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

描述(申请人提供)：在美国诊断的所有乳腺癌中，三分之二的女性表达雌激素和/或黄体酮受体。尽管他莫昔芬5年来一直是激素受体阳性的早期乳腺癌妇女的标准激素辅助疗法，但芳香酶抑制剂(AI)已迅速取代他莫昔芬成为激素疗法的选择。几项大型辅助试验表明，与使用5年的他莫昔芬治疗相比，在他莫昔芬的替代或之后使用人工智能可以降低乳腺癌复发的风险。最近，美国临床肿瘤学会专家共识小组建议，所有患有早期激素受体阳性乳腺癌的绝经后女性都应接受人工智能，作为辅助治疗的一部分。然而，关于人工授精的安全性和毒性的长期数据在很大程度上是缺乏的。来自评估人工智能使用情况的大型辅助试验的数据表明，关节痛是与人工智能治疗相关的主要毒性反应之一，也是停止人工智能治疗的最常见原因之一。关于关节痛的有效治疗方法的数据很少。除了关节痛，人工智能治疗的其他与骨相关的不良反应包括骨丢失和骨折。虽然像双磷酸盐这样的药物可以用来缓解骨丢失，但这些药物也会产生明显的副作用。鉴于人工智能的有效性，至关重要的是探索更好的方法来管理这些制剂的毒性。管理人工智能副作用的非药物方法尤其可取。运动已被证明可以改善健康女性的骨代谢，对患有纤维肌痛、骨关节炎和类风湿性关节炎的人也有好处；然而，还没有随机试验研究运动对服用AIS的乳腺癌幸存者的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锻炼计划的能力，以减轻人工智能治疗的副作用。我们的试验将把180名绝经后乳腺癌患者随机分成一组，他们接受人工智能治疗至少6个月，目前至少经历着在开始人工智能治疗后开始的轻微关节痛，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疼痛严重程度的影响，运动对关节疼痛效果的中介因素，以及人工智能治疗的其他副作用，包括内分泌相关的生活质量和骨密度。女性将被随机分到以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。被随机安排参加锻炼的女性将参加150分钟/周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个月的临床访问，以及3个月和9个月的邮寄，以评估干预对研究结果的影响。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人工智能相关的副作用，并减少过早停止使用这些药物的女性数量，我们相信我们的研究可能会证明对每年被诊断为激素受体阳性乳腺癌的大量绝经后女性是有益的。我们的研究还将与NCI和癌症生存办公室的使命特别相关，该使命旨在改善癌症幸存者的生活质量，支持介入生存研究，并确保满足幸存者健康需求的最佳实践。公共卫生相关性：美国临床肿瘤学会最近的一个专家共识小组建议，所有患有早期激素受体阳性乳腺癌的绝经后妇女(约占所有确诊乳腺癌妇女的三分之二)接受芳香酶抑制剂(AI)作为辅助治疗的一部分。来自评估人工智能使用情况的大型辅助试验的数据表明，关节疼痛和骨丢失是人工智能治疗的主要毒性反应，也是停止人工智能治疗的最常见原因。我们的试验将检验锻炼计划在缓解人工智能相关副作用方面的影响，如关节疼痛、骨密度和内分泌相关的生活质量，并可能被证明对每年被诊断为激素受体阳性乳腺癌的大量绝经后女性有益。

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.