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辅助治疗后乳腺癌女性的体育活动

Physical activity for women with breast cancer after adjuvant therapy.

作者信息

Lahart Ian M, Metsios George S, Nevill Alan M, Carmichael Amtul R

机构信息

Faculty of Education, Health and Wellbeing, University of Wolverhampton, Gorway Road, Walsall, West Midlands, UK, WS1 3BD.

出版信息

Cochrane Database Syst Rev. 2018 Jan 29;1(1):CD011292. doi: 10.1002/14651858.CD011292.pub2.

Abstract

BACKGROUND

Women with a diagnosis of breast cancer may experience short- and long-term disease and treatment-related adverse physiological and psychosocial outcomes. These outcomes can negatively impact prognosis, health-related quality of life (HRQoL), and psychosocial and physical function. Physical activity may help to improve prognosis and may alleviate the adverse effects of adjuvant therapy.

OBJECTIVES

To assess effects of physical activity interventions after adjuvant therapy for women with breast cancer.

SEARCH METHODS

We searched the Cochrane Breast Cancer Group (CBCG) Specialised Registry, the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, Embase, the Cumulative Index to Nursing and Allied Health Literature (CINAHL), the Physiotherapy Evidence Database (PEDro), SPORTDiscus, PsycINFO, ClinicalTrials.gov, and the World Health Organization (WHO) International Clinical Trials Registry Platform, on 18 September 2015. We also searched OpenGrey and Healthcare Management Information Consortium databases.

SELECTION CRITERIA

We searched for randomised and quasi-randomised trials comparing physical activity interventions versus control (e.g. usual or standard care, no physical activity, no exercise, attention control, placebo) after adjuvant therapy (i.e. after completion of chemotherapy and/or radiation therapy, but not hormone therapy) in women with breast cancer.

DATA COLLECTION AND ANALYSIS

Two review authors independently selected studies, assessed risk of bias, and extracted data. We contacted trial authors to ask for additional information when needed. We calculated an overall effect size with 95% confidence intervals (CIs) for each outcome and used GRADE to assess the quality of evidence for the most important outcomes.

MAIN RESULTS

We included 63 trials that randomised 5761 women to a physical activity intervention (n = 3239) or to a control (n = 2524). The duration of interventions ranged from 4 to 24 months, with most lasting 8 or 12 weeks (37 studies). Twenty-eight studies included aerobic exercise only, 21 involved aerobic exercise and resistance training, and seven used resistance training only. Thirty studies described the comparison group as usual or standard care, no intervention, or control. One-fifth of studies reported at least 20% intervention attrition and the average physical activity adherence was approximately 77%.No data were available on effects of physical activity on breast cancer-related and all-cause mortality, or on breast cancer recurrence. Analysis of immediately postintervention follow-up values and change from baseline to end of intervention scores revealed that physical activity interventions resulted in significant small-to-moderate improvements in HRQoL (standardised mean difference (SMD) 0.39, 95% CI 0.21 to 0.57, 22 studies, 1996 women; SMD 0.78, 95% CI 0.39 to 1.17, 14 studies, 1459 women, respectively; low-quality evidence), emotional function (SMD 0.21, 95% CI 0.10 to 0.32, 26 studies, 2102 women, moderate-quality evidence; SMD 0.31, 95% CI 0.09 to 0.53, 15 studies, 1579 women, respectively; low-quality evidence), perceived physical function (SMD 0.33, 95% CI 0.18 to 0.49, 25 studies, 2129 women; SMD 0.60, 95% CI 0.23 to 0.97, 13 studies, 1433 women, respectively; moderate-quality evidence), anxiety (SMD -0.57, 95% CI -0.95 to -0.19, 7 studies, 326 women; SMD -0.37, 95% CI -0.63 to -0.12, 4 studies, 235 women, respectively; low-quality evidence), and cardiorespiratory fitness (SMD 0.44, 95% CI 0.30 to 0.58, 23 studies, 1265 women, moderate-quality evidence; SMD 0.83, 95% CI 0.40 to 1.27, 9 studies, 863 women, respectively; very low-quality evidence).Investigators reported few minor adverse events.Small improvements in physical activity interventions were sustained for three months or longer postintervention in fatigue (SMD -0.43, 95% CI -0.60 to -0.26; SMD -0.47, 95% CI -0.84 to -0.11, respectively), cardiorespiratory fitness (SMD 0.36, 95% CI 0.03 to 0.69; SMD 0.42, 95% CI 0.05 to 0.79, respectively), and self-reported physical activity (SMD 0.44, 95% CI 0.17 to 0.72; SMD 0.51, 95% CI 0.08 to 0.93, respectively) for both follow-up values and change from baseline scores.However, evidence of heterogeneity across trials was due to variation in intervention components (i.e. mode, frequency, intensity, duration of intervention and sessions) and measures used to assess outcomes. All trials reviewed were at high risk of performance bias, and most were also at high risk of detection, attrition, and selection bias. In light of the aforementioned issues, we determined that the evidence was of very low, low, or moderate quality.

