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心肌生化标志物联合检测评价重组人血管内皮抑素心脏毒性
引用本文:覃晶,张鹏海,钱新宇,康世均,罗荣城,王月刚.心肌生化标志物联合检测评价重组人血管内皮抑素心脏毒性[J].南方医科大学学报,2008,28(6):930-933.
作者姓名:覃晶  张鹏海  钱新宇  康世均  罗荣城  王月刚
作者单位:1. 南方医科大学南方医院肿瘤科,广东,广州,510515
2. 南方医科大学南方医院心内科,广东,广州,510515
摘    要:目的 评价肌酸激酶同工酶(CK-MB)、肌钙蛋白T(cTnT)和N端B型脑钠肽(NT-proBNP)三种心肌生化标志物以及心电图在监测重组人血管内皮抑素心脏毒性中的临床意义.方法 将48例恶性肿瘤患者分成两组,A组(24例)重组人血管内皮抑素联合化疗,B组(24例)单纯化疗,每治疗周期的d0、d15,检测心电图,以及血清CK.MB、cTnT和血浆中NT-proBNP水平,共观察2个治疗周期.结果A组每个治疗周期结束后CK-MB,cTnT和NT-proBNP与治疗前基线相比明显升高(P<0.05),B组组内比较则无统计学差异(P>0.05);两组治疗前(基线)CK-MB,cTnT和NT-proBNP水平无统计学差异(P>0.05),每个周期治疗后A组CK-MB,cTnT和NT-proBNP水平与B组相比均有明显升高,有统计学差异(P,0.05).A组组内不同治疗时间心电图异常率比较有统计学差异(P<0.05),第二周期治疗后心电图异常率两组相比有统计学差异(P<0.05).结论 重组人血管内皮抑素存在确切的心脏毒性.CK-MB、cTnT和NT-proBNP可作为预测重组人血管内皮抑素心脏毒性的心肌生化标志物.

关 键 词:重组人血管内皮抑素  心脏毒性  心肌标志物  心肌生化标志物  检测评价  重组人血管内皮抑素  心脏毒性  cancer  patients  biochemical  markers  myocardial  endostatin  human  recombinant  预测  存在  异常率  治疗时间  统计学差异  比较  基线  结果  水平  血浆
文章编号:1673-4254(2008)06-0930-03
修稿时间:2008年1月15日

Assessment of the cardiotoxicity of recombinant human endostatin using myocardial biochemical markers in cancer patients
QIN Jing,ZHANG Peng-hai,QIAN Xin-yu,KANG Shi-jun,LUO Rong-cheng,Wang Yue-gang.Assessment of the cardiotoxicity of recombinant human endostatin using myocardial biochemical markers in cancer patients[J].Journal of Southern Medical University,2008,28(6):930-933.
Authors:QIN Jing  ZHANG Peng-hai  QIAN Xin-yu  KANG Shi-jun  LUO Rong-cheng  Wang Yue-gang
Institution:Department of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. qinjing_abc @yahoo.com.cn
Abstract:OBJECTIVE: To evaluate the value of the myocardial biochemical markers including creatine kinase MB isoenzyme (CK-MB), cardiac isoform of Tropnin-T (cTnT) and N-termimal pro-brain natriuretic peptide (NT-proBNP) and electrocardiogram (ECG) in monitoring the cardiotoxicity of recombinant human endostatin (rh-endostatin) in cancer patients. METHODS: Forty cancer patients were divided into two groups and received rh-endostatin in addition to chemotherapy (group A, n=24) or chemotherapy only (Group B, n=24). Serum CK-MB, cTnT levels and plasma NT-proBNP levels were measured and the ECG was recorded in all the patients before and after each of the two therapy cycles. RESULTS: In group A, serum CK-MB, cTnT and plasma NT-proBNP levels were significantly increased after the treatment in comparison with the baseline levels (P<0.05), but such increment was not observed in group B (P>0.05). With comparable baseline levels of CK-MB, cTnT and NT-proBNP before the treatment (P>0.05), patients in group A showed significantly higher levels of the indices than those in group B after each therapy cycle (P<0.05). Increased ECG abnormality were observed after rh-endostatin treatment in Group A (P<0.05) at a rate significantly higher than that of Group B after the second treatment cycle (P<0.05). CONCLUSION: Rh-endostatin has definite cardiotoxicity, and detection of the myocardial biochemical markers of CK-MB, cTnT and NT-proBNP may help predict the occurrence of cardiotoxicity.
Keywords:recombinant human endostatin  cardotoxicity  myocardial markers  
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