期刊文献+

厄洛替尼治疗晚期非小细胞肺癌临床观察 被引量:4

The Evaluation of Advanced Non-small Cell Lung Cancer Treated with Erlotinib
下载PDF
导出
摘要 目的探讨厄洛替尼单药治疗晚期非小细胞肺癌(non-small cell lung cancer,NSCLC)的疗效和不良反应。方法 19例晚期NSCLC患者每天口服150 mg厄洛替尼治疗,直到肿瘤进展或因毒副作用不能耐受而终止治疗为止,评价其临床疗效、症状、生活质量、中位生存期、无疾病进展时间及毒副作用。结果 19例患者病灶总缓解率为26.32%,总控制率为73.68%,临床症状缓解率为78.95%。治疗有效患者治疗后血清癌胚抗原(carcinoem-bry-onic antigen,CEA)水平(16.91±24.95)μg.L-1较治疗前(53.18±38.46)μg.L-1明显降低,治疗后卡氏评分(karnofsky score,KPS)也明显提高(93.57±9.29 vs 57.14±15.90)。中位总生存期为11.4个月,无疾病进展时间11.1个月。不良反应主要为皮疹、腹泻,对症处理后均缓解。结论厄洛替尼治疗晚期NSCLC有一定的疗效,严重不良反应少。 Objective To observe the efficacy and toxicity of Erlotinib in the treatment of patients with advanced non-small cell lung cancer(NSCLC).Methods Nineteen patients with advanced NSCLC eat Erlotinib 150 mg per day.Until disease progression or ocwrrence of into lerable toxicity.Valuations were made for curative effects,symptoms,quality of life,mean survival time,time to progression-free and toxic reactions.Results Total mitigative rate of the focus was 26.32%,total control rate was 73.68%,all eviativerate of clinical symptoms was 78.95% and the levels of carcinoembryonic antigen(CEA) in the effective patients after treatment were significantly lower than those before the treatment(16.91±24.95 vs 53.18±38.46)μg·L-1.Meanwhile,kam of sky core(KPS) in the effective patients after treatment were obviously increased more than those before treatment(93.57±9.29 vs 57.14±15.90).Mean survival time of all the patients was 11.4 months.Time to progression-free was 11.1 months.The adverse reactions were mainly rash and diarrhea which could been released by treatments.Conclusion Erlotinib is effective and has fewer serious adverse reaction in treatment of patients with advanced NSCLC.
出处 《南昌大学学报(医学版)》 CAS 2010年第2期54-57,共4页 Journal of Nanchang University:Medical Sciences
基金 院级青年基金课题(YQN2009010)
关键词 厄洛替尼 非小细胞肺癌 分子靶向治疗 表皮生长因子受体 Erlotinib non-small cell lung cancer molecular targeting therapy epidermal growth factor receptor
  • 相关文献

参考文献5

二级参考文献18

  • 1陈智伟,廖美琳,陈玉蓉,赵家美,张心敏,成柏君.WHO标准和RECIST标准评价肺癌化疗疗效的比较[J].循证医学,2004,4(2):83-84. 被引量:33
  • 2廖秋林,李莲花,陈铭声.比较研究TPS、CEA、CYFRA21-1和STNFR四种肿瘤活性标志物在肺癌中的诊断价值[J].中国肺癌杂志,2005,8(4):309-312. 被引量:13
  • 3戚良晨,高楠,韩振国,马庆杰.肿瘤标志物联合检测在肺癌诊断中的价值[J].中国实验诊断学,2006,10(7):774-776. 被引量:17
  • 4SHEPHERD FA,PEREIRA JR,CIULEANU T,et al.Erlotinib in Previously Treated Non-Small-Cell Lung Cancer[J].N Engl J Med,2005,353(2):123-132
  • 5GATZEMEIER U,PLUZANSKA A.Results of a phase Ⅲ trial of erlotinib(OSI-774) combined with cisplatin and gemcitabine(GC)chemotherapy in advanced non-small cell lung cancer(NSCLC)[J].Proc Am Soc Clin Oncol,2004,22(14s):19s[Abstract 7010].
  • 6HERBST RS,PRAGER D.TRIBUTE-A phase Ⅲ trial of erlotinib HCl(OSI-774)combined with carboplatin and paclitaxel(CP)chemotherapy in advanced non-small cell lung cancer(NSCLC)[J].Proc Am Soc Clin Oncol,2004,22(14s):19s[Abstract 7011].
  • 7Salomon DS,Brandt R,Ciardiello F,et al.Epidermal growth factor-related peptides and their receptors in human malignancies[J].Crit Rev Oncol Hematot,1995,19:183-232.
  • 8Fontanini G,De Laurentiis M,Vignati S,et al.Evaluation of epidermal growth factor-related growth factors and receptors and of neoangiogenesis in completely resected stage Ⅰ-Ⅲ A non-small cell lung cancer:amphiregulin and microvessel count are independent prognostic indicators of survival[f].Clin Cancer Res,1998,4:241-249.
  • 9Grunwald V,Hidalgo M.Developing inhibitors of the epidermal growth factor receptor for cancer treatment[J].J Natl Cancer Inst,2003,95:851-867.
  • 10Shepherd FA,Rodrigues J,Ciuleanu T,et al.Erlotinib in previously treated non-small cell lung cancer[J].N Engl J Med,2005,353:123-132.