AUTHORS' CONCLUSIONS: No conclusions regarding breast cancer-related and all-cause mortality or breast cancer recurrence were possible. However, physical activity interventions may have small-to-moderate beneficial effects on HRQoL, and on emotional or perceived physical and social function, anxiety, cardiorespiratory fitness, and self-reported and objectively measured physical activity. The positive results reported in the current review must be interpreted cautiously owing to very low-to-moderate quality of evidence, heterogeneity of interventions and outcome measures, imprecision of some estimates, and risk of bias in many trials. Future studies with low risk of bias are required to determine the optimal combination of physical activity modes, frequencies, intensities, and durations needed to improve specific outcomes among women who have undergone adjuvant therapy.

摘要

背景

被诊断患有乳腺癌的女性可能会经历短期和长期与疾病及治疗相关的不良生理和心理社会后果。这些后果会对预后、健康相关生活质量(HRQoL)以及心理社会和身体功能产生负面影响。体育活动可能有助于改善预后,并可能减轻辅助治疗的不良反应。

目的

评估辅助治疗后体育活动干预对乳腺癌女性患者的影响。

检索方法

我们于2015年9月18日检索了Cochrane乳腺癌协作组(CBCG)专业注册库、Cochrane对照试验中心注册库(CENTRAL)、MEDLINE、Embase、护理及相关健康文献累积索引(CINAHL)、物理治疗证据数据库(PEDro)、SPORTDiscus、PsycINFO、ClinicalTrials.gov以及世界卫生组织(WHO)国际临床试验注册平台。我们还检索了OpenGrey和医疗保健管理信息联盟数据库。

入选标准

我们检索了比较辅助治疗(即化疗和/或放疗完成后,但不包括激素治疗)后体育活动干预与对照(如常规或标准护理、无体育活动、无运动、注意力控制、安慰剂)的随机和半随机试验,研究对象为乳腺癌女性患者。

数据收集与分析

两位综述作者独立选择研究、评估偏倚风险并提取数据。必要时,我们联系试验作者以获取更多信息。我们计算了每个结局的总体效应量及95%置信区间(CI),并使用GRADE评估最重要结局的证据质量。

主要结果

我们纳入了63项试验,共5761名女性被随机分为体育活动干预组(n = 3239)或对照组(n = 2524)。干预持续时间为4至24个月,大多数持续8周或12周(37项研究)。28项研究仅包括有氧运动,21项涉及有氧运动和抗阻训练,7项仅使用抗阻训练。30项研究将比较组描述为常规或标准护理、无干预或对照。五分之一的研究报告至少20%的干预对象退出,平均体育活动依从性约为77%。目前尚无体育活动对乳腺癌相关死亡率、全因死亡率或乳腺癌复发影响的数据。对干预后立即随访值以及从基线到干预结束得分变化的分析表明,体育活动干预导致HRQoL有显著的小到中度改善(标准化均数差(SMD)0.39,95%CI 0.21至0.57,22项研究,1996名女性;SMD 0.78,95%CI 0.39至1.17,14项研究,1459名女性,低质量证据)、情绪功能(SMD 0.21,95%CI 0.10至0.32,26项研究,2102名女性,中等质量证据;SMD 0.31,95%CI 0.09至0.53,15项研究,1579名女性,低质量证据)、感知身体功能(SMD 0.33,95%CI 0.18至0.49,25项研究,2129名女性;SMD 0.60,95%CI 0.23至0.97,13项研究,1433名女性,中等质量证据)、焦虑(SMD -0.57,95%CI -0.95至-0.19,7项研究,326名女性;SMD -0.37,95%CI -0.63至-0.12,4项研究,235名女性,低质量证据)以及心肺适能(SMD 0.44,95%CI 0.30至0.58,23项研究,1265名女性,中等质量证据;SMD 0.83,95%CI 0.40至1.27,9项研究,863名女性,极低质量证据)。研究者报告的轻微不良事件较少。体育活动干预的小幅度改善在干预后三个月或更长时间内持续存在于疲劳(SMD -0.43,95%CI -0.60至-0.26;SMD -0.47,95%CI -0.84至-0.11,分别)、心肺适能(SMD 0.36,95%CI 0.03至0.69;SMD 0.42,95%CI 0.05至0.79,分别)以及自我报告的体育活动(SMD 0.44,95%CI 0.17至0.72;SMD 0.51,95%CI 0.08至0.93,分别)的随访值和从基线得分变化方面。然而,各试验间的异质性证据是由于干预成分(即干预和疗程的方式、频率、强度、持续时间)以及用于评估结局的测量方法的差异所致。所有纳入综述的试验均存在较高的实施偏倚风险,且大多数试验还存在较高的检测、失访和选择偏倚风险。鉴于上述问题,我们确定证据质量非常低、低或中等。

作者结论

关于乳腺癌相关死亡率、全因死亡率或乳腺癌复发无法得出结论。然而,体育活动干预可能对HRQoL、情绪或感知的身体和社会功能、焦虑、心肺适能以及自我报告和客观测量的体育活动有小到中度的有益影响。鉴于证据质量非常低到中等、干预和结局测量的异质性、一些估计的不精确性以及许多试验中的偏倚风险,本综述报告的阳性结果必须谨慎解读。未来需要开展偏倚风险低的研究,以确定改善辅助治疗后女性特定结局所需的体育活动方式、频率、强度和持续时间的最佳组合。

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