期刊文献+

行 AC-T 序贯治疗乳腺癌化疗方案患者多西他赛血药浓度监测的临床价值 被引量:4

Clinical value of monitoring of plasma docetaxel concentration in patients with breast cancer in AC -T sequential chemotherapy
原文传递
导出
摘要 目的:研究乳腺癌患者化疗后,多西他赛(DTX)血药浓度与疗效及毒副作用的相关性。方法选择湖北省肿瘤医院2015年4-9月接受 AC-T 序贯治疗方案一线化疗的71例乳腺癌患者为研究对象。用胶乳免疫比浊法于每周期 DTX 静脉输注后检测其血药浓度。根据血药浓度分布分为≤2.0 mg·h^-1·L^-1组(A 组)、〉2.0-2.5 mg·h^-1·L^-1组(B 组)和〉2.5 mg·h^-1·L^-1组(C 组),采用χ^2检验回顾性分析血药浓度与不良反应程度、疗效之间的相关性。结果A 组、B 组、C 组 DTX 血药浓度分别为(1.55±0.36)mg·h^-1·L^-1、(2.28±0.13)mg·h^-1·L^-1、(2.87±0.38)mg·h^-1·L^-1。随着 DTX 血药浓度的升高,化疗的毒副作用程度加强(χ^2=5.169、4.463、3.630,P =0.023、0.035、0.047)。B、C 组总有效率均为95.8%,高于 A 组的87.0%,差异无统计学意义(χ^2=1.559,P =0.240)。结论DTX 的血药浓度在2.1-2.5 mg·h^-1·L^-1的乳腺癌患者疗效较好,且毒副反应能控制在一定程度内。 Objective To investigate the relationship between plasma docetaxel concentration and the efficacy as well as toxic and side effects in patients with breast cancer after chemotherapy.Methods Seventy -one patients with breast cancer who accepted AC sequential T chemotherapy regimen as first line treatment were selected from April 2015 to September 2015 in Hubei Provicial Tumor Hospital.The plasma concentration of docetaxel was detected by latex immunoturdidimetry after the docetaxel continuous infusion in each cycle.The three groups were assigned according to the concentration distribution of docetaxel:group A (plasma concentration docetaxel ≤ 2.0mg·h^-1 · L^-1 ),group B (2.1 -2.5mg·h^-1 ·L^-1 )and group C (≥2.6 mg·h^-1 ·L^-1 ).The relationship between the drug plasma concentration,therapeutic efficacy and adverse reactions in different docetaxel plasma concentration was analyzed retrospectively by Chi -square tests.Results The average plasma concentrations of docetaxel of the three groups were (1.55 ±0.36)mg·h^-1 ·L^-1 ,(2.28 ±0.13)mg·h^-1 ·L^-1 ,(2.87 ±0.38)mg· h^-1 · L^-1 respectively.The adverse reactions were enhanced with the increasing of docetaxel plasma concentration (χ^2 =5.169, 4.463,3.630,P =0.023,0.035,0.047).The therapeutic efficacy of group C and group B was same(95.8%),which was higher than 87.0% of group A,but there was no statistically significant difference (χ^2 =1.559,P =0.24). Conclusion Breast cancer patients whose plasma concentration of docetaxel is between 2.1 -2.5mg·h^-1 ·L^-1 has a better prognosis,and its adverse reactions are controlled in a certain extent.
作者 喻晶 郑红梅 袁峰 潘翠萍 Yu Jing Zheng Hongmei Yuan Feng Pan Cuiping(Department of Clinical Laboratory ,Hubei Provicial Tumor Hospital, Wuhan, Hubei 430079, China Department of Galactophore, Hubei Provicial Tumor Hospital, Wuhan, Hubei 430079, China)
出处 《中国基层医药》 CAS 2017年第5期689-692,J0001,共5页 Chinese Journal of Primary Medicine and Pharmacy
关键词 乳腺肿瘤 多西他赛 药物监测 Breast Neoplasms Docetaxel Drug Monitoring
  • 相关文献

参考文献10

二级参考文献102

  • 1中国抗癌协会乳腺癌专业委员会.中国抗癌协会乳腺癌诊治指南与规范(2011版)[J].中国癌症杂志,2011,21(5):367-417. 被引量:265
  • 2夏维,秦仁义.大鼠胰腺癌细胞系R-PC的建立及其生物学特性[J].中华实验外科杂志,2006,23(6):692-694. 被引量:2
  • 3Rivera E,Gomez H.Chemotherapy resistance in metastatic breast cancer:the evolving role of ixabepilone.Breast Cancer Res,2010,12 (Suppl 2):2.
  • 4Martin M,Pienkowski T,Mackey J,et al.Adjuvant docetaxel for nodepositive breast cancer.N Engl J Med,2005,352:2302-2313.
  • 5Kakumoto M,Sakaeda T,Takara K,et al.Effects of carvedilol on MDR1-mediated multidrug resistance:comparison with verapamil.Cancer Sci,2003,94:81-86.
  • 6Takeshita A,Shigeno K,Shinjo K,et al.All-trans retinoic acid (ATRA) differentiates acute promyelocytic leukemia cells independently of P-glycoprotein (P-gp) related multidrug resistance.Leuk Lymphoma,2001,42:739-746.
  • 7Tanei T,Morimoto K.Shimazu K,et al.Association of breast cancer stem cells identified by aldehyde dehydrogenase 1 expression with resistance to sequential Paclitaxel and epirubicin-based chemotherapy for breast cancers.Clin Cancer Res,2009,15:42344241.
  • 8李书玲.乳腺肿瘤学[M].北京:科学技术文献出版社,2000:628.
  • 9Rivera E, Gomez H. Chemotherapy resistance in metastatic breast canc-er: the evolving role of ixabepilone [ J ]. Breast Cancer Res, 2010,12(Suppl 2) :S2.
  • 10Martin M,Pienkowski T,Mackey J,et al. Adjuvant docetaxel for node-positive breast cancer [ J]. N Engl J Med, 2005, 352 ( 22 ) : 2302-2313.

共引文献65

同被引文献28

引证文献4

二级引证文献10

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