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Calcif Tissue Int. 2018 Jul;103(1):50-54. doi: 10.1007/s00223-018-0394-4. Epub 2018 Jan 29.
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The anti-tumor effect of RANKL inhibition in malignant solid tumors - A systematic review.RANKL 抑制在恶性实体瘤中的抗肿瘤作用 - 系统评价。
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The IUPHAR/BPS Guide to PHARMACOLOGY in 2018: updates and expansion to encompass the new guide to IMMUNOPHARMACOLOGY.2018 年 IUPHAR/BPS 药理学指南:更新和扩展,以包含新的免疫药理学指南。
Nucleic Acids Res. 2018 Jan 4;46(D1):D1091-D1106. doi: 10.1093/nar/gkx1121.
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Vertebral Fractures After Discontinuation of Denosumab: A Post Hoc Analysis of the Randomized Placebo-Controlled FREEDOM Trial and Its Extension.地舒单抗停药后发生的椎体骨折:一项 FREEDOM 随机安慰剂对照试验及其延伸的事后分析。
J Bone Miner Res. 2018 Feb;33(2):190-198. doi: 10.1002/jbmr.3337. Epub 2017 Nov 22.
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抗吸收药物对绝经后早期乳腺癌妇女的骨保护和辅助作用。

Antiresorptive agents' bone-protective and adjuvant effects in postmenopausal women with early breast cancer.

机构信息

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.

出版信息

Br J Clin Pharmacol. 2019 Jun;85(6):1125-1135. doi: 10.1111/bcp.13834. Epub 2019 Jan 25.

DOI:10.1111/bcp.13834
PMID:30536446
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6533425/
Abstract

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.

摘要

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。