Endocrinology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Internal Medicine, Lahey Hospital and Medical Center, Burlington, MA, USA.
Br J Clin Pharmacol. 2019 Jun;85(6):1125-1135. doi: 10.1111/bcp.13834. Epub 2019 Jan 25.
Potent antiresorptive drugs (bisphosphonate and denosumab) are often used to protect bone health in postmenopausal breast cancer patients. In addition, clinical trials have shown that these drugs increase disease-free survival, though the mechanism of adjuvant benefit is largely unknown. Here we review the bone health and adjuvant data for both classes of antiresorptive drugs and highlight differences in their pharmacology. Inhibition of bone resorption is vitally important to protect against osteoporotic fractures, and may also contribute to adjuvant survival benefits by making the bone microenvironment less amenable to breast cancer metastasis. After a course of therapy, stoppage of bisphosphonates yields a persistent antiresorptive effect, whereas discontinuation of denosumab causes a rebound increase in bone resorption markers and a loss of bone mineral density to baseline levels. Whether the potential adjuvant benefits of denosumab are also rapidly lost after drug discontinuation deserves further investigation.
强效抗吸收药物(双膦酸盐和地舒单抗)常用于保护绝经后乳腺癌患者的骨骼健康。此外,临床试验表明这些药物可以提高无病生存率,尽管辅助治疗获益的机制尚不清楚。在这里,我们回顾了这两类抗吸收药物的骨骼健康和辅助数据,并强调了它们在药理学上的差异。抑制骨吸收对于预防骨质疏松性骨折至关重要,并且通过使骨骼微环境更不易发生乳腺癌转移,也可能有助于辅助生存获益。在一个疗程的治疗后,停止使用双膦酸盐会产生持续的抗吸收作用,而停止使用地舒单抗会导致骨吸收标志物的反弹增加,并使骨密度恢复到基线水平。地舒单抗的潜在辅助获益在停药后是否也迅速丧失,值得进一步研究。