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伊立替康治疗宫颈癌的临床研究进展 被引量:3

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摘要 伊立替康(irinotecan,CPT-11)是喜树碱类衍生物,属拓扑异构酶I(Topo I)抑制剂,最早由日本研制开发,1987年开始I期临床实验,1998年获得美国FDA批准,用于标准化疗方案治疗失败后转移性结直肠癌的一线治疗.
出处 《肿瘤预防与治疗》 2010年第2期167-171,共5页 Journal of Cancer Control And Treatment
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参考文献25

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二级参考文献11

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共引文献23

同被引文献22

  • 1Siegel R, Ward E, Brawley O, et al. Cancer statistics, 2011 : the impact of eliminating socioeconomic and racial dispari- ties on premature cancer deaths [ J ]. CA Cancer J Clin, 2011,61 (42) :212.
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  • 3Park Sung Taek, Song Min Jong, Park Jong Sup. Incidence and clinicopathologic behavior of uterine cervical carcinoma in renal transplant recipients [ J ]. World Journal of Surgical Oncology,2011,9( 1 ) : 129.
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  • 7宋颖秋,伍钢,李贵玲,陈静,曹如波,尹中元,朱芳.盐酸伊立替康对局部晚期宫颈癌放射增敏的临床研究[J].临床肿瘤学杂志,2008,13(8):730-733. 被引量:5
  • 8毛晓敏,赵家菊,史元梅.盐酸伊立替康联合顺铂方案治疗宫颈癌21例毒副反应观察及护理[J].中国误诊学杂志,2008,8(32):7951-7952. 被引量:3
  • 9孙晓东,岳树香,李建伟.盐酸伊立替康临床应用研究进展[J].中国药业,2011,20(14):79-80. 被引量:14
  • 10陈克明,易村犍,易清华,魏华.宫颈癌术前使用伊立替康联合顺铂方案化疗的近期疗效观察[J].中华妇幼临床医学杂志(电子版),2011,7(4):290-291. 被引量:9

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