共引文献1547

同被引文献35

  • 1Socinski M A, Novello S, Brahmer J R, et al. Multicenter, phase II trial of sunitinib in previously treated, advanced nonsmall-cell lung cancer[J]. J Clin Oncol, 2008, 26(4): 650-656.
  • 2Gatzemeier U, Blumenschein G, Fosell F, et al. Phase Ⅱ trial of single-agent sorafenib in patients with advanced non-small cell lung carcinoma (abstract). J Clin Oncol 2006; 24:364s. (Abslract available online at www.asco.org/portal/site/ASCO/menuitem.34 d60f5624ba07fd506fe310ee37a01 d/?vgnextoid=76f8201 eb6 la7010VgnVCM100000ed730adlRCRD, accessed on June 7, 2006).
  • 3Scagliotti G, von Pawel J, Reck M, et al. Sorafenib plus carboplatin/paclitaxel in chemonaive patients with stage lIB-IV non-small cell lung cancer (NSCLC): Interim analysis results from the phase Ⅲ, randomized, double-blind, placebo-controlled, ESCAPE (Evaluation of Sorafenib, Carboplatin, And Paclitaxel Efficacy in NSCLC) trial[J]. J Thorac Oncol, 2008, 3: 687-673.
  • 4Schiller J H, Larson, T, Ou S I, et al. Efficacy and safety of axitinlb (AG-013736; AG) in patients (pts) with advanced non-small cell lung cancer (NSCLC): A phase Ⅱ trial. (Abstract). J Clin Oncol 2007; 25:386s. (Abstract available online at:www.asco.org/portal/ site/ASCO/menuitem.34d60f5624ba07fd506fe310ee37a01 d/?vg nextoid=76f8201 eb61 a7010VgnVCM 100000ed730ad 1RCRD, accessed on June 6, 2007).
  • 5Lilenbaum R, Socinski M A, Altorki N K, et al. Randomized phase Ⅱ trial of docetaxel/irinotecan and gemcitabine/ irinotecan with or without celecoxib in the second-line treatment of non-small-cell lung cancer[J]. J Clin Oncol, 2006, 24(30): 4825-4835.
  • 6Edelman M J, Watson D, Wang X, et al. Eicosanoid modulation in advanced lung cancer: cyclooxygenase-2 expression is a positive predictive factor for celecoxib +chemolherapy-Cancer and Leukemia Group B Trial 30203[J]. J Clin Oncol, 2008, 26(6): 848-855.
  • 7Leighl N B, Paz-Ares L, Douillard J Y, et al. Randomized phase Ⅲ study of matrix metalloproteinase inhibitor BMS-275291 in combination with paclitaxel and carboplatin in advanced non-smallcell lung cancer: National Cancer Institute of Canada-Clinical Trials Group Study BR. 18[J]. J Clin Oncol, 2005, 23(12): 2831-2839.
  • 8McKeage M. Phase Ib/Ⅱ study of DMXAA combined with carboplatin and paclitaxel in non-small cell lung cancer (abstract). J Clin Oncol 2006; 24:389s. (Abstract available online at www.asco.org/portal/site/ASCO/menuitem.34d60f5 624ba07fd506fe310ee37a01 d/?vgnextoid=76f8201 eb61 a7010 VgnVCM 100000ed730adl RCRD, accessed on June 29,2008).
  • 9Heinrich M C, Blanke C D, Druker B J, et al. Inhibition of KIT tyrosine kinase activity: A novel molecular approach to the treatment of KIT-positive malignancies[J]. J Clin Oncol 2002, 20(6): 1692-1673.
  • 10Langer C J, Stephenson P, Thor A, et al. Trastuzumab in the treatment of advanced non-small-cell lung cancer: is there a role? Focus on Eastern Cooperative Oncology Group study 2598[J]. J Clin Oncol, 2004, 22(7): 1180-1187.

引证文献4

二级引证文献15

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