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大剂量法乐通加EP方案治疗耐药晚期非小细胞肺癌临床分析 被引量:2

High-dose toremifene plus EP regimen in the treatment of refractory advanced non-small cell lung cancer
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摘要 目的 评价大剂量法乐通加EP方案治疗难治性晚期非小细胞肺癌的疗效和毒副反应。方法 既往对含顺铂为主的化疗方案耐药的晚期非小细胞肺癌采用大剂量的法乐通加EP方案治疗 ,法乐通 4 80mg ,口服 ,连用 7.5d ;鬼臼乙叉甙 10 0mg m2 ,静滴 ,第 4~ 6天 ;顺铂 80mg m2 ,静滴 ,第 4天 ,每 4周重复。结果 共 5 0例进入临床研究 ,可评价疗效 4 3例 ,1例完全缓解 ,8例部分缓解 ,总有效率为 2 0 .9% (按ITT计算为 18.0 % ) ;中位生存期和无疾病进展生存期分别为 8.1和 3.2个月 ;1年生存率为 37.2 %。主要的不良反应为轻至中度的骨髓抑制、恶心和呕吐。结论 大剂量法乐通加EP方案治疗对铂类为主的化疗方案耐药的晚期非小细胞肺癌效果较好 ,不良反应轻 ,耐受性好。 Objective To evaluate the efficacy and safety of high-dose toremifene plus EP regimen in the treatment of refractory advanced non-small cell lung cancer (NSCLC).Methods The patients with previously DDP-resistant advanced NSCLC were treated with high-dose toremifene (480 mg,po,d1-7.5)plus EP regimen C (Vp-16 100 mg/m2 iv d4-6,DDP 80 mg/m2 iv d4) every 4 weeks.Results A total of 50 cases with advanced NSCLC resistant to DDP were enrolled,and 43 cases were valuable for efficacy assessment.One patient reached complete response (CR),8 reached partial response (PR),and the overall response rate was 20.9% (with ITT equal to 18.0%).The median survival time and the median progression-free survival time was 8.1 and 3.2 months respectively and 1-year survival rate was 37.2%.The major adverse effects were mild myelosuppression,nause and vomiting.Conclusions The high-dose toremifene plus EP regimen is effective in the treatment of advanced NSCLC resistant to DDP,and the adverse effects were tolerable.
出处 《中国肿瘤临床与康复》 2004年第6期531-533,共3页 Chinese Journal of Clinical Oncology and Rehabilitation
关键词 肺肿瘤/化学疗法 顺铂 法乐通 Lung neoplasms/chemotherapy Cisplatin Toremifene
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参考文献10

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共引文献6

同被引文献13

  • 1[1]Liippo K,Ellmen J,Vanttinen E,et al.Tore mifene concentration and multidrug resistance in lung tumors.Cancer Chemother Pharmacol,1997,39(3):212-216
  • 2Liippo K,Ellmen J,Vanttinen E,et al.Toremifene concentration and multidrug resistance in lung tumors [J].Cancer chemother Pharmacol,1997,39(3):212-216.
  • 3Chevalier T L,Brisgand D,Douillard J Y,et al.A randomized study of vinorelbine and cisplatin versus vindesine and cisplatin versus vinorelbine alone in advanced non-small cell lung cancer:results of a European multi-center trial including 612 patients[J].Clin Onco1,1994,12(2):360-367.
  • 4Schiller J H,Harrington D,Sandler A,et al.A randomized phase Ⅲ trial of four chemotherapy regimens in advanced nonsmall cell lung cancer [J].N Engl J Med,2002,346:92-98.
  • 5Fossella F V,Rigas J.The use of docetaxel (Taxotere) in patients with advanced non-small cell lung cancer previously treated with platinum-containing chemotherapy regimens[J].Semi On col,1999,26(3,Suppl Ⅱ):2-9.
  • 6Lara P Jr,Gandara D R,Gumerlocr P H,et al.Activity of high-dose toremifene plus cisplatin in platinum-treated nonsmall-cell-lung cancer:a phase of Ⅱ California Cancer Consortium Trial [J].Cancer Chemother Pharmacol,2001,48:22-28.
  • 7Fung H,Quinlan T R,Janssen Y M,et al.Inhibition of protein kinase C prevents asbestos-induced C-fos and C-Jun Proto-oncogene expression in mesothelial cells [J].Cancer Res,1997,57(15):3101-3104.
  • 8Berman E,Adam M,Duigou-osterndorf R,et al.Effect of tamoxifen on cell line displaying multidrug resistant phenotype[J].Blood,1991,77(4):818-825.
  • 9Stuart N S,Philip P,Horris A L,et al.High-dose tamoxifen as an enhancer of etoposide cytotoxicity,clinical effects and in vitro assess ment in P-gly-coprotein[J].Br J Cancer,1992,66:833-838.
  • 10Lara P Jr,Gandara D R,Wurz G T,et al.High-dose toremifene as a cisplatin modulator in metastatic non-small cell lung cancer:targeted plasma levels are achievable clinically [J].Cancer Che mother Pharmacol,1998,42 (6):504-508.

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