中华临床医师杂志(电子版)
中華臨床醫師雜誌(電子版)
중화림상의사잡지(전자판)
CHINESE JOURNAL OF CLINICIANS(ELECTRONIC VERSION)
2014年
8期
1423-1426
,共4页
朱眉%张洁%黄红霞%王萌萌%李润花%姚丽鸽%孔天东
硃眉%張潔%黃紅霞%王萌萌%李潤花%姚麗鴿%孔天東
주미%장길%황홍하%왕맹맹%리윤화%요려합%공천동
肺腺癌%培美曲塞%奈达铂%顺铂
肺腺癌%培美麯塞%奈達鉑%順鉑
폐선암%배미곡새%내체박%순박
Pulmonary adenocarcinoma%Pemetrexed%Nedaplatin%Cisplatin
目的:评价培美曲塞联合奈达铂在晚期肺腺癌一线化疗的疗效及不良反应。方法回顾性分析我院2008年6月至2013年6月收治的晚期肺腺癌72例,按纳入标准及用药方案,分为研究组和对照组,两组均给予培美曲塞500 mg/m2静脉滴注化疗,d1,研究组联合奈达铂80 mg/m2静脉滴注, d2,对照组予顺铂80 mg/m2静脉滴注化疗,d2,至少化疗2周期后评价疗效。结果研究组和对照组在近期疗效比较无统计学差异,ORR分别为51.5%和53.8%,DCR分别为63.6%和71.8%。不良反应比较,3~4级毒性研究组以中性粒细胞减少、血小板下降为主,对照组以恶心呕吐、肾功能异常为主,差异有统计学意义。结论培美曲赛联合奈达铂或者顺铂在晚期肺腺癌一线化疗疗效相似,但毒副反应各有不同,可根据患者不同情况选择合适的治疗方案。
目的:評價培美麯塞聯閤奈達鉑在晚期肺腺癌一線化療的療效及不良反應。方法迴顧性分析我院2008年6月至2013年6月收治的晚期肺腺癌72例,按納入標準及用藥方案,分為研究組和對照組,兩組均給予培美麯塞500 mg/m2靜脈滴註化療,d1,研究組聯閤奈達鉑80 mg/m2靜脈滴註, d2,對照組予順鉑80 mg/m2靜脈滴註化療,d2,至少化療2週期後評價療效。結果研究組和對照組在近期療效比較無統計學差異,ORR分彆為51.5%和53.8%,DCR分彆為63.6%和71.8%。不良反應比較,3~4級毒性研究組以中性粒細胞減少、血小闆下降為主,對照組以噁心嘔吐、腎功能異常為主,差異有統計學意義。結論培美麯賽聯閤奈達鉑或者順鉑在晚期肺腺癌一線化療療效相似,但毒副反應各有不同,可根據患者不同情況選擇閤適的治療方案。
목적:평개배미곡새연합내체박재만기폐선암일선화료적료효급불량반응。방법회고성분석아원2008년6월지2013년6월수치적만기폐선암72례,안납입표준급용약방안,분위연구조화대조조,량조균급여배미곡새500 mg/m2정맥적주화료,d1,연구조연합내체박80 mg/m2정맥적주, d2,대조조여순박80 mg/m2정맥적주화료,d2,지소화료2주기후평개료효。결과연구조화대조조재근기료효비교무통계학차이,ORR분별위51.5%화53.8%,DCR분별위63.6%화71.8%。불량반응비교,3~4급독성연구조이중성립세포감소、혈소판하강위주,대조조이악심구토、신공능이상위주,차이유통계학의의。결론배미곡새연합내체박혹자순박재만기폐선암일선화료료효상사,단독부반응각유불동,가근거환자불동정황선택합괄적치료방안。
Objective To evaluate the efficacy and adverse reactions of pemetrexed combined with nedaplatin or cisplatin in patients with advanced pulmonary adenocarcinoma. Methods From June 2008 to June 2013, 72 patients with pulmonary adenocarcinoma histopathology-confirmed were devided into the research group and the control group. The two groups were given pemetrexed with 500 mg/m2 intravenously, d1, nedaplatin was performed with 80 mg/m2 in the research group the next day, and cisplatin was performed with the same dose in the control group, the efficacy was evaluated after 2 cycles. Results For the nedaplatin group, objective response rate (ORR) was 51.5, disease control rate (DCR) was 63.6%, and In the cisplatin group, ORR was 53.8, DCR was 71.8%. There was no statistical significance (P>0.05). Furthermore, the most common toxicities in the nedaplatin group were neutropenia and thrombocytopenia, whereas those in the cisplatin group were nausea and vomiting, a normal renal function. Conclusion The efficacy was similar in the 2 groups, but the side effect was different, we can choose the appropriate individual patient treatment.