期刊文献+

分次小剂量奈达铂联合氟尿嘧啶治疗晚期食管癌的临床观察 被引量:6

Clinical observation of multiple low doses of nedaplatin(NDP) combined with continuous intravenous infusion of 5-fluorouracil(5-FU) in the treatment of advanced esophageal cancer
下载PDF
导出
摘要 目的:观察分次小剂量奈达铂(NDP)联合5-氟尿嘧啶(5-FU)持续静滴治疗晚期食管癌的近期疗效及不良反应。方法:将55例晚期食管癌患者随机分入实验组和对照组,实验组28例,给予NDP 20mg/m2静脉滴注,d1-5,5-FU 1.5/m2,化疗泵持续静脉输注120小时;对照组27例,给予NDP 100mg/m2静脉滴注,d1,5-FU用法同实验组。两组均21天为1周期。结果:实验组总有效率为(46.4%),对照组总有效率为(51.9%),两组比较无显著性差异(P>0.05)。实验组骨髓抑制的发生率明显低于对照组(P<0.05),消化道毒性及肾毒性两组无明显差异。结论:分次小剂量NDP联合5-FU持续滴注治疗晚期食管癌疗效确切,骨髓抑制及消化道反应均较轻,患者耐受良好。可考虑分次小剂量NDP给药方法替代常规奈达铂的用法。 Objective:To observe the short-term efficacy and adverse reaction of multiple low dose of nedaplatin(NDP) combined with continuous intravenous infusion of 5-fluorouracil(5-FU) in the treatment of advanced esophageal cancer.Methods: Fifty-five patients with advanced esophageal cancer were divided into experimental group and control group randomly.The experimental group,with 28 cases,was given NDP 20 mg/m2,intravenous drip,d1-5,5-FU 1.5/m2,continuous infusion for 120 hours,with chemotherapy pump;the control group with 27 cases was given NDP 100mg/m2,intravenous drip,d1,the usage of 5-FU was the same as the experimental group.Both 5-FU groups were treated every 21 days as a cycle.Results: The total effective rate of the experimental group was(46.4%),the control group was(51.9%),there was no significant difference between two groups(P 0.05).The rate of myelosuppression of the experimental group was lower than that in the control group,the difference was significant(P0.05),the rates of alimentary canal toxicity and nephrotoxicity had no significant differences between the two groups.Conclusion: Multiple low doses of nedaplatin(NDP) combined with continuous intravenous infusion of 5-fluorouracil(5-FU) in the treatment of advanced esophageal cancer is effective,myelosuppression and gastrointestinal reaction are mild,patients can tolerate it well.Multiple low doses of nedaplatin can be considered to replace the normal usage of nedaplatin(NDP).
出处 《现代肿瘤医学》 CAS 2012年第12期2534-2536,共3页 Journal of Modern Oncology
关键词 奈达铂 分次小剂量 食管癌 晚期 nedaplatin multiple small dose esophagus carcinoma advanced
  • 相关文献

