Health-related quality of life and physical activity collected via mobile application and wearable device in patients with HR +/HER2 - advanced breast cancer treated with palbociclib plus endocrine therapy or endocrine therapy alone: 6-month longitudinal study (JBCRG-26).

IF 2.9
Hiroko Bando, Aya Ueda, Kaori Terata, Mihoko Doi, Shigenori E Nagai, Masaya Hattori, Kenichi Watanabe, Nobuko Tamura, Manabu Futamura, Kei Koizumi, Naoki Niikura, Tempei Miyaji, Yasuaki Muramatsu, Linghua Xu, Norikazu Masuda, Shigehira Saji
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Abstract

Objectives: To summarize descriptively health-related quality of life (HRQOL) and physical activity (PA) evaluated with a mobile application and wearable device among patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR + /HER2 -) advanced breast cancer (ABC) treated with first- or second-line palbociclib plus endocrine therapy (ET) or ET alone.

Methods: HRQOL was assessed with the EORTC QLQ-C30 at baseline and Day 15 of 6 treatment cycles (~ 24 weeks). PA metrics were averaged on a weekly basis for 24 weeks. Co-primary endpoints were mean change from baseline in Global Health Status (GHS) and sedentary time.

Results: Ninety-nine patients were enrolled; 78 received palbociclib plus ET (mean age: 57.2 years; 75.6% initiated first-line treatment) and 21 received ET alone (mean age: 56.3 years; 90.5% initiated first-line treatment). Baseline mean GHS score was 60.9 in the palbociclib plus ET group and 64.3 in the ET alone group; mean changes from baseline to Day 15 of Cycle 6 were +4.8 and +2.9, respectively, and not deteriorated beyond the 10-point clinically significant threshold in either treatment group. Baseline mean sedentary time was 581 min/day in the palbociclib plus ET group and 513 min/day in the ET alone group; mean changes from baseline to Week 24 were -22 and -102 min/day, respectively.

Conclusions: In this real-world study of women with HR+/HER2- ABC in Japan, neither palbociclib plus ET nor ET alone had any substantial detrimental impacts on HRQOL, according to patients' assessments recorded in a smartphone-based mobile application, and PA, as measured by a wearable device.

Trial registration: ClinicalTrials.gov NCT04736576; registered, February 3, 2021.

通过移动应用程序和可穿戴设备收集HR +/HER2 -晚期乳腺癌患者接受帕博西尼联合内分泌治疗或单独内分泌治疗的健康相关生活质量和身体活动:6个月的纵向研究(JBCRG-26)。
目的:总结使用移动应用程序和可穿戴设备评估激素受体阳性/人表皮生长因子受体2阴性(HR + /HER2 -)晚期乳腺癌(ABC)患者的描述性健康相关生活质量(HRQOL)和身体活动(PA),这些患者接受一线或二线帕博西尼加内分泌治疗(ET)或单独ET治疗。方法:在基线和6个治疗周期(~ 24周)的第15天采用EORTC QLQ-C30评估HRQOL。PA指标在24周内每周平均一次。共同主要终点是全球健康状况(GHS)与基线的平均变化和久坐时间。结果:99例患者入组;78人接受帕博西尼加ET治疗(平均年龄:57.2岁;75.6%开始一线治疗),21人单独接受ET治疗(平均年龄:56.3岁;90.5%开始了一线治疗)。帕博西尼加ET组基线平均GHS评分为60.9,单独ET组为64.3;从基线到第6周期第15天的平均变化分别为+4.8和+2.9,两组均未恶化超过10点的临床显著阈值。帕博西尼加ET组的基线平均久坐时间为581分钟/天,单独ET组为513分钟/天;从基线到第24周的平均变化分别为-22分钟/天和-102分钟/天。结论:在日本对HR+/HER2- ABC女性的现实世界研究中,根据基于智能手机的移动应用程序记录的患者评估和可穿戴设备测量的PA,帕博西尼加ET或单独ET对HRQOL都没有任何实质性的有害影响。试验注册:ClinicalTrials.gov NCT04736576;注册日期:2021年2月3日。
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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