Grigorian Nelly, Baumrucker Steven J
ETSU College of Medicine, Johnson City, TN, USA.
Palliative Medicine, Ballad Health System, Johnson City, TN, USA.
SAGE Open Med. 2022 Mar 19;10:20503121221078722. doi: 10.1177/20503121221078722. eCollection 2022.
Since their introduction into clinical use in the 1970s, aromatase inhibitors have been a cornerstone of therapy for estrogen-receptor positive breast cancer in postmenopausal women. Unfortunately, this therapy leads to estrogen depletion in the body, which can lead to unpleasant side effects such as menopausal symptoms like hot flashes, insomnia, slightly increased risk of ischemic heart disease, accelerated bone loss leading to higher osteoporosis risk, and most significantly, arthralgias. The joint pain induced by aromatase inhibitor therapy is frequently cited as the leading cause of premature discontinuation; approximately 50% of patients will report new onset or worsening joint pain 1 year after therapy initiation, approximately 30% of patients discontinue therapy after 1 year, and only 50%-68% of patients remain fully compliant with therapy after 3 years. This article will describe risk factors for aromatase inhibitor-associated musculoskeletal syndrome, including genetic predispositions correlated with an increased risk of this syndrome, explain the currently understood pathophysiology, and give an overview of effective treatment options in managing this syndrome.
自20世纪70年代引入临床应用以来,芳香化酶抑制剂一直是绝经后女性雌激素受体阳性乳腺癌治疗的基石。不幸的是,这种疗法会导致体内雌激素水平下降,进而引发一些令人不适的副作用,如潮热、失眠等更年期症状,缺血性心脏病风险略有增加,骨质流失加速导致骨质疏松风险升高,最显著的是关节疼痛。芳香化酶抑制剂治疗引起的关节疼痛常被认为是提前停药的主要原因;约50%的患者在治疗开始1年后会报告出现新的或加重的关节疼痛,约30%的患者在1年后停药,3年后仅有50%-68%的患者仍能完全依从治疗。本文将描述芳香化酶抑制剂相关肌肉骨骼综合征的风险因素,包括与该综合征风险增加相关的遗传易感性,解释目前所了解的病理生理学,并概述管理该综合征的有效治疗选择。