期刊文献+

285例新型抗肿瘤药物不良反应分析 被引量:2

285 cases of adverse drug reaction related to new antineoplastic drugs
下载PDF
导出
摘要 目的 研究新型抗肿瘤药物的药品不良反应(ADR)的发生规律及特点,为临床安全用药提供参考。方法 对某三甲综合医院2018年1月1日至2023年3月31日新型抗肿瘤药物致ADR共285例,对患者性别、年龄、超说明书用药、ADR累及系统-器官和临床表现、ADR分级与转归、关联性评价等进行回顾性统计分析。结果 285例ADR男性155例(54.39%),女性130例(45.61%),平均年龄(54.98±13.175)岁;临床表现426例次,累及系统-器官12个,最常见的为消化系统(44.13%)、血液及造血系统(19.01%);严重ADR 51例,新的ADR 6例。涉及新型抗肿瘤药物33种,其中国家医保谈判药物28种,共266例次,大分子单体克隆药物特别是免疫检查点抑制剂的ADR较多,ADR例数最多的是卡瑞利珠单抗(66例)。涉及超说明书用药118例,超说明书用药的ADR发生率为63.10%。结论 新型抗肿瘤药物相关的ADR可发生于各个年龄,累及多个器官-系统,严重ADR较多,新的ADR较少,超说明书用药相关ADR较多;建议通过多学科联合会诊(MDT)、超说明书备案等措施严格管理超说明书用药,加强用药教育和药学监护,提高用药的安全性和有效性。 Objective To study the patterns and characteristics of adverse reaction(ADR)related to new antineoplastic drugs,and provide reference for clinical medication.Methods A total of 285 cases of ADR caused by new antineoplastic drugs were collected in a tertiary general hospital from January 2018 to March 2023.The data on the gender,age,systemsorgans involved in ADR,clinical manifestations,off-label medication,grading and outcomes of ADR and correlations was analyzed via the Microsoft Excel and SPSS software.Results Among the 285 cases of ADR,155(54.39%)involved males and 130(45.61%)involved females,and the average age was(54.98±13.175)years.There were 426 cases of clinical manifestations and 12 systems-organs were involved.The digestive system(44.13%)and blood and hematopoietic system(19.01%)were more vulnerable.There were 51 cases of severe ADR,and 6 cases of new general ADR.There were 33 new anti-tumor drugs involved.Macromolecular monoclonal drugs,especially immune checkpoint inhibitors,caused more ADR,among which carrelizumab caused the largest number of cases(66 cases).One hundred and eighteen of these cases involved off-label medication,and the rate was as high as 63.10%.Conclusion ADR associated with novel antineoplastic drugs can occur among patients of any age,and involve multiple organs-systems.New antineoplastic drugs induce more serious ADR than new ADR,and many of these ADR are related to off-label drug use.It is recommended that off-label drug use be adopted,pharmaceutical care provided,and the safety and effectiveness of drug use improved for patients.
作者 徐伟佳 彭崎 黄海渝 张磊姣 肖华 吴雪 XU Weijia;PENG Qi;HUANG Haiyu;ZHANG Leijiao;XIAO Hua;WU Xue(Department of Pharmacy,the 924th Hospital of Joint Logistic Support Force,Guilin Guangxi 541002,China;Department of Oncology,the 924th Hospital of Joint Logistics Support Force,Guilin Guangxi 541002,China)
出处 《中国药物警戒》 2024年第2期199-203,210,共6页 Chinese Journal of Pharmacovigilance
基金 广西药学会医院药学科研项目(GXYXH1-202212)。
关键词 新型抗肿瘤药物 药品不良反应 超说明书用药 国家医保谈判 大分子单体克隆药 消化系统 血液及造血系统 new antineoplastic drugs adverse drug reaction off-label medication national medical insurance negotiation macromolecular monoclonal drugs digestive system blood and hematopoietic system
  • 相关文献

参考文献9

二级参考文献126

  • 1Izzedine H, Massard C, Spano JP, et al. VEGF signalling inhibi- tion-induced proteinuria: Mechanisms, significance and manage- ment[J]. Eur J Cancer, 2010, 46(2) : 439-448.
  • 2Yang JC, Haworth L, Sherry RM, et al. A randomized trial of be- vacizumab, an anti-vascular endothelial growth factor antibody, for metastatic renal cancer [ J ]. N Engl J Med, 2003, 349 ( 5 ) : 427-434.
  • 3Takahashi D, Nagahama K, Tsuura Y, et al. Sunitinib-induced nephrotic syndrome and irreversible renal dysfunction [ J ]. Clin Exp Nephrol, 2012, 16(2) : 310-315.
  • 4Wu S, Kim C, Baer L, et al. Bevacizumab increases risk for se- vere proteinuria in cancer patients[ .11. J Am Soc Nephrol, 2010, 21(8) : 1381-1389.
  • 5Fangnsaro J, Gururangan S, Poussaint TY, et al. Bevacizumab (BVZ)-associated toxicities in children with recurrent central nervous system tumors treated with BVZ and irinotecan (CPT- 11): a Pediatric Brain Tumor Consortium Study (PBTC-022) [J]. Cancer, 2013, 119(23): 4180-4187.
  • 6Sclafani F, Cunningham D. Bevaeizumab in elderly patients with metastatic eolorectal cancer[ J]. J Geriatr Oneol, 2014, 5 ( 1 ) : 78-88.
  • 7Isobe T, Uchino K, Makiyama C, et al. Analysis of adverse events of bevaeizumab-containing systemic chemotherapy for meta- static colorectal cancer in Japan[ J]. Anticancer Res, 2014, 34 (4) : 2035-2040.
  • 8Lockhart AC, Rothenberg ML, Dupont J, et al. Phase I study of intravenous vascular endothelial growth factor trap, aflibercept, in patients with advanced solid tumors[ J ]. J Clin Oncol, 2010, 28 (2) : 207-214.
  • 9Tang PA, Cohen SJ, Kollmannsberger C, et al. Phase 1I clinical and pharmacokinetic study of aflibercept in patients with previously treated metastatic colorectal cancer [ J ]. Clin Cancer Res, 2012, 18(21): 6023-6031.
  • 10Van Cutsem E, Tabemero J, Lakomy R, et al. Addition of aflibercept to lluorouracil, leucovorin, and irinotecan improves survival in a phase IR randomized trial in patients with metastatic colorectal cancer previously treated with an oxaliplatin-based regi- men[J]. J Clin Oncol, 2012, 30(28) : 3499-3506.

共引文献932

同被引文献29

引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部