期刊文献+

培美曲赛和长春瑞滨分别联合顺铂一线治疗晚期肺腺癌的临床研究 被引量:11

下载PDF
导出
摘要 目的:对比培美曲塞与长春瑞滨分别联合顺铂在一线治疗晚期肺腺癌患者中的近期疗效和不良反应。方法:56例Ⅲ~Ⅳ期经病理组织学和(或)细胞学检查确诊的肺腺癌患者,培美曲赛组25例,长春瑞滨组31例。分别给予培美曲赛联合顺铂方案和长春瑞滨联合顺铂方案治疗。结果:两组客观缓解率和疾病控制率差异均无统计学意义(P>0.05);Ⅲ~Ⅳ级血液学毒性反应发生率培美曲赛组低于对长春瑞滨组,差异有统计学意义(P<0.05)。结论:培美曲塞联合顺铂一线治疗晚期肺腺癌的疗效与长春瑞滨联合顺铂近期的疗效相似,毒副反应较轻。
出处 《实用医学杂志》 CAS 北大核心 2013年第3期463-465,共3页 The Journal of Practical Medicine
基金 云南省社会发展重点项目(编号:2010CA015) 云南省科技厅社会发展科技计划应用基础研究项目(编号:2009ZC120M)
  • 相关文献

参考文献13

  • 1李进.肿瘤内科诊治策略[M]上海:上海科学技术出版社,201049-63.
  • 2苏珊,吕江青,李宁,张贤兰.培美曲塞与吉西他滨联合铂类一线治疗晚期肺腺癌的临床疗效观察[J].实用医学杂志,2011,27(8):1458-1460. 被引量:39
  • 3Gronberg B H,Bremnes R M. Phase Ⅲ study by the Norwegian lung cancer study group:pemetrexed pluscarboplatin compared with gemcitabine plus carboplatin as first-line chemotherapy in advanced non-small-cell lung cancer[J].Journal of Clinical Oncology,2009,(19):3217-3224.doi:10.1200/JCO.2008.20.9114.
  • 4鲍云华,李俭杰.介绍新的实体瘤治疗反应评价标准(RECIST)[J].中国肺癌杂志,2005,8(1):77-78. 被引量:108
  • 5孙燕;石远凯.临床肿瘤内科手册[M]北京:人民卫生出版社,2009826-830.
  • 6Adjei A. Pharmacology and mechanism of action of pemetrexed[J].Clinical Lung Cancer,2004,(01):51-55.
  • 7李树婷,马飞,孙燕.抗肿瘤代谢新药——培美曲塞[J].癌症进展,2005,3(5):471-476. 被引量:73
  • 8Vogcixang N J,Rusthovcn I I,Symanowski I. Phase Ⅲ study of pemetrexed combination with cisplatin versuscisplatin alone in patients with malignant pleural mesothelioma[J].Journal of Clinical Oncology,2003,(14):2636-2644.
  • 9Scaglioti G,Parikh P,von Pawel J. Phase Ⅲ study comparing cisplatin plus gemcitahion with cisplatin plus pemetrexed in chemotherapy.naive patients with advancedstage non-small cell lung cancer[J].J Clin Gncol,2008,(21):3543-3551.doi:10.1200/JCO.2007.15.0375.
  • 10廖日强,吴一龙.培美曲塞在肺癌治疗中的新进展[J].中国处方药,2010(3):46-49. 被引量:15

二级参考文献34

  • 1[1]Calvert H. An overview of folate metabolism: Features relevant to the action and toxicities of antifolate anticancer agents. Semin Oncol, 1999, 26 (2 Suppl 6) :3
  • 2[2]Sierra EE, Goldman ID. Recent advances in the understanding of the mechanism of membrane transport of folates and antifolates.Semin Oncol. 1999, 26 (2 Suppl 6): 11
  • 3[3]Mendelsohn LG, Shih C, Chen VJ, et al. Enzyme inhibition,polyglutamation, and the effect of LY231514 (MTA) on purine biosynthesis. Semin Oncol, 1999, 26 (2 Suppl 6):42
  • 4[4]Calvert H. MTA, a novel multitargeted antifolate, from preclinical to phase Ⅰ and beyond: Summary and conclusions. Semin Oncol, 1999, 26 (2 Suppl 6): 105
  • 5[5]Schultz RM, Chen VJ, Bewley JR, et al. Biological activity of the multitargeted antifolate, MTA (LY231514), in human cell lines with different resistance mechanisms to antifolate drugs. Semin Oncol, 1999, 26 (2 Suppl 6) :68
  • 6[6]Calvert AH, Walling JM. Clinical studies with MTA. Br J Cancer, 1998, 78 (Suppl 3) :35
  • 7[7]Newell DR. Clinical pharmacokinetics of antitumor antifolates.Semin Oncol, 1999, 26 (2 Suppl 6):74
  • 8[8]Thodtmann R, Depenbrock H, Dumez H, et al. Clinical and pharmacokinetic phase Ⅰ study of multitargeted antifolate (LY231514) in combination with cisplatin. J Clin Oncol,1999, 17 (10):3009
  • 9[9]Bajetta E, Celio L, Buzzoni R, et al. Phase Ⅱ study of pemetrexed disodium (Alimta) administered with oral folic acid in patients with advanced gastric cancer. Ann Oncol, 2003, 14(10): 1543
  • 10[10]Vogelzang NJ, Rusthoven JJ, Symanowski J, et al. Phase Ⅲstudy of pemetrexed in combination with cisplatin versus cisplatin alone in patients with malignant pleural mesothelioma. J Clin Oncol, 2003, 21 (14):2636

共引文献232

同被引文献76

引证文献11

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