Johns Hopkins Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Hematology/Oncology Fellowship Program, Vanderbilt University Medical Center, Nashville, TN, USA.
J Cancer Surviv. 2024 Oct;18(5):1683-1696. doi: 10.1007/s11764-023-01408-y. Epub 2023 Jun 1.
Weight gain after breast cancer poses health risks. We aimed to identify factors associated with weight gain during adjuvant endocrine therapy (AET).
Women initiating AET enrolled in a prospective cohort. Participants completed FACT-ES plus PROMIS pain interference, depression, anxiety, fatigue, sleep disturbance and physical function measures at baseline, 3, 6, 12, 24, 36, 48 and 60 months. Treatment-emergent symptoms were defined as changes in scores in the direction indicative of worsening symptoms that exceeded the minimal important difference at 3 and/or 6 months compared to baseline. We used logistic regression to evaluate associations of clinicodemographic features and treatment-emergent symptoms with clinically significant weight gain over 60 months (defined as ≥ 5% compared to baseline) in pre- and post-menopausal participants.
Of 309 participants, 99 (32%) were pre-menopausal. The 60 months cumulative incidence of clinically significant weight gain was greater in pre- than post-menopausal participants (67% vs 43%, p < 0.001). Among pre-menopausal participants, treatment-emergent pain interference (OR 2.49), aromatase inhibitor receipt (OR 2.8), mastectomy, (OR 2.06) and White race (OR 7.13) were associated with weight gain. Among post-menopausal participants, treatment-emergent endocrine symptoms (OR 2.86), higher stage (OR 2.25) and White race (OR 2.29) were associated with weight gain while treatment-emergent physical function decline (OR 0.30) was associated with lower likelihood of weight gain.
Weight gain during AET is common, especially for pre-menopausal women. Clinicodemographic features and early treatment-emergent symptoms may identify at risk individuals.
Patients at risk for weight gain can be identified early during AET.
NCT01937052, registered September 3, 2013.
乳腺癌治疗后体重增加会带来健康风险。本研究旨在确定辅助内分泌治疗(AET)期间体重增加的相关因素。
参与前瞻性队列研究的女性在开始 AET 时入组。参与者在基线、3、6、12、24、36、48 和 60 个月时完成 FACT-ES 加 PROMIS 疼痛干扰、抑郁、焦虑、疲劳、睡眠障碍和身体功能测量。治疗后出现的症状定义为与基线相比,3 个月和/或 6 个月时,表明症状恶化且超过最小有意义差异的评分变化。我们使用逻辑回归评估临床和人口统计学特征以及治疗后出现的症状与绝经前和绝经后参与者 60 个月时(与基线相比≥5%)临床显著体重增加的相关性。
在 309 名参与者中,99 名(32%)为绝经前。与绝经后参与者相比,绝经前参与者 60 个月的临床显著体重增加累积发生率更高(67%比 43%,p<0.001)。在绝经前参与者中,治疗后出现的疼痛干扰(OR 2.49)、使用芳香化酶抑制剂(OR 2.8)、乳房切除术(OR 2.06)和白种人(OR 7.13)与体重增加相关。在绝经后参与者中,治疗后出现的内分泌症状(OR 2.86)、较高的分期(OR 2.25)和白种人(OR 2.29)与体重增加相关,而治疗后出现的身体功能下降(OR 0.30)与体重增加的可能性降低相关。
AET 期间体重增加很常见,尤其是绝经前女性。临床和人口统计学特征以及早期治疗后出现的症状可能可以识别出有风险的个体。
可以在 AET 期间早期识别出有体重增加风险的患者。
NCT01937052,于 2013 年 9 月 3 日注册。