Coleman Robert, Brown Janet, Terpos Evangelos, Lipton Allan, Smith Matthew R, Cook Richard, Major Pierre
Academic Unit of Clinical Oncology, Cancer Research Centre, Weston Park Hospital, Sheffield S10 2SJ, UK.
Cancer Treat Rev. 2008 Nov;34(7):629-39. doi: 10.1016/j.ctrv.2008.05.001. Epub 2008 Jun 24.
Bone metastases are prevalent among patients with advanced solid tumors. Metastatic bone disease alters bone homeostasis, resulting in reduced bone integrity and, consequently, increased skeletal complications. Biochemical markers of bone metabolism may meet an unmet need for useful, noninvasive, and sensitive surrogate information for following patients' skeletal health.
Data for this review were identified by searches of PubMed, and references from relevant articles using the search terms "bone markers" or individual bone marker nomenclature, "cancer," and "metastases." Abstracts and reports from meetings were included only when they related directly to previously published work. Only papers published in English between 1990 and 2007 were included.
Recent retrospective analyses with bisphosphonates, and particularly with zoledronic acid, have shown significant correlations between biochemical markers of bone metabolism levels and clinical outcomes, especially for bone resorption markers. Clinical results for biochemical markers of bone formation and resorption and other emerging markers of bone metabolism including bone sialoprotein, receptor-activator of nuclear factor-kappaB ligand, osteoprotegerin, and other markers are presented. However, biochemical markers of bone metabolism are not yet an established surrogate endpoint for treatment efficacy.
Biochemical markers of bone metabolism may allow physicians to identify which patients with metastatic bone disease are at high risk for skeletal-related events or death and who may be responding to therapy. Prospective randomized clinical trials are underway to further assess the utility of markers of bone metabolism in patients with bone metastases.
骨转移在晚期实体瘤患者中很常见。转移性骨病会改变骨稳态,导致骨完整性降低,进而增加骨骼并发症。骨代谢的生化标志物可能满足对有用、非侵入性且敏感的替代信息的未满足需求,用于跟踪患者的骨骼健康状况。
通过检索PubMed以及使用搜索词“骨标志物”或单个骨标志物名称、“癌症”和“转移”从相关文章中获取参考文献来确定本综述的数据。仅当会议摘要和报告与先前发表的工作直接相关时才纳入。仅纳入1990年至2007年间以英文发表的论文。
近期对双膦酸盐,特别是唑来膦酸的回顾性分析表明,骨代谢水平的生化标志物与临床结果之间存在显著相关性,尤其是对于骨吸收标志物。展示了骨形成和骨吸收的生化标志物以及其他新兴骨代谢标志物(包括骨唾液蛋白、核因子-κB受体激活剂配体、骨保护素和其他标志物)的临床结果。然而,骨代谢的生化标志物尚未成为治疗疗效的既定替代终点。
骨代谢的生化标志物可能使医生能够识别哪些转移性骨病患者发生骨骼相关事件或死亡的风险较高,以及哪些患者可能对治疗有反应。正在进行前瞻性随机临床试验,以进一步评估骨代谢标志物在骨转移患者中的效用。