参考文献13

  • 1Eisenhauer EA, Therasse P, Bogaerts J, et al. New response eval-uation criteria in solid tumours : revised RECIST guideline (version1.1) [ J]. Eur J Cancer,2009,45(2) :228 -247.
  • 2Trotti A, Colevas AD, Setser A, et al. CTCAE v3.0 : developmentof a comprehensive grading system for the adverse effects of cancertreatment[ J]. Semin Radiat Oncol,2003 ,13(3) : 176 -181.
  • 3Ajani JA. Contributions of chemotherapy in the treatment of carci-noma of the esophagus: results and commentary[ J]. Semin Oncol,1994,21(4):474 -482.
  • 4Desoize B, Madoulet C. Particular aspects of platinum compoundsused at present in cancer treatment [ J]. Crit Rev Oncol Hematol,2002,42(3) :317 -325.
  • 5张姣,沙晓峰,韦淑贞,杨青梅,张闯.放疗联合奈达铂、氟尿嘧啶治疗食管癌的疗效观察[J].现代肿瘤医学,2010,18(2):307-309. 被引量:6
  • 6管忠震,徐瑞华.奈达铂临床研究进展[J].中国肿瘤临床,2004,31(13):774-780. 被引量:176
  • 7Rougier P, Paillot B, Laplanche A, et al. 5 - Fluorouracil (5 -FU) continuous intravenous infusion compared with bolus adminis-tration, Final results of a randomised trial in metastatic colorectalcancerf J] . Eur J Cancer, 1997,33 (11) ; 1789 - 1793.
  • 8Group In Cancer. Efficacy of intravenous continuous infusion of flu-orouracil compared with bolus administration in advanced colorectalcancer. Meta - analysis [ J]. J Clin Oncol,1998,16(1) :301 -308.
  • 9Furukawa S, Yoshida T,Tukuda M, et al. Experimental study oncombination chemotherapy with platinum compounds and 5 - flu-orouracil [J]. Gan To Kagaku Ryoho, 1989,16(3 Pt 1) :419 -422.
  • 10张从军,闫敏,孟琼.紫杉醇联合DDP与奈达铂联合5-FU治疗晚期食管癌的临床观察[J].现代肿瘤医学,2010,18(1):74-76. 被引量:18

二级参考文献57

共引文献229

同被引文献47

  • 1Ze-Tian Shen,Xin-Hu Wu,Bing Li,Jun-Shu Shen,Zhen Wang,Jing Li,Xi-Xu Zhu.Nedaplatin concurrent with three-dimensional conformal radiotherapy for treatment of locally advanced esophageal carcinoma[J].World Journal of Gastroenterology,2013,19(48):9447-9452. 被引量:23
  • 2邓可刚.循证医学证据的检索步骤与检索系统的选择[J].中国循证医学杂志,2004,4(9):634-637. 被引量:26
  • 3章宏,厉有名,虞朝辉,王升启,季峰,陈春晓.肿瘤患者二氢嘧啶脱氢酶基因多态性与5-氟尿嘧啶毒副反应的关系[J].中华内科杂志,2007,46(2):103-106. 被引量:14
  • 4Holma R, Korpela R, Sairanen U, et al. Colonic methane produc- tion modifies gastrointestinal toxicity associated with adjuvant 5- Fluorouracil chemotherapy for colorectal cancer [ J ]. J Clin Gastro- enterol, 2013,47( 1 ) :45-51.
  • 5Li J, Hou N, Faried A, et al. IInhibition of autophagy augments 5- fluorouracil chemotherapy in human colon cancer in vitro and in vi- vo model [ J ]. Eur J Cancer, 2010,46 (10) : 1900-1909.
  • 6Di Paolo A, Lencioni M, Amatori F, et al. 5-fluorouracil pharma- cokinetics predicts disease-free survival in patients administered adjuvant chemotherapy for colorectal cancer [ J]. Clin Cancer Res, 2008,14(9) :2749-2755.
  • 7Schwab M, Zanger UM, Marx C, et al. Role of genetic and nonge- netic factors for fluorouracil treatment-related severe toxicity : a pro- spective clinical trial by the German 5-FU Toxicity Study Group [J]. J Clin Oncol, 2008,26(13) :2131-2138.
  • 8Teh LK, Hamzab S, Hashim H, et al. Potential of dihydropyrimi- dine dehydrogenase genotypes in personalizing 5-Fluorouracil thera- py among eolorectal cancer patients [ J]. Ther Drug Monit, 2013, 35 (5) :624-630.
  • 9Kaldate RR, Haregewoin A, Gricr CE, et al. Modeling the 5-flu- orouracil area under the curve versus dose relationship to develop apharmacokinetic dosing algorilhm for colorectal cancer patients re- ceiving FOLFOX6 [ J ]. Oncologist, 2012,17 ( 3 ) : 296 -302.
  • 10Kristensen MH, l%dersen PL, Melsen GV, et al. Variants in the dihydropyrimidine dehydrogenase, methylenetetrahydrofolate reduc- tase and thymidylate synthase genes predict early toxicity of 5-flu- orouracil in colorectal cancer patients [ J]. J Int Med Res, 2010, 38(3) :870-883.

二级引证文献38

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