期刊文献+

伊立替康联合顺铂治疗复发晚期小细胞肺癌29例 被引量:3

Curative effect of irinotecan combined with cisplatin treated for recrudescent advanced small cell lung cancer in 29 cases
下载PDF
导出
摘要 目的观察伊立替康(CPT-11)联合顺铂(DDP)治疗复发晚期小细胞肺癌的疗效及安全性。方法选择复发晚期小细胞肺癌患者29例,给予CPT-11 80 mg.m-2,静脉滴注,第1、8天;DDP 75 mg.m-2,静脉滴注,第2天至第5天;28 d为1个周期。化学治疗前常规给予抗呕吐治疗;化学治疗期间给予水化利尿及对症支持治疗。至少2个周期化学治疗后评价疗效。结果 29例中,完全缓解2例(6.9%),部分缓解9例(31.0%),稳定10例(34.5%),病情进展8例(27.6%),总有效率为37.9%。中位生存期7.4个月。主要不良反应:白细胞减少27例(93.1%),血小板减少15例(51.7%),恶心、呕吐19例(65.4%),迟发性腹泻19例(65.4%)。无毒性相关死亡病例。结论 CPT-11联合DDP二线治疗复发晚期小细胞肺癌有效率较高,毒副作用可以耐受。 Objective To evaluate the efficacy and safety of the irinotecan(CPT-11) combined with cisplatin(DDP) for recrudescent advanced small cell lung cancer(SCLC) patients.Methods 29 patients with recrudescent advanced SCLC were selected.The patients were treated with CPT-11 80 mg·m-2 on the first day and the eighth day by intravenous drip,and cisplatin 75 mg·m-2 from the second day to the fifth day by intravenous drip,a cycle was 28 days.Conventional treatment to against nausea and vomiting was given before chemotherapy;hydration diuresis and supporting therapy were given during the period of chemotherapy.Curative effect was evaluated after chemotherapy at least for two cycles.Results In 29 evaluable patients,response including 2(6.9%) cases were complete remissions and 9(31.0%) cases were partial remission,10(34.5%)patients had stable disease and 8(27.6%) had progressive disease,the total effective rate was 37.9%.The median survival time was 7.4 months.The main toxicity reaction was leucopenia(93.1%),thrombocytopenia(51.7%),nausea and vomiting(65.4%) and tardive diarrhea(65.4%).Non-toxic related death was found in the 29 cases.Conclusion The effective rate of irinotecan combined with cisplatin as second-line therapy treated for recrudescent advanced SCLC is highly active and the toxic reaction can be tolerated.
出处 《新乡医学院学报》 CAS 2012年第5期352-353,356,共3页 Journal of Xinxiang Medical University
关键词 伊立替康 顺铂 小细胞肺癌 irinotecan cisplatin small cell lung cancer
  • 相关文献

参考文献10

  • 1Ganti A K,West W W,Lackner R P,et al.Current concepts in thediagnosis and management of small-cell lung cancer[J].Oncology(Williston Park),2010,24(11):1034-1039.
  • 2王煜霞,王雷,常海敏.Topo-Ⅱ蛋白与p53蛋白在非小细胞肺癌耐药性中的表达[J].新乡医学院学报,2012,29(1):36-39. 被引量:4
  • 3徐艳,黄茂,丁惠珍.非小细胞肺癌患者化疗前后淋巴细胞亚群监测的临床意义[J].实用临床医药杂志,2011,15(19):31-33. 被引量:8
  • 4Simon M,Argiris A,Murren J R.Progress in the therapy of smallcell lung cancer[J].Crit Rev Oncol Hematol,2004,49(2):119-133.
  • 5Johnson B E,Janne P A.Basic treatment considerations usingchemotherapy for patients with small cell lung cancer[J].Hema-toloncol Clin North Am,2004,18(2):309-322.
  • 6孙艳,石远凯.临床肿瘤内科手册[M].5版.北京:人民卫生出版社,2007:54-56.
  • 7Agra Y,Pelayo M,Sacristan M,et al.Chemotherapy versus bestsupportive care for extensive small cell lung cancer[J].CochraneDatabase Syst Rev,2003(4):CD001990.
  • 8Noda K,Nishiwaki Y,Kawahara M,et al.Irinotecan plus cisplatincompared with etoposide plus cisplatin for extensive small cell lungcancer[J].N Engl J Med,2002,346(2):85-91.
  • 9Hermes A,Bergman B,Bremnes R,et al.Irinotecan plus carbopla-tin versus oral etoposide plus carboplatin in extensive small-celllung cancer:a randomized phase III trial[J].J Clin Oncol,2008,26(26):4261-4267.
  • 10田村友秀,钱冬梅.小细胞肺癌化疗的最新进展[J].日本医学介绍,2002,23(9):385-386. 被引量:5

二级参考文献20

共引文献14

同被引文献34

  • 1云径平,向锦,侯景辉,田秋红,符珈.CD56在小细胞癌组织中的表达及其对诊断的作用[J].癌症,2005,24(9):1140-1143. 被引量:26
  • 2Fujiwara Y, Minami H. An overview of the recent progress in irinotecan pharmacogenetics [ J ]. Pharmacogenomics, 2010,11(3) :391-406.
  • 3de Jong F A, Kehrer D F, Mathijssen R H, et al. Prophy- laxis of irinotecan-induced diarrhea with neomycin and po- tential role for UGT1AI" 28 genotype screening: a double- blind, randomized, placebo-controlled study[J]. Oncologist, 2006,11 (8) :944-954.
  • 4Innocenti F, Kroetz D L, Schuetz E, et al. Comprehensive pharmacogenetic analysis of irinotecan neutropenia and phar- maeokineties [ J J . J Clln Oneol , 2009,27(16):2604-2614.
  • 5Hahn K K, Wolff J J, Kolesar J M. Pharmacogenetics and irinotecan therapy [ J ]. Am J Health Syst Pharm, 2006,63 (22) :2211-2217.
  • 6Ando Y, Saka H, Ando M, et al. Polymorphisms of UDP- glucuronosyltransferase gene and irinotecan toxicity: aphar- macogenetic analysis [ J ]. Cancer Res, 2000,60 ( 24 ) : 6921- 6926.
  • 7Innocenti F, Undevia S D, lyer L, et al. Genetic variants in the UDP-glueuronosyltransferase 1A1 gene predict the risk of severeneutropenia of irinotecan [ J ]. J Clin Oncol, 2004,22 (8) :1382-1388.
  • 8Desai A A, Innocenti F, Ratain M J. Pharmacogenomies: road to anticancer therapeutics nirvana? [ J ]. Oncogene, 2003,22 ( 42 ) : 6621-6628.
  • 9Onoue M, Terada T, Kobayashi M, et al. UGT1A1 *6 poly- morphism is most predictive of severe neutropenia induced by irinotecan inJapanese cancer patients [ J ]. Int J Clin Oncol, 2009,14(2) :136-142.
  • 10Takano M, Kato M, Yoshikawa T, et al. Clinical signifi- cance of UDP-glucuronosyltransferase 1A1 *6 for toxicities of combination chemotherapy with irinoteean and cisplatin in gynecologic cancers: a prospective multi-institutional study [J]. Oncology, 2009,76(5) :315-321.

引证文献3

二级引证文献13

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