Statin Therapy in Early Breast Cancer: The MASTER Trial; A Randomized Phase III, Placebo-Controlled Comparison of Standard (Neo)Adjuvant Therapy Plus Atorvastatin versus Standard (Neo)Adjuvant Therapy Plus Placebo.

IF 3.4 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Clinical Epidemiology Pub Date : 2025-04-17 eCollection Date: 2025-01-01 DOI:10.2147/CLEP.S509873
Signe Borgquist, Maj-Britt Jensen, Cecilie Linea Bendorff, Peer Christiansen, Birgitte Vrou Offersen, Annette Raskov Kodahl, Marianne Ewertz, Anders Bonde Jensen, Thomas P Ahern, Deirdre Cronin-Fenton, Bent Ejlertsen
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引用次数: 0

Abstract

Purpose: 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.

Patients and methods: 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.

Discussion: 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.

他汀类药物治疗早期乳腺癌:MASTER试验标准(Neo)辅助治疗加阿托伐他汀与标准(Neo)辅助治疗加安慰剂的随机III期安慰剂对照比较
目的:在多项观察性研究中,他汀类药物的使用一直与乳腺癌临床结果的改善(尤其是复发)相关,这些研究有令人信服的临床前证据支持。这一证据的强度值得进行临床试验,以测试他汀类药物对乳腺癌复发的疗效。患者和方法:双盲,III期,随机,安慰剂对照MASTER(乳腺癌他汀类药物治疗ER阳性乳腺癌)试验包括诊断为早期,雌激素受体阳性(ER+)乳腺癌的女性,她们是全身(neo)辅助治疗的候选人。入组患者接受标准(新)辅助治疗,另外随机接受阿托伐他汀(80 mg/天)或安慰剂治疗,为期两年。该试验的主要终点是侵袭性无病生存期(IDFS),与他汀类药物组和安慰剂组相比,总共有3360例患者的目标累计达到80%的功率(双侧α =0.05),以检测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,患者将抽血进行生物标志物研究,回答患者报告的结果(PRO)问卷,并控制不良事件。随后,患者将接受年度不良事件PRO-criteria (CTCAE)问卷调查,直到完成10年的随访。次要终点包括额外的临床终点;病理反应(新辅助治疗患者)、无复发生存期、远端无复发间期、总生存期和心源性无死亡间期、合并症和与健康相关的生活质量,通过PRO-CTCAE问卷在研究用药期间和之后测量。在收集的血液和肿瘤样本中评估翻译终点。讨论:如果MASTER试验的证据支持他汀类药物对乳腺癌复发的保护作用,那么这种安全、耐受性良好且价格低廉的治疗方法的适应症可以扩大,以改善乳腺癌患者的临床结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Epidemiology
Clinical Epidemiology Medicine-Epidemiology
CiteScore
6.30
自引率
5.10%
发文量
169
审稿时长
16 weeks
期刊介绍: Clinical Epidemiology is an international, peer reviewed, open access journal. Clinical Epidemiology focuses on the application of epidemiological principles and questions relating to patients and clinical care in terms of prevention, diagnosis, prognosis, and treatment. Clinical Epidemiology welcomes papers covering these topics in form of original research and systematic reviews. Clinical Epidemiology has a special interest in international electronic medical patient records and other routine health care data, especially as applied to safety of medical interventions, clinical utility of diagnostic procedures, understanding short- and long-term clinical course of diseases, clinical epidemiological and biostatistical methods, and systematic reviews. When considering submission of a paper utilizing publicly-available data, authors should ensure that such studies add significantly to the body of knowledge and that they use appropriate validated methods for identifying health outcomes. The journal has launched special series describing existing data sources for clinical epidemiology, international health care systems and validation studies of algorithms based on databases and registries.
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