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长春瑞滨联合顺铂(NP)治疗晚期非小细胞肺癌的疗效及生存因素分析 被引量:1

Efficacy and analysis of survival associated factors of navelbine and cisplatin chemotheraphy on advanced non-small-cell lung cancer
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摘要 目的分析长春瑞滨(NVB)联合顺铂治疗晚期非小细胞肺癌(NSCLC)患者的临床疗效及预后相关性生存因素。方法 59例经病理或细胞学证实的Ⅲb~Ⅳ期晚期NSCLC患者均接受长春瑞滨联合顺铂(NP)治疗方案,服药前及服药后每2~3周进行疗效及全身评估。结果 59例NSCLC患者完全缓解6例(10.17%)、部分缓解17例(28.81%)、稳定19例(32.20%)、进展18例(30.51%),总有效率38.98%。中位总生存期14.9个月,无治疗相关性死亡。结论长春瑞滨(NVB)联合顺铂对晚期非小细胞肺癌有较好临床疗效,和患者的预后相关性生存因素密切相关。因此,长春瑞滨(NVB)联合顺铂可作为晚期NSCLC的较有效治疗方案。 Objective To evaluate the efficacy of navelbine and cisplatin chemotherapy on advanced non-small-cell lung cancer and analyze survival associated factors.Methods A total of 59 cases of stage Ⅲb~ⅣNSCLC confirmed by pathological and cytological examination were treated by chemotherapy of navelbine and cisplatin.Efficacy and whole body condition were evaluated before and every 2~3 weeks after administration of erlotinib.Results In 59 patients with NSCLC,6 cases(10.17%)were complete remission,17 cases(28.81%) partly remission,19 cases(32.20%)stable,and 18 cases(30.51%)progressed.The total effective rate was 38.98%.The median survival time was 14.9 months.There were no treatment-related deaths.Conclusion The chemotherapy of navelbine and cisplatin for advanced non-small-cell lung cancer has good clinical effect,and is closely related to survival factors of the prognosis of patients.Therefore,the chemotherapy of navelbine and cisplatin can be considered as an effective treatment for advanced-stage NSCLC.
作者 宣瑞萍 章俊
出处 《成都医学院学报》 CAS 2011年第1期61-62,共2页 Journal of Chengdu Medical College
关键词 长春瑞滨 顺铂 非小细胞肺癌 生存因素 navelbine cisplatin non-small-cell lung cancer survival associated factors
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  • 1段家华,王志刚.国产多西紫杉醇联合顺铂治疗晚期非小细胞肺癌的临床研究[J].中华肿瘤防治杂志,2006,13(17):1333-1335. 被引量:23
  • 2SocinskiMA, Morris DE, Masters GA, et al. Chemotherapeuticmanagement of stage Ⅳ non -small cell lung cancer[J]. Chest, 2003,123 ( 1 ) : 226 - 243.
  • 3Cats A. New development s in systemic clemot herapy in advancedcolorectal cancer [ J ]. Scand J Gast roenterol Suppl, 2003, 38 (239) : 78 - 86.
  • 4Jamieson SM, Liu J, Hsu T, et al. Paclitaxel induces nucleolarenlargement in dorsal root ganglion neurons in vivo reducing ox2aliplatin toxicity[J]. Br J Cancer,2003,88 (12) : 1 942 - 1 947.
  • 5Jansen B, Zangemeister-Wittke U. Antisense therapy for cancer-the time of truth. Lancet Oncol,2002,3(11) : 672-683.
  • 6Liekens S, De Clercq E, Neyts J. Angiogenesis: regulators and clinical applications. Biochem Pharmacol, 2001,61 ( 3 ): 253-270.
  • 7Fukuoka M, Yano S, Giaccone G, et al. Multi-institutional randomized phase Ⅱ trial of gefitinib for previously treated patients with advanced non-small-cell lung cancer. J Clin Oncol, 2003,21(12): 2237-2246.
  • 8Giaccone G, Herbst RS, Manegold C, et al. Gefitinib in combination with gemcitahine and cisplatin in advanced non-small-cell lung cancer: a phase Ⅲ trial -INTACT 1. J Clin Oncol. 2004 Mar 1;22(5): 777-784.
  • 9Herbst RS, Giaccone G, Schiller JH, et al. Gefitinib in combination with paclitaxel and carboplatin in advanced non-small-cell lung cancer: a phase Ⅲ trial-INTACT 2. J Clin Oncol,2004,22(5):785-794.
  • 10Falardeau P, Champagne P, Poyet P, et al. Neovastat, a naturally occurring multifunctional antiangiogenic drug, in phase Ⅲ clinical trials. Semin Oncol,2001,28(6): 620-625.

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