in early-stage triple-negative breast cancer.Randomized clinical trial conducted at 13 academic centers and clinical sites in China from April 2010 to December 2016 and final date of follow-up was April 30, 2020. Patients (n = 443) had early-stage triple-negative breast cancer and had completed standard adjuvant chemotherapy.Eligible patients were randomized 1:1 to receive capecitabine (n = 222) at a dose of 650 mg/m2 twice a day by mouth for 1 year without interruption or to observation (n = 221) after completion of standard adjuvant chemotherapy.The primary end point was disease-free survival. Secondary end points included distant disease-free survival, overall survival, locoregional recurrence-free survival, and adverse events.Among 443 women who were randomized, 434 were included in the full analysis set (mean [SD] age, 46 [9.9] years; T1/T2 stage, 93.1%; node-negative, 61.8%) (98.0% completed the trial). After a median follow-up of 61 months (interquartile range, 44-82), 94 events were observed, including 38 events (37 recurrences and 32 deaths) in the capecitabine group and 56 events (56 recurrences and 40 deaths) in the observation group. The estimated 5-year disease-free survival was 82.8% in the capecitabine group and 73.0% in the observation group (hazard ratio [HR] for risk of recurrence or death, 0.64 [95% CI, 0.42-0.95]; P = .03). In the capecitabine group vs the observation group, the estimated 5-year distant disease-free survival was 85.8% vs 75.8% (HR for risk of distant metastasis or death, 0.60 [95% CI, 0.38-0.92]; P = .02), the estimated 5-year overall survival was 85.5% vs 81.3% (HR for risk of death, 0.75 [95% CI, 0.47-1.19]; P = .22), and the estimated 5-year locoregional recurrence-free survival was 85.0% vs 80.8% (HR for risk of locoregional recurrence or death, 0.72 [95% CI, 0.46-1.13]; P = .15). The most common capecitabine-related adverse event was hand-foot syndrome (45.2%), with 7.7% of patients experiencing a grade 3 event.Among women with early-stage triple-negative breast cancer who received standard adjuvant treatment, low-dose capecitabine maintenance therapy for 1 year, compared with observation, resulted in significantly improved 5-year disease-free survival.ClinicalTrials.gov Identifier: NCT01112826.
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