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作 者:高建飞[1] 赵勇[1] 章必成[1] 朱宇泽[1] 饶智国[1] 刘健[1] 余丽芳[1] 杜光祖[1]
出 处:《临床肿瘤学杂志》2009年第8期698-700,共3页Chinese Clinical Oncology
摘 要:目的:比较紫杉醇脂质体(LEP)联合顺铂(DDP)组成的LP方案与紫杉醇(TAX)联合DDP组成的TP方案治疗晚期非小细胞肺癌(NSCLC)的疗效和毒副反应。方法:将89例晚期NSCLC患者随机分为LP组(57例)和TP组(32例),观察各组的近期及远期疗效、毒副反应和生存情况。结果:LP组和TP组的有效率分别为40.00%和38.71%,无显著性差异(P>0.05)。两组的肿瘤进展时间(TTP)分别为18周和17周,中位缓解期分别为20周和18周,中位生存期分别为35周和31周,1年生存率分别为35.09%和28.15%,均无显著性差异(P>0.05)。两组Ⅰ~Ⅱ度末梢神经炎发生率分别为19.29%和37.50%(P<0.05);Ⅰ~Ⅱ度过敏反应发生率分别为5.26%和12.50%(P<0.05);Ⅲ~Ⅳ度恶心呕吐发生率分别为5.26%和15.63%(P<0.01)。结论:LP与TP方案治疗晚期NSCLC疗效相似,但LP方案的外周神经毒性、过敏反应和恶心呕吐等毒副反应明显较低。LP方案可以作为晚期NSCLC的一线化疗方案。Objective:To evaluate the response and toxicity of liposome encapsulated paclitaxel(LEP) plus cisplatin(DDP)(LP regimen) and paclitaxel(TAX) plus DDP(TP regimen) in the treatment of advanced non-small cell lung cancer(NSCLC).Methods:A total of 89 cases with advanced NSCLC were randomized into two groups: LP group(57 patients) and TP group(32 patients).The response,toxicity and survival time of the two groups were compared.Results:The response rates were 40.00% and 38.71% in the LP and TP group respectively, but no significant difference was detected between them(P 〉0. 05). The median time to progression(ITP), median remission time, median survival time and 1 year survival rates were 18 weeks, 20 weeks, 35 weeks and 35.09% in LP group, and 17 weeks, 18 weeks, 31 weeks and 28. 15% in TP group, and no significant differences were detected between them( P 〉 0. 05 ). The grade Ⅰ-Ⅱ peripheral neuritis in TP group(37. 50% ) were higher than that in LP group( 19. 29% ) significantly(P 〈0. 05). The grade Ⅰ-Ⅱallergic reaction in TP group( 12. 50% ) was higher than that in LP group( 5.26% ) significantly( P 〈 0. 05 ). The grade Ⅲ-Ⅳnausea/vomiting in TP group( 15.63 % ) was higher than that in LP group (5, 26% ) significantly (P 〈 0. 01 ), too. Conclusion:The effect of LP regimen is similar to TP regimen, but peripheral neuritis, allergic reaction and nausea/vomiting in LP regimen are lower than those in TP regimen. In short, LP regimen may be the first line chemotherapy regimen of advanced NSCLC.
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