期刊文献+

3周重复改良FOLFIRI方案作为转移性大肠癌维持化疗的临床观察 被引量:1

下载PDF
导出
摘要 目的 观察3周重复改良FOLFIRI方案作为转移性大肠癌维持化疗的疗效和毒性。方法 21例转移性大肠癌患者,采用2周重复FOLFIRI方案一线治疗8~9个周期;疗效评价为无进展者采用3周重复改良FOLFIRI方案维持化疗,持续到疾病进展或出现不能耐受毒性为止。结果 全组经一线治疗后获CR 1例,PR 11例,SD 9例。维持化疗平均治疗6个周期,中位PFS为8.9个月,中位OS为20.9个月。主要毒副反应为恶心/呕吐、腹泻、白细胞下降和乏力等。结论 3周重复改良FOLFIRI方案可作为转移性大肠癌患者的维持化疗,能改善患者生活质量,毒副反应较轻。
出处 《中国癌症防治杂志》 CAS 2014年第3期295-297,共3页 CHINESE JOURNAL OF ONCOLOGY PREVENTION AND TREATMENT
  • 相关文献

参考文献11

  • 1詹丽芬,许慎,蔡友鹏,甘立菁.FOLFIRI方案一线治疗晚期大肠癌的临床观察[J].现代肿瘤医学,2012,20(3):568-570. 被引量:8
  • 2Labianca R,Sobrero A,Isa L,et al.Intermittent versus continuous chemotherapy in advanced colorectal cancer:a randomised 'GISCAD' trial[ J ].Ann Oncol, 2011,22(5) : 1236-1242.
  • 3Tournigand C,Andre T,Achille E, et al.FOLFIRI followed by FOL- FOX6 or the reverse sequence in advanced colorectal cancer: a ran- domized GERCOR study[J].J Clin 0ncol,2004,22(2):229-237.
  • 4Stintzing S, Fischer yon Weikersthal L, Decker T, et aI.FOLFIRI plus eetuximab versus FOLFIRI plus bevacizumab as first-line treatment for patients with metastatic colorectal cancer-subgroup analysis of patients with KRAS:mutated tumours in the randomised German AIO study KRK-0306[ J ].Ann Oncol, 2012,23(7 ) : 1693-1699.
  • 5Day RS.Treatment sequencing,asymmetry,and uncertainty:protocol atrategies for combination chemotherapy [ J ].Cancer Res, 1986,46 ( 8 ) : 3876-3885.
  • 6Tournigand C, Cervantes A, Figer A, et al.OPTIMOX1 : a randomised study of FOLFOX4 or FOLFOX7 with oxaliplatin in a stop-and-go fashion in advanced colorectal cancer-va GERCOR study[J].J Clin Oncol, 2006,24(3 ) : 394-400.
  • 7Chibaudel B,Maindrault-Goebel F,Lledo G,et al.Can chemotherapy be discontinued in unresectable metastatic colorectal cancer?The GERCOR OPTIMOX2 Study [ J ].J Clin Oncol, 2009,27 ( 34 ) : 5727- 5733.
  • 8Colueci G, Gebbia V, Paoletti G, et al.Phase III randomized trial of FOLFIRI versus FOLFOX4 in the treatment of advanced eolorectal eaneer:a multicenter study of the gruppo oncologico Dell' Italia meridionale[J].J Clin 0neol,2005,23(22):4866-4875.
  • 9Carrato A,Swieboda-Sadlej A,Staszewska-Skurczynska M,et al.Flu- orouracil,leucovorin, and irinotecan plus either sunitinib or placebo in metastatic colorectal cancer:a randomized,phase l]I trial[Jl.J Clin Oncol,2013,31(10) : 1341-1347.
  • 10Diaz-Rubio E,Gomez-Espana A,Massuti B,et al.First-line XELOX plus bevacizumab followed by XELOX plus bevacizumab or single- agent bevacizumab as maintenance therapy in patients with metastatic colorectal cancer: the phase III MACRO TTD study[J]. Oncologist, 2012,17( 1 ) : 15-25.

二级参考文献12

  • 1陈映霞,秦叔逵,王琳,何泽明,钱军,张珏,李慧.FOLFIRI治疗转移性大肠癌37例临床研究[J].中国肿瘤,2006,15(7):481-483. 被引量:4
  • 2Douillard JY,Sobrero A,CarnaghiC,et al.Metastatic colorectal cancer:integrating irinotecan in combination and sequential chem-otherapy[J].Ann Oncol,2003,14(Suppl2):7-12.
  • 3Saltz LB,Cox JV,Blanke C,et al.Irinotecan plus fluorouracil and leucovorin for metastatic colorectal cancer[J].N Engl J Med,2000,343(13):905-914.
  • 4Douillard JY,Cunningham D,Roth AD,et al.Irinotecan combined with fluorouracil compared with fluorouracil alone as first-line treatment for metastatic colorectal cancer:a multicentre randomised trial[J].Lancet,2000,355(9209):1041-1047.
  • 5Colucci G,Gebbia V,Paoletti G,et al.PhaseⅢrandomized trial of FOLFIRI versus FOLFOX4in the treatment of advanced colorectal cancer:a multicenter study of the Gruppo Oncologico Dell'Italia Me-ridionale[J].J Clin Oncol,2005,23(22):4811-4814.
  • 6Ando Y,Saka H,Ando M,et al.Polymorphisms of UDP-Glucuro-nosyl transferase gene and irinotecan toxicity:A pharmacogenetic a-nalysis[J].Cancer Res,2000,60(24):6921-6926.
  • 7Luis P,Eve P,Laura AC,et al.Utility of pretreatment bilirubin level and UGT1A1polymorphisms in multivariate predictive models of neutropenia associated with irinotecan treatment in previously un-treated patients with colorectal cancer[J].Arch Drug Inf,2008,1(3):97-106.
  • 8孙燕.肿瘤内科学[M].北京:人民卫生出版社,2001.450-451.
  • 9陈贵平,李德川.FOLFIRI治疗转移性结直肠癌34例临床观察[J].中国医院药学杂志,2008,28(8):640-642. 被引量:1
  • 10李琳,许崇安,刘艳,徐洁.FOLFIRI方案治疗晚期大肠癌32例临床观察[J].山东医药,2008,48(16):58-58. 被引量:1

共引文献7

同被引文献5

引证文献1

二级引证文献12

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