RCT of exercise on aromatase inhibitor side effects in breast cancer survivors

描述（由申请人提供）：在美国女性中诊断的所有乳腺癌中有三分之二表达雌激素和/或孕激素受体。尽管5年的他莫昔芬长期以来一直是患有早期激素受体阳性乳腺癌的女性的标准辅助激素治疗，但芳香酶抑制剂（AI）已迅速取代他莫昔芬作为激素治疗的选择。几项大型辅助试验表明，与5年的他莫昔芬治疗相比，使用AI代替他莫昔芬或在他莫昔芬之后使用AI降低了乳腺癌复发的风险。最近美国临床肿瘤学会专家共识小组建议所有绝经后早期乳腺癌患者接受AI作为辅助治疗的一部分。然而，关于AI的安全性和毒性的长期数据在很大程度上缺乏。来自评估AI使用的大型辅助试验的数据表明，关节痛是与AI治疗相关的主要毒性之一，也是AI治疗中止的最常见原因之一。关于有效治疗关节痛的数据很少。除了关节痛，AI治疗的其他与骨骼相关的不良反应包括骨质流失和骨折。虽然双膦酸盐等药物可用于缓解骨质流失，但这些药物也会引起显著的副作用。鉴于人工智能的功效，探索更好的方法来管理这些药剂的毒性是至关重要的。管理AI副作用的非药物方法是特别可取的。运动已被证明可以改善健康女性的骨代谢，并对纤维肌痛，骨关节炎和类风湿性关节炎患者有益;然而，没有随机试验研究运动对服用AI的乳腺癌幸存者关节痛或骨量的影响。在拟议的试验中，我们计划评估步行和力量训练运动计划减轻AI治疗副作用的能力。我们的试验将随机选择180名绝经后乳腺癌患者，他们已经服用AI至少6个月，并且目前正在经历至少轻度关节痛，这些关节痛是在开始AI治疗后开始的，他们将接受为期一年的运动干预或注意力控制组。然后，我们将研究运动对关节痛严重程度的影响，调节运动对关节痛影响的因素，以及AI治疗的其他副作用，包括内分泌相关的生活质量和骨矿物质密度。妇女将被随机分配到家庭和健身房为基础的锻炼计划或注意力控制（健康教育）组。随机分配到运动组的女性将参加每周150分钟的有氧运动和每周两次的力量训练计划。我们将进行基线、6个月和12个月的门诊访视，以及3个月和9个月的邮寄，以评估干预对研究结局的影响。鉴于人工智能的广泛使用，我们相信我们的方法是创新和及时的。如果我们的干预能够减轻AI相关的副作用，并减少过早停药的女性数量，我们相信我们的研究可能会对每年诊断为激素受体阳性乳腺癌的大量绝经后女性有益。我们的研究也将特别与NCI和癌症幸存者办公室的使命相关，以提高癌症幸存者的生活质量，支持干预生存研究，并确保解决幸存者健康需求的最佳实践。公共卫生相关性：最近美国临床肿瘤学会专家共识小组建议，所有绝经后早期乳腺癌患者（约2/3诊断为乳腺癌的女性）接受芳香化酶抑制剂（AI）作为辅助治疗的一部分。来自评估AI使用的大型辅助试验的数据表明，关节痛和骨丢失是与AI治疗相关的主要毒性，也是AI治疗中止的最常见原因。我们的试验将检查运动计划对减轻AI相关副作用的影响，如关节痛，骨密度和内分泌相关的生活质量，并可能证明对每年诊断为激素受体阳性乳腺癌的大量绝经后妇女有益。

DESCRIPTION (provided by applicant): Two thirds of all breast cancers diagnosed in US women express estrogen and/or progesterone receptors. Although 5 years of tamoxifen had long been the standard adjuvant hormonal therapy for women with early- stage, hormone receptor-positive breast cancer, the aromatase inhibitors (AI's) have rapidly supplanted tamoxifen as the hormonal therapy of choice. Several large adjuvant trials have demonstrated that using an AI in place of or after tamoxifen reduced the risk of breast cancer recurrence, as compared to treatment with 5 years of tamoxifen. A recent American Society of Clinical Oncology expert consensus panel recommended that all postmenopausal women with early-stage, hormone-receptor-positive breast cancer receive an AI as part of their adjuvant therapy. However, long term data regarding the safety and toxicity of AIs is largely lacking. Data from the large adjuvant trials evaluating the use of the AI's indicate that arthralgia is one of the major toxicities associated with AI therapy and one of the most common reasons for AI treatment discontinuation. There has been little data regarding effective treatments for arthralgias. In addition to arthralgia, other bone-related adverse effects of AI therapy include bone loss and fractures. Although medications such as bisphosphonates can be used to alleviate bone loss, these drugs also cause significant side effects. Given the efficacy of the AI's, it is essential that better ways to manage the toxicity of these agents be explored. Nonpharmacologic methods of managing the side effects of the AI's are especially desirable. Exercise has been shown to improve bone metabolism in healthy women, and to be beneficial for people with fibromyalgia, osteoarthritis and rheumatoid arthritis; however, no randomized trial has examined the impact of exercise on arthralgia or bone mass in breast cancer survivors taking AIs. In the proposed trial, we plan to evaluate the ability of a walking and strength training exercise program to attenuate side effects of AI therapy. Our trial will randomize 180 postmenopausal breast cancer patients, who have been taking an AI for at least 6 months and are currently experiencing at least mild arthralgia which started after initiating AI therapy, to a yearlong exercise intervention or to an attention control group. We will then examine the impact of exercise on severity of arthralgia, factors mediating the effect of exercise on arthralgia, and other side effects of AI therapy including endocrine-related quality of life and bone mineral density. Women will be randomized to a home- and gym-based exercise program or attention control (health education) group. Women randomized to exercise will participate in 150 min/wk of aerobic exercise and a twice-weekly strength training program. We will conduct baseline, 6- and 12-month clinic visits, as well as 3- and 9-month mailings to evaluate the effect of the intervention on study outcomes. Given the widespread use of the AI's, we believe that our approach is innovative and timely. If our intervention is able to alleviate AI-associated side effects and reduce the number of women who prematurely discontinue them, we believe that our study may prove beneficial for the large number of postmenopausal women diagnosed with hormone receptor-positive breast cancer each year. Our study will also be especially relevant to the mission of NCI and the Office of Cancer Survivorship to improve the quality of life for cancer survivors, support intervention survivorship research, and to ensure best practices for addressing the health needs of survivors. PUBLIC HEALTH RELEVANCE: A recent American Society of Clinical Oncology expert consensus panel recommended that all postmenopausal women with early-stage, hormone-receptor-positive breast cancer (~2/3 of all women diagnosed with breast cancer) receive an aromatase-inhibitor (AI) as part of their adjuvant therapy. Data from the large adjuvant trials evaluating the use of the AI's indicate that arthralgia and bone loss are the major toxicities associated with AI therapy and the most common reasons for AI treatment discontinuation. Our trial will examine the impact of an exercise program on alleviating AI-associated side effects such as arthralgia, bone mineral density, and endocrine-related quality of life, and may prove beneficial for the large number of postmenopausal women diagnosed with hormone receptor-positive breast cancer each year.