Pegington Mary, Zhen Tam Hui, Brentnall Adam, Sestak Ivana, Adams Judith, Blake Glen M, Gareth Evans D, Howell Anthony, Cuzick Jack, Harvie Michelle
The Prevent Breast Cancer Research Unit, The Nightingale Centre, Manchester University NHS Foundation Trust, Manchester, UK.
Division of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Wilmslow Road, Manchester M20 4BX, UK.
Prev Med Rep. 2024 Jan 22;38:102620. doi: 10.1016/j.pmedr.2024.102620. eCollection 2024 Feb.
Uptake to anastrozole for breast cancer prevention is low, partly due to women's concerns about side effects including gains in weight and specifically gains in body fat. Previous evidence does not link anastrozole with gains in weight, but there is a lack of data on any effects on body composition i.e. changes in fat and fat free mass. Here we assess association of anastrozole with body composition changes in a prospective sub-study from the second international breast intervention trial (IBIS-II).
Participants had DXA scans at baseline and for five years of anastrozole/placebo and beyond (between March 2004 and September 2017. Primary outcomes were changes in body weight, body fat and fat free mass at 9-18 months. A linear model was used to estimate the size of a differential effect in these outcomes by randomised treatment allocation adjusted for baseline value and time since last scan, age, 10-year breast cancer risk, smoking and HRT status.
203 postmenopausal women were recruited (n = 95 anastrozole, n = 108 placebo), mean age 58 years (SD = 5.4), BMI 28.0 kg/m (SD = 5.5). There was no evidence of a strong association between anastrozole or placebo and endpoints at 9-18 months; effect size (95 %CI) for anastrozole minus placebo for body weight (per/kg) -0.11 (-1.29-1.08); body fat 0.11 (-0.75-0.96) and fat free mass -0.30 (-0.79-0.19).
There is unlikely to be a clinically significant change to body composition with anastrozole for breast cancer prevention.
用于预防乳腺癌的阿那曲唑的使用率较低,部分原因是女性担心其副作用,包括体重增加,尤其是体脂增加。先前的证据并未将阿那曲唑与体重增加联系起来,但缺乏关于其对身体成分(即脂肪和去脂体重变化)影响的数据。在此,我们在第二项国际乳腺干预试验(IBIS-II)的一项前瞻性子研究中评估阿那曲唑与身体成分变化之间的关联。
参与者在基线时以及服用阿那曲唑/安慰剂五年及以后(2004年3月至2017年9月)进行了双能X线吸收测定(DXA)扫描。主要结局是9至18个月时体重、体脂和去脂体重的变化。采用线性模型,通过随机治疗分配估计这些结局的差异效应大小,并对基线值、自上次扫描以来的时间、年龄、10年乳腺癌风险、吸烟和激素替代疗法(HRT)状态进行校正。
招募了203名绝经后女性(阿那曲唑组n = 95,安慰剂组n = 108),平均年龄58岁(标准差= 5.4),体重指数(BMI)为28.0 kg/m²(标准差= 5.5)。没有证据表明阿那曲唑或安慰剂与9至18个月时的终点之间存在强关联;阿那曲唑减去安慰剂的效应大小(95%置信区间),体重(每千克)为-0.11(-1.29至1.08);体脂为0.11(-0.75至0.96),去脂体重为-0.30(-0.79至0.19)。
用于预防乳腺癌的阿那曲唑不太可能对身体成分产生具有临床意义的变化。