nav emailalert searchbtn searchbox tablepage yinyongbenwen piczone journalimg journalInfo searchdiv qikanlogo popupnotification paper paperNew
2017 05 v.38;No.158 435-438+481
贝伐珠单抗联合化疗引起肾脏相关不良反应的临床观察

Summary

Note: Please note that the following content is generated by AI. CNKI does not take any responsibility related to this content.
基金项目(Foundation):
邮箱(Email):
DOI:
0 221 7
阅读 下载 被引

工具集

引用本文 下载本文
PDF
引用导出 分享

    扫码分享到微信或朋友圈

使用微信“扫一扫”功能。
将此内容分享给您的微信好友或者朋友圈
摘要:

目的观察晚期结直肠癌患者应用贝伐珠单抗联合化疗后出现高血压及蛋白尿的发生率。方法选取2012年1月至2016年12月我科收治的晚期结直肠癌患者64例,行贝伐珠单抗联合化疗。贝伐珠单抗用药:第1天予5 mg/kg静脉滴注30~90 min,以2周为1个周期;或第1天予7.5 mg/kg静脉滴注30~90 min,以3周为1个周期。应用贝伐珠单抗后定期监测血压,贝伐珠单抗每个周期给药前48 h内,行尿常规或24 h尿蛋白定量检查。结果贝伐珠单抗联合化疗后患者高血压发生率为26.6%,其中3级高血压发生率为7.8%,4级高血压发生率为1.6%。贝伐珠单抗联合化疗后患者蛋白尿的发生率为10.9%,其中3级蛋白尿的发生率为3.1%,无肾病综合征发生。结论贝伐珠单抗联合化疗不良反应发生率较低,安全性较好,使用该药过程中应定期监测及时处理发生的不良反应。

Abstract:

Objective To observe the adverse effects of bevacizumab combined with chemotherapy on the incidence of hypertension and proteinuria in the patients with advanced colorectal cancer. Methods Sixty-four patients with advanced colorectal cancer,who received medical care in our department of the hospital from January 2012 to December 2016,were enrolled for the study. The patients were treated with bevacizumab combined with chemotherapy. The treatment profiles of bevacizumab medication were: venous dropping at a dosage of 5 mg/kg for a duration of 30 ~ 90 minutes was administered the first day,with 2 weeks as a treatment cycle; or venous dropping at a dosage of 7. 5 mg/kg for a duration of 30 ~ 90 minutes was given the first day,with 3 weeks as a treatment cycle.Following medication of bevacizumab,blood pressure was detected regularly. Forty-eight hours before each treatment cycle,urine routines or 24 hour quantitative urine protein were detected. Results The incidence of hypertension for the patients treated with bevacizumab combined with chemotherapy was 26. 6%,of which the incidence of grade 3 hypertension was 7. 8% and that of grade 4 hypertension was 1. 6%. After combined treatment of bevacizumab and chemotherapy,the incidence of proteinuria was 10. 9%,of which the incidence of grade 3 proteinuria was 3. 1%,but without the occurrence of nephrotic syndromes. Conclusion Adverse drug reactions in the combined use of bevacizumab and chemotherapy were relatively low,with good safety. Nevertheless,regular monitoring of hypertension and proteinuria should be made for the sake of safety.

参考文献

[1]中华医学会消化内镜学分会,中国抗癌协会肿瘤内镜学专业委员会.中国早期结直肠癌筛查及内镜诊治指南(2014,北京)[J].中华医学杂志,2015,95(28):2235-2252.DOI:10.3760/cma.j.issn.0376-2491.2015.28.002.

[2]Vaziri SA,Kim J,Ganapathi MK,et al.Vascular endothelial growth factor polymorphisms:role in response and toxicity of tyrosine kinase inhibitors[J].Curr Oncol Rep,2010,12(2):102-108.DOI:10.1007/s11912-010-0085-4.

[3]Hurwitz H,Fehrenbacher L,Novotny W,et al.Bevacizumab plus irinotecan,fluorouracil,and leucovorin for metastatic colorectal cancer[J].N Engl J Med,2004,350(23):2335-2342.DOI:10.1056/NEJMoa032691.

[4]Saltz LB,Clarke S,Díaz-Rubio E,et al.Bevacizumab in combination with oxaliplatin-based chemotherapy as first-line therapy in metastatic colorectal cancer:a randomized phase III study[J].J Clin Oncol,2008,26(12):2013-2019.DOI:10.1200/JCO.2007.14.9930.

[5]Giantonio BJ,Catalano PJ,Meropol NJ,et al.Bevacizumab in combination with oxaliplatin,fluorouracil,and leucovorin(FOLFOX4)for previously treated metastatic colorectal cancer:results from the Eastern Cooperative Oncology Group Study E3200[J].J Clin Oncol,2007,25(12):1539-1544.DOI:10.1200/JCO.2006.09.6305.

[6]Hood JD,Meininger CJ,Ziche M,et al.VEGF upregulates ecNOS message,protein,and NO production in human endothelial cells[J].Am J Physiol,1998,274(3 Pt 2):H1054-H1058.

[7]Shen BQ,Lee DY,Zioncheck TF.Vascular endothelial growth factor governs endothelial nitric-oxide synthase expression via a KDR/Flk-1 receptor and a protein kinase C signaling pathway[J].J Biol Chem,1999,274(46):33057-33063.DOI:10.1074/jbc.274.46.33057.

[8]Mourad JJ,des Guetz G,Debbabi H,et al.Blood pressure rise following angiogenesis inhibition by bevacizumab.A crucial role for microcirculation[J].Ann Oncol,2008,19(5):927-934.DOI:10.1093/annonc/mdm550.

[9]Hayman SR,Leung N,Grande JP,et al.VEGF inhibition,hypertension,and renal toxicity[J].Curr Oncol Rep,2012,14(4):285-294.DOI:10.1007/s11912-012-0242-z.

[10]Sugimoto H,Hamano Y,Charytan D,et al.Neutralization of circulating vascular endothelial growth factor(VEGF)by anti-VEGF antibodies and soluble VEGF receptor 1(s Flt-1)induces proteinuria[J].J Biol Chem,2003,278(15):12605-12608.DOI:10.1074/jbc.C300012200.

[11]Gurevich F,Perazella MA.Renal effects of anti-angiogenesis therapy:update for the internist[J].Am J Med,2009,122(4):322-328.DOI:10.1016/j.amjmed.2008.11.025.

[12]Eremina V,Jefferson JA,Kowalewska J,et al.VEGF inhibition and renal thrombotic microangiopathy[J].N Engl J Med,2008,358(11):1129-1136.DOI:10.1056/NEJMoa0707330.

[13]Izzedine H,Massard C,Spano JP,et al.VEGF signalling inhibition-induced proteinuria:mechanisms,significance and management[J].Eur J Cancer,2010,46(2):439-448.DOI:10.1016/j.ejca.2009.11.001.

[14]Zhu X,Wu S,Dahut W L,et al.Risks of proteinuria and hypertension with bevacizumab,an antibody against vascular endothelial growth factor:systematic review and meta-analysis[J].Am J Kidney Dis,2007,49(2):186-193.DOI:10.1053/j.ajkd.2006.11.039.

基本信息:

DOI:

中图分类号:R979.1

引用信息:

[1]李小影,陈建胜,潘景业.贝伐珠单抗联合化疗引起肾脏相关不良反应的临床观察[J].海军医学杂志,2017,38(05):435-438+481.

基金信息:

文档文件

引用

GB/T 7714-2015 格式引文
MLA格式引文
APA格式引文