Department of Medicine, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.
Clin Cancer Res. 2010 Aug 15;16(16):4084-93. doi: 10.1158/1078-0432.CCR-10-0600. Epub 2010 Jul 19.
Most patients with bone metastases experience skeletal complications, resulting in significant morbidity and increased risk of death. Although the use of bisphosphonates is a well-established form of supportive care treatment for bone metastasis, complications arising from long-term use require schedule optimization and a search for alternative strategies. Moreover, the scope of use of bone-targeted agents in oncology has widened to include therapy-induced bone loss and antitumor effects. Indeed, bone provides a permissive niche to tumor growth, and targeting the interactions within the bone microenvironment is a promising antitumor strategy. In addition, the pathogenesis of cancer-related bone disease has been partially unraveled with a focus on the anabolic bone compartment, and the rapid bench-to-bedside translation has resulted in the identification of novel therapeutically amenable targets. This review focuses on studies optimizing bisphosphonate use and recent clinical data on denosumab in the treatment of bone disease. We also provide data on trials that have evaluated the antitumor effects of bisphosphonates and summarize the most recent discoveries on the role of the bone niche in cancer development, with insights into the preclinical rationale and clinical assessment of novel antiresorptive and anabolic bone-targeted agents.
大多数患有骨转移的患者都会出现骨骼并发症,从而导致严重的发病率和死亡率增加。尽管双膦酸盐的使用是一种经过充分验证的骨转移支持性治疗方法,但长期使用所引起的并发症需要对治疗方案进行优化,并寻找替代策略。此外,骨靶向药物在肿瘤学中的应用范围已经扩大,包括治疗引起的骨丢失和抗肿瘤作用。事实上,骨骼为肿瘤生长提供了一个有利的微环境,靶向骨骼微环境中的相互作用是一种很有前途的抗肿瘤策略。此外,癌症相关骨病的发病机制已经部分阐明,重点是合成代谢性骨区,快速的从实验室到临床的转化导致了新的治疗靶点的确定。本综述重点介绍了优化双膦酸盐使用的研究以及在治疗骨疾病中地舒单抗的最新临床数据。我们还提供了关于评估双膦酸盐抗肿瘤作用的试验数据,并总结了骨骼微环境在癌症发展中的最新发现,包括对新型抗吸收和合成代谢性骨靶向药物的临床前原理和临床评估的深入了解。