安徽医学
安徽醫學
안휘의학
ANHUI MEDICAL JOURNAL
2014年
9期
1223-1225
,共3页
江伟%张章%齐志峰%吴越菲%秦岭%刘鹏英%孙玲玲%王仪胜
江偉%張章%齊誌峰%吳越菲%秦嶺%劉鵬英%孫玲玲%王儀勝
강위%장장%제지봉%오월비%진령%류붕영%손령령%왕의성
非小细胞肺癌%化疗%靶向治疗%多西他赛
非小細胞肺癌%化療%靶嚮治療%多西他賽
비소세포폐암%화료%파향치료%다서타새
Non-small cell lung cancer%Chemotherapy%Target treatment%Docetaxel
目的:观察多西他赛联合铂类治疗晚期非小细胞肺癌( NSCLC )的临床疗效及不良反应。方法52例晚期NSCLC患者入组,16例为靶向治疗失败患者。多西他赛联合顺铂组( DP组)31例,多西他赛75 mg/m2,静脉滴注l h,第1 d;顺铂75 mg/m2,静脉滴注,分3 d平均给药。多西他赛联合卡铂组(DC组)21例,多西他赛75 mg/m2,静脉滴注l h,第1 d;卡铂AUC=5(300~400 mg/m2)计算,静脉滴注,第1 d。21~28 d为1个周期,化疗2个周期后评价疗效及不良反应。结果 DP组客观有效率(ORR)为38.7%,疾病控制率(DCR)为67.7%;DC组ORR为33.3%,DCR为61.9%,两组差异无统计学意义(P>0.05)。16例靶向治疗失败患者ORR为12.5%,DCR为50.0%。不良反应主要为骨髓抑制、恶心、呕吐和脱发。结论多西他赛联合铂类治疗晚期NSCLC疗效确切,不良反应可耐受。
目的:觀察多西他賽聯閤鉑類治療晚期非小細胞肺癌( NSCLC )的臨床療效及不良反應。方法52例晚期NSCLC患者入組,16例為靶嚮治療失敗患者。多西他賽聯閤順鉑組( DP組)31例,多西他賽75 mg/m2,靜脈滴註l h,第1 d;順鉑75 mg/m2,靜脈滴註,分3 d平均給藥。多西他賽聯閤卡鉑組(DC組)21例,多西他賽75 mg/m2,靜脈滴註l h,第1 d;卡鉑AUC=5(300~400 mg/m2)計算,靜脈滴註,第1 d。21~28 d為1箇週期,化療2箇週期後評價療效及不良反應。結果 DP組客觀有效率(ORR)為38.7%,疾病控製率(DCR)為67.7%;DC組ORR為33.3%,DCR為61.9%,兩組差異無統計學意義(P>0.05)。16例靶嚮治療失敗患者ORR為12.5%,DCR為50.0%。不良反應主要為骨髓抑製、噁心、嘔吐和脫髮。結論多西他賽聯閤鉑類治療晚期NSCLC療效確切,不良反應可耐受。
목적:관찰다서타새연합박류치료만기비소세포폐암( NSCLC )적림상료효급불량반응。방법52례만기NSCLC환자입조,16례위파향치료실패환자。다서타새연합순박조( DP조)31례,다서타새75 mg/m2,정맥적주l h,제1 d;순박75 mg/m2,정맥적주,분3 d평균급약。다서타새연합잡박조(DC조)21례,다서타새75 mg/m2,정맥적주l h,제1 d;잡박AUC=5(300~400 mg/m2)계산,정맥적주,제1 d。21~28 d위1개주기,화료2개주기후평개료효급불량반응。결과 DP조객관유효솔(ORR)위38.7%,질병공제솔(DCR)위67.7%;DC조ORR위33.3%,DCR위61.9%,량조차이무통계학의의(P>0.05)。16례파향치료실패환자ORR위12.5%,DCR위50.0%。불량반응주요위골수억제、악심、구토화탈발。결론다서타새연합박류치료만기NSCLC료효학절,불량반응가내수。
Objective To observe the efficacy and toxicities of docetaxel combined with platinum in the treatment of patients with advanced non-small cell lung cancer ( NSCLC) .Methods Fifty-two patients with advanced NSCLC were enrolled into the study ,of which 16 patients were failure of target treatment .Thirty-one patients received docetaxel plus cisplatin ,docetaxel 75 mg/m2 ,1-hour intravenous infusion d 1;cisplatin 75 mg/m2 , intravenous infusion , d 1 ~3 individually .Twenty-one patients received docetaxel plus carbeplatin , docetaxel 75 mg/m2,1-hour intravenous infusion d1;carboplatin ACU=5(300~400 mg/m2),intravenous infusion d1,the chemotherapy was repeated ev-ery 21~28 days,and the efficacy and toxicities were assessed after two cycles .Results The response rate was 38.7%,and disease control rate was 67.7%in the DP group;the response rate was 33.3%,and disease control rate was 61.9%in the DC group.The difference between the two groups had no statistical significance .The response rate was 12.5%,and disease control rate was 50.0%in the 16 patients who were failure of target treatment.The major toxicities included myelesuppression ,nausea,vomiting and alopecia.Conclusion The combined chemo-therapy of docetaxel with platinum is effective in the treatment of patients with advanced non -small cell lung cancer ,and the toxicities are tol-erable.