Efficacy comparison of concurrent chemoradiotherapy with nedaplatin and cisplatin in inoperable locally-advanced non-small cell lung cancer

Q4 Health Professions
Yong-lin Wu, Kuantang Chen, Jun Wang
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Abstract

Objective: To compare the efficacy and safety of concurrent chemoradiotherapy with nedaplatin and cisplatin in inoperative locally-advanced non-small cell lung cancer(NSCLC).Methods: Eighty patients with locally-advanced NSCLC treated in Guanyun County People’s Hospital,Lianyungang,Jiangsu Province,from January 2015 to January 2019 were enrolled as study subjects,and were randomly divided into the nedaplatin group and the cisplatin group,each consisting of 40 patients.The patients in the 2 groups were treated with linear accelerator 6 MV high energy X-ray and 3D-CRT,5 times a week for a succession of 6 weeks,with a total dosage of 55-66 Gy.Then,the patients were given paclitaxel(155 mg/m2) intravenously for 3 hours in the first day after radiotherapy,and the patients in the cisplatin group were treated with cisplatin(80 mg/m2) intravenously for 3 to 4 days,and the patients in the nedaplatin group were given nedaplatin(80 mg/m2) intravenously also for 3 to 4 days.The efficacy,the levels of such serum tumor markers as carcinoembryonic antigen(CEA),carbohydrate antigen 125(CA125),neuron specific enolase(NSE) and cytokeratin fragment antigen 21-1(CYFRA21-1),as well as the rate of adverse drug reactions(ADRs) were compared between the 2 groups.Results: There was no statistical significance in remission rate and disease control rate,when comparisons were made between the 2 groups(P>0.05).After treatment,CEA,CA125,NSE and CYFRA21-1 levels in the 2 groups were significantly lower than those before treatment(P<0.05).There were no significant differences in CEA and CA125 levels,when comparisons were made between the 2 groups(P>0.05).However,NSE and CYFRA21-1 levels in the patients of the nedaplatin group were significantly lower than those of the cisplatin group(P<0.05).The rates of leucopenia,neutropenia,nausea and vomiting,constipation or diarrhea,increase of blood urea nitrogen or creatinine,and weight loss in the nedaplatin group were significantly lower than those in the cisplatin group(P<0.05).Conclusion: Nedaplatin has similar efficacy as cisplatin in the treatment of inoperable locally-advanced NSCLC,with higher safety,meanwhile it could decrease the levels of NSE and CYFRA21-1.For this reason,it is worthy further clinical promotion.
奈达铂与顺铂同步放化疗治疗不能手术的局部晚期非小细胞肺癌疗效比较
目的:比较奈达铂与顺铂同步放化疗治疗非手术期局部晚期非小细胞肺癌(NSCLC)的疗效和安全性。方法:选取2015年1月至2019年1月在江苏省连云港市关云县人民医院接受治疗的80例局部晚期NSCLC患者作为研究对象,随机分为奈达铂组和顺铂组,每组40例。两组患者均采用直线加速器6 MV高能x射线+ 3D-CRT治疗,每周5次,连续6周,总剂量55 ~ 66 Gy。放疗后第1天给予紫杉醇(155 mg/m2)静脉滴注3小时,顺铂组给予顺铂(80 mg/m2)静脉滴注3 ~ 4天,奈达铂组给予奈达铂(80 mg/m2)静脉滴注3 ~ 4天。比较两组患者的疗效、血清肿瘤标志物癌胚抗原(CEA)、碳水化合物抗原125(CA125)、神经元特异性烯醇化酶(NSE)、细胞角蛋白片段抗原21-1(CYFRA21-1)水平及药物不良反应(adr)发生率。结果:两组患者缓解率、疾病控制率比较,差异均无统计学意义(P < 0.05)。治疗后,两组患者CEA、CA125、NSE、CYFRA21-1水平均显著低于治疗前(P0.05)。但奈达铂组患者NSE和CYFRA21-1水平显著低于顺铂组(P<0.05)。奈达铂组患者白细胞减少、中性粒细胞减少、恶心呕吐、便秘或腹泻、血尿素氮或肌酐升高、体重减轻率均显著低于顺铂组(P<0.05)。结论:奈达铂治疗不能手术的局部晚期NSCLC疗效与顺铂相似,安全性更高,同时可降低NSE和CYFRA21-1水平。因此,值得进一步临床推广。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
药学服务与研究
药学服务与研究 Health Professions-Pharmacy
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