Borgquist Signe, Jensen Maj-Britt, Bendorff Cecilie Linea, Christiansen Peer, Offersen Birgitte Vrou, Kodahl Annette Raskov, Ewertz Marianne, Jensen Anders Bonde, Ahern Thomas P, Cronin-Fenton Deirdre, Ejlertsen Bent
Department of Oncology, Aarhus University Hospital/Aarhus University, Aarhus, Denmark.
Division of Oncology, Clinical Sciences, Lund University, Lund, Sweden.
Clin Epidemiol. 2025 Apr 17;17:409-419. doi: 10.2147/CLEP.S509873. eCollection 2025.
Statin use has been consistently associated with improved clinical outcomes (especially recurrence) in breast cancer in multiple observational studies backed by compelling preclinical evidence. The strength of this evidence warrants a clinical trial to test the efficacy of statin exposure on breast cancer recurrence.
The double-blind, phase III, randomized, placebo-controlled MASTER (MAmmary cancer STatins in ER positive breast cancer) trial includes women diagnosed with early-stage, estrogen receptor-positive (ER+) breast cancer who are candidates for systemic (neo)adjuvant therapy. Enrolled patients are given standard (neo)adjuvant therapy and additionally randomized to either atorvastatin (80 mg/day) or placebo for two years. The trial's primary outcome is invasive disease-free survival (IDFS), with a target accrual of 3360 patients in total to achieve 80% power (two-sided alpha=0.05) to detect a 25% reduction in the risk of an IDFS event comparing the statin and placebo arms. At 3-, 6-, 12-, and 24-month follow-up time points, patients will have blood drawn for biomarker studies, answer patient-reported outcome (PRO) questionnaires, and control for adverse events. Subsequently, patients will receive annual PRO-criteria for Adverse Events (CTCAE) questionnaires until the completion of their 10 years of follow-up. Secondary endpoints include additional clinical endpoints; pathological response (neo-adjuvant treated patients), recurrence-free survival, distant-recurrence-free interval, overall survival and cardiac death-free interval, co-morbidity, and health-related quality-of-life measured by PRO-CTCAE questionnaires during and beyond study medication. Translational endpoints are evaluated in collected blood- and tumor samples.
If a protective effect of statins on breast cancer recurrence is supported by evidence from the MASTER trial, then the indications for a safe, well-tolerated, and inexpensive treatment can be expanded towards improved clinical outcomes for breast cancer patients.
在多项有令人信服的临床前证据支持的观察性研究中,他汀类药物的使用一直与乳腺癌临床结局(尤其是复发)的改善相关。该证据的力度足以开展一项临床试验,以检验他汀类药物暴露对乳腺癌复发的疗效。
双盲、III期、随机、安慰剂对照的MASTER(雌激素受体阳性乳腺癌中的他汀类药物)试验纳入了被诊断为早期雌激素受体阳性(ER+)乳腺癌且适合进行全身(新)辅助治疗的女性。入组患者接受标准(新)辅助治疗,并额外随机分为阿托伐他汀组(80毫克/天)或安慰剂组,为期两年。该试验的主要结局是无侵袭性疾病生存期(IDFS),目标是总共招募3360名患者,以达到80%的检验效能(双侧α=0.05),以检测他汀类药物组与安慰剂组相比IDFS事件风险降低25%。在3个月、6个月、12个月和24个月的随访时间点,患者将接受血液采集以进行生物标志物研究,回答患者报告结局(PRO)问卷,并控制不良事件。随后,患者将每年接受不良事件PRO标准(CTCAE)问卷,直至完成10年随访。次要终点包括其他临床终点;病理反应(新辅助治疗患者)、无复发生存期、无远处复发生存期、总生存期和无心脏死亡生存期、合并症,以及在研究用药期间及之后通过PRO-CTCAE问卷测量的健康相关生活质量。在采集的血液和肿瘤样本中评估转化终点。
如果MASTER试验的证据支持他汀类药物对乳腺癌复发有保护作用,那么一种安全、耐受性良好且廉价治疗的适应证可扩大至改善乳腺癌患者的临床结局。