Department of Medical Oncology, Dana Farber Cancer Institute, Boston, Massachusetts.
Department of Biostatistics, Mayo Clinic, Rochester, Minnesota.
JAMA. 2024 May 28;331(20):1714-1721. doi: 10.1001/jama.2024.4840.
Observational studies of survivors of breast cancer and prospective trials of aspirin for cardiovascular disease suggest improved breast cancer survival among aspirin users, but prospective studies of aspirin to prevent breast cancer recurrence are lacking.
To determine whether aspirin decreases the risk of invasive cancer events among survivors of breast cancer.
DESIGN, SETTING, AND PARTICIPANTS: A011502, a phase 3, randomized, placebo-controlled, double-blind trial conducted in the United States and Canada with 3020 participants who had high-risk nonmetastatic breast cancer, enrolled participants from 534 sites from January 6, 2017, through December 4, 2020, with follow-up to March 4, 2023.
Participants were randomized (stratified for hormone receptor status [positive vs negative], body mass index [≤30 vs >30], stage II vs III, and time since diagnosis [<18 vs ≥18 months]) to receive 300 mg of aspirin (n = 1510) or placebo once daily (n = 1510) for 5 years.
The primary outcome was invasive disease-free survival. Overall survival was a key secondary outcome.
A total of 3020 participants were randomized when the data and safety monitoring committee recommended suspending the study at the first interim analysis because the hazard ratio had crossed the prespecified futility bound. By median follow-up of 33.8 months (range, 0.1-72.6 months), 253 invasive disease-free survival events were observed (141 in the aspirin group and 112 in the placebo group), yielding a hazard ratio of 1.27 (95% CI, 0.99-1.63; P = .06). All invasive disease-free survival events, including death, invasive progression (both distant and locoregional), and new primary events, were numerically higher in the aspirin group, although the differences were not statistically significant. There was no difference in overall survival (hazard ratio, 1.19; 95% CI, 0.82-1.72). Rates of grades 3 and 4 adverse events were similar in both groups.
Among participants with high-risk nonmetastatic breast cancer, daily aspirin therapy did not improve risk of breast cancer recurrence or survival in early follow-up. Despite its promise and wide availability, aspirin should not be recommended as an adjuvant breast cancer treatment.
ClinicalTrials.gov Identifier: NCT02927249.
对乳腺癌幸存者的观察性研究和阿司匹林用于心血管疾病的前瞻性试验表明,阿司匹林使用者的乳腺癌生存率有所提高,但缺乏阿司匹林预防乳腺癌复发的前瞻性研究。
确定阿司匹林是否降低乳腺癌幸存者侵袭性癌症事件的风险。
设计、地点和参与者:A011502 是一项在美国和加拿大进行的 3 期、随机、安慰剂对照、双盲试验,共纳入 3020 名患有高危非转移性乳腺癌的患者,这些患者来自 534 个地点,招募时间为 2017 年 1 月 6 日至 2020 年 12 月 4 日,随访至 2023 年 3 月 4 日。
参与者被随机(按激素受体状态[阳性与阴性]、体重指数[≤30 与>30]、II 期与 III 期以及诊断后时间[<18 个月与≥18 个月]分层)接受每日 300 毫克阿司匹林(n=1510)或安慰剂(n=1510)治疗,为期 5 年。
主要结局是无侵袭性疾病生存。总生存是关键次要结局。
当数据和安全监测委员会建议在第一次中期分析时暂停研究时,共有 3020 名参与者被随机分组,因为风险比已经超过了预设的无效边界。中位随访 33.8 个月(范围,0.1-72.6 个月)时,观察到 253 例无侵袭性疾病生存事件(阿司匹林组 141 例,安慰剂组 112 例),风险比为 1.27(95%CI,0.99-1.63;P=0.06)。虽然阿司匹林组的所有无侵袭性疾病生存事件(包括死亡、侵袭性进展[远处和局部区域]和新原发事件)均呈数值升高趋势,但差异无统计学意义。总生存无差异(风险比,1.19;95%CI,0.82-1.72)。两组的 3 级和 4 级不良事件发生率相似。
在患有高危非转移性乳腺癌的患者中,每日阿司匹林治疗并不能降低早期随访中乳腺癌复发或生存的风险。尽管阿司匹林有希望且广泛可用,但不应推荐其作为辅助乳腺癌治疗。
ClinicalTrials.gov 标识符:NCT02927249。