临床肿瘤学杂志

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血清β-CTX和OST在骨转移放疗中的临床研究

徐欣,黄仁华,周狄,马秀梅,叶明,白永瑞   

  1. 200127 上海 上海交通大学医学院附属仁济医院放疗科
  • 收稿日期:2012-09-26 修回日期:2012-11-11 出版日期:2013-01-31 发布日期:2013-01-31
  • 通讯作者: 白永瑞

Clinical value of serum β-CTX and osteocalcin in bone metastases radiotherapy

XU Xin, HUANG Renhua, ZHOU Di, MA Xiumei, YE Ming, BAI Yongrui   

  1. Department of Radiotherapy, Renji Hospital Affiliated to Medical School of Shanghai Jiaotong University, Shanghai 200127, China
  • Received:2012-09-26 Revised:2012-11-11 Online:2013-01-31 Published:2013-01-31
  • Contact: BAI Yongrui

摘要: 目的 探讨骨转移患者放疗前、后血清中骨钙素(OST)和Ⅰ型胶原羧基端肽β特殊序列(β-CTX)水平的变化及与临床病理特征、放疗疗效的关系。方法 采用电化学发光法定量检测34例骨转移患者血清中β-CTX和OST的表达水平,分析其与骨转移患者临床病理特征的关系。将34例患者分为单纯放疗组和放疗+膦酸盐组,观察两组放疗前、后血清β-CTX和OST水平的变化及其与放疗疗效的关系。结果 34例患者治疗前血清中OST、β-CTX的表达水平分别为(17.07±9.03)ng/ml和(593.94±319.26)pg/ml。血清β-CTX水平与骨转移程度分级、骨相关事件及软组织肿块相关(P<0.05),而与骨转移类型、骨痛程度无关(P>0.05);血清OST水平与临床病理特征均无关。在单纯放疗组中,放疗后血清β-CTX水平较放疗前升高(P<0.05),在放疗+膦酸盐组中则较放疗前明显下降(P<0.05);两组血清OST水平放疗前、后比较,差异均无统计学意义(P>0.05)。治疗有效组治疗前血清β-CTX和OST水平均低于无效组(P<0.05)。分层分析显示,在放疗+膦酸盐组中,无论治疗是否有效血清β-CTX水平较治疗前下降(P<0.05),而血清OST水平治疗前后无明显变化(P>0.05);在单纯放疗组中,放疗后血清β-CTX水平在无效组中明显升高(P<005),而在有效组中轻度升高(P>0.05),血清OST水平放疗前后无明显差异(P>0.05)。结论 血清β-CTX水平的检测有助于骨转移患者的病情判断及放疗疗效的预测,在临床上具有一定的应用价值。

Abstract: Objective To investigate the level of β-C-terminal telopeptide of type Ⅰ collagen(β-CTX)and osteocalcin (OST) in patients with bone metastases before and after radiotherapy and their correlation with clinicopathological characteristics and response to radiotherapy. Methods The serum OST and β-CTX in 34 patients with bone metastases were tested by electrochemiluminescence immunoassay. The relation between the level of OST, β-CTX and clinicopathological characteristics were assessed. Thirty-four patients were divided into two groups, one group received only radiation of bone metastases and the other group was treated with radiation+zoledronic acid. The correlation between the level of serum OST, β-CTX before and after radiotherapy and the response to radiotherapy were analyzed. Results The levels of serum OST and β-CTX in 34 patients before treatment were(17.07±9.03)ng/ml and(593.94± 319.26)pg/ml, respectively. The serum β-CTX had correlation with the grade of bone metastases, skeletal related events and soft tissue mass, but not related to type of bone metastases and degree of metastatic bone pain, while the OST level was not correlated with clinicopathological characteristics. The level of βCTX after treatment in radiotherapy group was higher than that before radiotherapy (P<0.05), while in radiotherapy+zoledronic acid group was lower than that before treatment (P<0.05), and the level of OST before and after treatment had no significant difference (P>0.05). The levels of β-CTX and OST before treatment in effective group were lower than those in ineffective group (P<0.05). The β-CTX levels decreased after treatment in radiotherapy+zoledronic acid group no matter how the efficacy was. The βCTX levels increased in the nonresponding patients treated with radiotherapy alone (P<0.05), and the increase was not statistically significant in the responder (P>0.05).The OST levels in the two groups showed no change after radiotherapy (P>0.05). Conclusion The levels of bone metabolic marker β-CTX have important significance in disease condition evaluation and radiation efficacy prediction of bone metastases with application values in clinical practice.

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