Department of Obstetrics and Gynecology, Erlangen University Hospital, Comprehensive Cancer Center Erlangen-European Metropolitan Area Nuremberg, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany.
Department of Gynecology, Heinrich Heine University of Düsseldorf, Düsseldorf, Germany; Department of Gynecology, University of Tübingen, Tübingen, Germany.
Eur J Cancer. 2018 Jun;96:82-90. doi: 10.1016/j.ejca.2018.03.020. Epub 2018 Apr 18.
Endocrine treatment (ET) with an aromatase inhibitor (AI) is the treatment of choice in post-menopausal patients with hormone receptor-positive early breast cancer (EBC). However, adverse events (AEs) often lead to treatment discontinuation. This analysis aimed to identify side-effects that lead to patients failing to persist with letrozole treatment.
Post-menopausal hormone receptor-positive EBC patients starting ET with letrozole were enroled in EvAluate-TM, a non-interventional study. Information regarding treatment compliance and persistence was gathered in months 6 and 12. Persistence was defined as the time from 30 d after the start to the end of treatment. The influence on persistence of musculoskeletal syndrome, menopausal disorder, sleep disorder and other AEs within the first 30 d was analysed using Cox regression analyses.
Among 3887 patients analysed, the persistence rate after 12 months was >85%. In all, 568 patients (14.6%) discontinued the treatment, 358 of whom (63.0%) did so only because of side-effects. The main AEs influencing persistence were musculoskeletal symptoms (hazard ratio [HR] 2.55; 95% confidence interval [CI], 1.90-3.42), sleep disorders (HR 1.95; 95% CI, 1.41-2.70) and other AEs (HR 2.03; 95% CI, 1.51-2.73). Menopausal disorder was not associated with non-persistence (HR 1.17; 95% CI, 0.74-1.84).
These results suggest that side-effects of AIs such as musculoskeletal syndrome and sleep disorder lead to ET discontinuation within the first treatment year in significant numbers of EBC patients. Compliance programmes adapted for subgroups that are at risk for early non-persistence might help to ensure the recommended therapy duration.
CFEM345DDE19.
芳香化酶抑制剂(AI)的内分泌治疗(ET)是激素受体阳性早期乳腺癌(EBC)绝经后患者的首选治疗方法。然而,不良事件(AE)常常导致治疗中断。本分析旨在确定导致患者无法坚持来曲唑治疗的副作用。
开始来曲唑 ET 的绝经后激素受体阳性 EBC 患者参加了非干预性研究 EvAluate-TM。在第 6 和 12 个月收集了关于治疗依从性和持久性的信息。持久性定义为从开始后的第 30 天到治疗结束的时间。使用 Cox 回归分析在第 30 天内分析了肌肉骨骼综合征、绝经障碍、睡眠障碍和其他 AE 对持久性的影响。
在分析的 3887 例患者中,12 个月后的持续率>85%。共有 568 例患者(14.6%)停止治疗,其中 358 例(63.0%)仅因副作用停药。影响持久性的主要 AE 是肌肉骨骼症状(风险比 [HR] 2.55;95%置信区间 [CI],1.90-3.42)、睡眠障碍(HR 1.95;95% CI,1.41-2.70)和其他 AE(HR 2.03;95% CI,1.51-2.73)。绝经障碍与非持续性无关(HR 1.17;95% CI,0.74-1.84)。
这些结果表明,AI 引起的肌肉骨骼综合征和睡眠障碍等副作用导致许多 EBC 患者在治疗的第一年中断 ET。为有早期非持续性风险的亚组制定适应性依从性计划可能有助于确保推荐的治疗持续时间。
CFEM345DDE19。