Henry N Lynn, Giles Jon T, Stearns Vered
Division of Hematology/Oncology, Department of Internal Medicine, University of Michigan, Medical School, Ann Arbor, Michigan 48109-5419, USA.
Oncology (Williston Park). 2008 Nov 15;22(12):1401-8.
The introduction of aromatase inhibitor (AI) therapy for the adjuvant treatment of postmenopausal women with hormone receptor-positive breast cancer has led to a significant change in the management of the disease. AIs are slightly more efficacious and initially appeared to have a better toxicity profile compared to the previous gold standard, tamoxifen. However, increased use of AIs in the community setting has led to the recognition that the clinical impact of the musculoskeletal side effects is substantial. This review will describe the variety of AI-associated musculoskeletal symptoms (AIMSS), potential mechanisms underlying the development of the toxicity, and available treatment options for these side effects. Increased knowledge about the etiology and management of this clinically important toxicity could potentially improve patient adherence to AI therapy, thereby leading to a reduction in breast cancer recurrence and death.
芳香化酶抑制剂(AI)疗法被引入用于激素受体阳性绝经后乳腺癌女性的辅助治疗,这给该疾病的管理带来了重大变革。与之前的金标准他莫昔芬相比,AI的疗效略高,且最初似乎具有更好的毒性特征。然而,在社区环境中AI使用的增加使得人们认识到肌肉骨骼副作用的临床影响相当大。本综述将描述各种与AI相关的肌肉骨骼症状(AIMSS)、毒性发生的潜在机制以及针对这些副作用的可用治疗选择。对这种具有临床重要性的毒性的病因和管理有更多了解,可能会提高患者对AI治疗的依从性,从而降低乳腺癌复发和死亡风险。