培美曲塞与吉西他滨联合顺铂一线治疗晚期非小细胞肺癌的对比研究

    Comparisive study between pemetrexed and gemcitabine combined with cisplatin in the treatment of advanced non-small cell lung cancer

    • 摘要: 目的:探讨培美曲塞与吉西他滨联合顺铂一线治疗晚期非小细胞肺癌(NSCLC)的临床疗效及不良反应。方法:分析晚期NSCLC一线化疗病人46例,采用培美曲塞联合顺铂化疗组22例(培美曲塞组),吉西他滨联合顺铂化疗组24例(吉西他滨组)。比较2组病人的近期疗效、中位无疾病进展生存时间(PFS)和不良反应发生情况。结果:培美曲塞组和吉西他滨组的客观缓解率分别为36.4%和29.2%,疾病控制率分别为62.5%和45.8%,中位PFS分别为6.5个月和6.0个月,差异均无统计学意义(P>0.05)。2组病人不良反应均可耐受。培美曲塞组和吉西他滨组粒细胞减少分别为36.4%(8/22)和66.7%(16/24),差异有统计学意义(P<0.05)。结论:培美曲塞或吉西他滨联合顺铂治疗晚期NSCLC的临床疗效相似,但前者不良反应发生率减低,病人耐受性较好,值得临床推广。

       

      Abstract: Objective:To explore the clinical efficacy and toxicity of pemetrexed or gemcitabine combined with cisplatin in the treatment of patients with advanced non-small cell lung cancer(NSCLC).Methods:Among 46 patients with advanced NSCLC,22 cases were treated with pemetrexed combined with cisplatin(pemetrexed group) and 24 cases were treated with gemcitabine combined with cisplatin(gemcitabine group).The short-term efficacy,median disease-free progression survival(PFS) time and adverse reactions between two groups were compared.Results:The objective remission rate,disease control rate and median PFS in pemetrexed group and gemcitabine group were(36.4% and 29.2%),(62.5% and 45.8%),and(6.5 and 6.0 months),respectively,and the differences of the objective remission rate,disease control rate and median PFS between two groups were not statistically significant(P>0.05).The adverse reactions in two groups were tolerable.The rates of neutrophil reduction in pemetrexed group and gemcitabine group were 36.4%(8/22) and 66.7%(16/24),respectively,and the difference of which between two groups was statistically significant(P<0.05).Conclusions:The clinical effect between pemetrexed combined with cisplatin and gemcitabine combined with cisplatin in the treatment of advanced NSCLC is similar,but the pemetrexed combined with cisplatin is less toxicities,good tolerability,worthy of application.

       

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