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乳腺癌治疗过程中的体力活动、功能能力和心脏功能的变化。

Changes in Physical Activity, Functional Capacity, and Cardiac Function during Breast Cancer Therapy.

出版信息

Cancer Epidemiol Biomarkers Prev. 2022 Jul 1;31(7):1509. doi: 10.1158/1055-9965.EPI-22-0470.

Abstract

PURPOSE

Functional capacity and cardiac function can decline during breast cancer (BC) therapy. In non-cancer populations, higher physical activity (PA) is associated with better physical function and cardiac health. This study compared baseline PA, functional capacity, and cardiac function between women with and without BC and tested if greater PA participation was related to higher functional capacity and/or better heart function after three months of BC therapy.

METHODS

Data was collected in 104 women without BC (82% Caucasian, baseline only) and 110 women with stage I-III BC (82% Caucasian) before therapy and after three months of treatment. Participants self-reported PA and underwent six-minute walk distance (6MWD) testing to measure functional capacity and cardiovascular magnetic resonance to assess left ventricular ejection fraction (LVEF). Analyses were adjusted for age, race, body mass index (BMI), and medication use.

RESULTS

The BC group was older (56.2 ± 10.7 vs 52.1 ± 14.7 yrs, P=0.02) with a higher average BMI than the non-cancer group (30.3 ± 6.8 vs 27.7 ± 6.2 kg/m2, P<0.01). Pre-treatment, BC participants reported lower PA scores (27.9 ± 2.8 vs 34.9 ± 2.8, P=0.04) with similar 6MWD and LVEF relative to those without cancer (485 ± 11 vs 496 ± 11 m, P=0.4 and 59.7 ± 0.7 vs 58.9 ± 0.8%, P=0.37, respectively). After three months of BC therapy, declines were observed for PA scores (27.9 ± 2.8 vs 18.3 ± 2.5, P=0.02), 6MWD (485 ± 11 vs 428 ± 10 m, P<0.001), and LVEF (59.7 ± 0.7 vs 56.1 ± 0.7%, P<0.001). Compared to BC participants who reported no PA at three months (n=24, 22%), BC women who reported any PA (n=78, 86%) had higher 6MWD (442 ± 11 vs 389 ± 17 m, P=0.006) but similar LVEF (56.5 ± 0.9 vs 55.3 ± 1.5%, p=0.5). Women who reported any PA were less likely to exhibit an LVEF below normal (<50%) or decline in LVEF of 'â•10 points compared to inactive women (BMI-adjusted, OR [95% CI]: 0.27 [0.09, 0.85]).

CONCLUSIONS

These preliminary results indicate that self-reported PA, LVEF and 6MWD decline in the first three months of BC treatment, but PA participation during BC treatment may mitigate declines in functional capacity and cardiac function. Further research is needed to identify barriers and facilitators of PA participation during BC therapy.

FUNDING

Data collection was funded by the Wake Forest NCORP Research Base grant 2UG1CA189824 with support of the NCI Community Oncology Research Program (NCORP). Additional funding for this study was provided by grants from the National Institutes of Health, National Cancer Institute (1R01CA199167 and 5T32CA093423).

CLINICAL TRIAL ID

NCT02791581 for WF97415 UPBEAT.

摘要

目的

在乳腺癌(BC)治疗过程中,功能能力和心脏功能可能会下降。在非癌症人群中,较高的体力活动(PA)与更好的身体功能和心脏健康相关。本研究比较了患有和不患有 BC 的女性之间的基线 PA、功能能力和心脏功能,并测试了在 BC 治疗三个月后,更多的 PA 参与是否与更高的功能能力和/或更好的心脏功能相关。

方法

在治疗前和治疗后三个月,收集了 104 名无 BC 的女性(82%为白种人,仅基线数据)和 110 名患有 I-III 期 BC 的女性(82%为白种人)的数据。参与者自我报告 PA,并进行了六分钟步行距离(6MWD)测试,以测量功能能力和心血管磁共振评估左心室射血分数(LVEF)。分析调整了年龄、种族、体重指数(BMI)和药物使用。

结果

BC 组年龄较大(56.2 ± 10.7 岁比 52.1 ± 14.7 岁,P=0.02),平均 BMI 高于非癌症组(30.3 ± 6.8 千克/平方米比 27.7 ± 6.2 千克/平方米,P<0.01)。治疗前,BC 参与者报告的 PA 得分较低(27.9 ± 2.8 比 34.9 ± 2.8,P=0.04),6MWD 和 LVEF 与无癌症的患者相似(485 ± 11 比 496 ± 11 米,P=0.4 和 59.7 ± 0.7 比 58.9 ± 0.8%,P=0.37,分别)。在 BC 治疗三个月后,PA 评分(27.9 ± 2.8 比 18.3 ± 2.5,P=0.02)、6MWD(485 ± 11 比 428 ± 10 米,P<0.001)和 LVEF(59.7 ± 0.7 比 56.1 ± 0.7%,P<0.001)均下降。与报告三个月内无 PA 的 BC 参与者(n=24,22%)相比,报告有任何 PA 的 BC 女性(n=78,86%)的 6MWD 更高(442 ± 11 比 389 ± 17 米,P=0.006),但 LVEF 相似(56.5 ± 0.9 比 55.3 ± 1.5%,P=0.5)。与不活动的女性相比,报告有任何 PA 的女性出现 LVEF 低于正常(<50%)或 LVEF 下降 â•10 分的可能性较小(BMI 调整后,OR [95%CI]:0.27 [0.09, 0.85])。

结论

这些初步结果表明,在 BC 治疗的头三个月中,自我报告的 PA、LVEF 和 6MWD 下降,但在 BC 治疗期间参与 PA 可能会减轻功能能力和心脏功能的下降。需要进一步研究以确定 BC 治疗期间 PA 参与的障碍和促进因素。

资金

数据收集由 Wake Forest NCORP 研究基地赠款 2UG1CA189824 资助,得到 NCI 社区肿瘤学研究计划(NCORP)的支持。这项研究的额外资金来自美国国立卫生研究院、国立癌症研究所(1R01CA199167 和 5T32CA093423)的赠款。

临床试验注册号

NCT02791581(WF97415 UPBEAT)。

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