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作 者:林丹霞[1] 陈晨[2] 杨钰贤[1] 曾德[1] 吴晓[3] 林慧[1] 杜彩文[1]
机构地区:[1]汕头大学医学院附属肿瘤医院肿瘤内科,广东汕头515041 [2]汕头大学医学院附属肿瘤医院药剂科,广东汕头515041 [3]汕头大学医学院附属肿瘤医院病理科,广东汕头515041
出 处:《汕头大学医学院学报》2015年第2期106-107,共2页Journal of Shantou University Medical College
摘 要:目的:探讨培美曲塞或吉西他滨+顺铂治疗晚期肺腺癌的疗效和毒副作用。方法:64例晚期肺腺癌患者分为培美曲塞+顺铂(28例。培美曲塞500 mg/m2,第1 d,顺铂25 mg/m2,第1~3 d)和吉西他滨+顺铂(36例。吉西他滨1 000 mg/m2,第1d及第8 d,顺铂25 mg/m2,第1~3 d)组,治疗周期21 d。结果:培美曲塞、吉西他滨+顺铂组总有效率分别为32.1%和27.8%,中位无疾病进展时间6.7和6.3个月,中位生存期16.0和13.8个月。培美曲塞+顺铂组WBC减少、血小板降低明显低于吉西他滨+顺铂组(P〈0.05)。结论:培美曲塞+顺铂可作为初治晚期肺腺癌安全有效的药物。Objective:To explore the efficacy and side effects of pemetrexed or gemcitabine combined with cisplatin in the treatment of advanced lung adenocarcinoma. Methods:Sixty-four patients with advanced lung adenocarcinoma were divided into pemetrexed combined with cisplatin group(28 case. Pemetrexed 500 mg/m2 iv infusion d1,cisplatin 25 mg/m2 iv infusion d1~3)and gemcitabine combined with cisplatin group(36 cases. Gemcitabine 1 000 mg/m2 iv infusion d1,8,cisplatin 25 mg/m2 iv infusion d1~3). The treatment cycle was 21 days. Results:The total effective rate in the pemetrexed+cisplatin group was 32.1%,27.8% of gemcitabine+cisplatin group. The median progression free survival in the pemetrexed+cisplatin group was 6.7 months,6.3 months of gemcitabine+cisplatin group. The median survival time in the pemetrexed+cisplatin group was 16.0 months,13.8 months of gemcitabine+cisplatin group. The white blood cell reduction and lower platelet count in the pemetrexed+cisplatin group were significantly lower than those in the gemcitabine+cisplatin group(P0.05). Conclusion : Pemetrexed+cisplatin can be used as a safe and effective drug for advanced lung adenocarcinoma.
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