{"title":"Efficacy comparison of concurrent chemoradiotherapy with nedaplatin and cisplatin in inoperable locally-advanced non-small cell lung cancer","authors":"Yong-lin Wu, Kuantang Chen, Jun Wang","doi":"10.5428/PCAR20200508","DOIUrl":null,"url":null,"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.","PeriodicalId":19943,"journal":{"name":"药学服务与研究","volume":"20 1","pages":"355-376"},"PeriodicalIF":0.0000,"publicationDate":"2020-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"药学服务与研究","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.5428/PCAR20200508","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Health Professions","Score":null,"Total":0}
引用次数: 0
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.