国际医药卫生导报
國際醫藥衛生導報
국제의약위생도보
INTERNATIONAL MEDICINE & HEALTH GUIDANCE NEWS
2012年
22期
3312-3315
,共4页
赵鹏%陈炳光%莫如康%刘图强%严明基
趙鵬%陳炳光%莫如康%劉圖彊%嚴明基
조붕%진병광%막여강%류도강%엄명기
晚期胃癌%HER-2%曲妥珠单抗%卡培他滨%顺铂
晚期胃癌%HER-2%麯妥珠單抗%卡培他濱%順鉑
만기위암%HER-2%곡타주단항%잡배타빈%순박
Advanced gastric cancer%HER-2%Trastuzumab%Capecitabine%Cisplatin
目的 探讨曲妥珠单抗联合卡培他滨和顺铂治疗HER2阳性晚期胃癌的临床疗效及安全性.方法 经病理组织学确诊为晚期胃癌或胃食管连接部腺癌,经免疫组化(IHC)和/或荧光原位杂交法(FISH)检测HER2阳性共30例,其中观察组14例,对照组(单用顺铂+卡培他滨方案)16例.观察组卡培他滨1000 mg/m2,bid,d1~14,q3w;顺铂40 mg/m2,d1 ~2,q3w,6周期,曲妥珠单抗首8 mg/kg,q3w,此后每周6mg/kg,q3w维持进展后停药;对照组单纯化疗6周期,观察其临床疗效与不良反应.结果 观察组总有效率为50.0%,中位存活期为12.8个月,中位TTP8.2月;对照组总有效率为37.5%,中位存活期为9.2个月,中位TTP5.6月,观察组总有效率及中位生存时间明显优于对照组(P<0.05);两组患者毒副反应轻重程度及发生率比较差异无显著性(P>0.05).结论 曲妥珠单抗联合化疗可提高HER-2阳性晚期胃癌治疗的临床疗效,安全可靠,可考虑做为选择方案之一.
目的 探討麯妥珠單抗聯閤卡培他濱和順鉑治療HER2暘性晚期胃癌的臨床療效及安全性.方法 經病理組織學確診為晚期胃癌或胃食管連接部腺癌,經免疫組化(IHC)和/或熒光原位雜交法(FISH)檢測HER2暘性共30例,其中觀察組14例,對照組(單用順鉑+卡培他濱方案)16例.觀察組卡培他濱1000 mg/m2,bid,d1~14,q3w;順鉑40 mg/m2,d1 ~2,q3w,6週期,麯妥珠單抗首8 mg/kg,q3w,此後每週6mg/kg,q3w維持進展後停藥;對照組單純化療6週期,觀察其臨床療效與不良反應.結果 觀察組總有效率為50.0%,中位存活期為12.8箇月,中位TTP8.2月;對照組總有效率為37.5%,中位存活期為9.2箇月,中位TTP5.6月,觀察組總有效率及中位生存時間明顯優于對照組(P<0.05);兩組患者毒副反應輕重程度及髮生率比較差異無顯著性(P>0.05).結論 麯妥珠單抗聯閤化療可提高HER-2暘性晚期胃癌治療的臨床療效,安全可靠,可攷慮做為選擇方案之一.
목적 탐토곡타주단항연합잡배타빈화순박치료HER2양성만기위암적림상료효급안전성.방법 경병리조직학학진위만기위암혹위식관련접부선암,경면역조화(IHC)화/혹형광원위잡교법(FISH)검측HER2양성공30례,기중관찰조14례,대조조(단용순박+잡배타빈방안)16례.관찰조잡배타빈1000 mg/m2,bid,d1~14,q3w;순박40 mg/m2,d1 ~2,q3w,6주기,곡타주단항수8 mg/kg,q3w,차후매주6mg/kg,q3w유지진전후정약;대조조단순화료6주기,관찰기림상료효여불량반응.결과 관찰조총유효솔위50.0%,중위존활기위12.8개월,중위TTP8.2월;대조조총유효솔위37.5%,중위존활기위9.2개월,중위TTP5.6월,관찰조총유효솔급중위생존시간명현우우대조조(P<0.05);량조환자독부반응경중정도급발생솔비교차이무현저성(P>0.05).결론 곡타주단항연합화료가제고HER-2양성만기위암치료적림상료효,안전가고,가고필주위선택방안지일.
Objective To investigate the clinical efficacy and safety of trastuzumab combined with capecitabine and cisplatin on the treatment of HER-2 positive advanced gastric cancer.Methods 30 cases were diagnosed as advanced gastric cancer or EGJ adenocarcinoma in histopathology or with HER2 positive gastric cancer by IHC and/or FISH.They were divided into the observation group(14 cases)and the control group(16 cases)(treated solely with cisplatin and capecitabine).The observation group was treated with capecitabine in 1000 mg/m2,bid,dl-14,q3w;cisplatin in 40 mg/m2,dl-2,q3w for six cycles.Furthermore,they were treated with trastuzumab in 8 mg/kg,q3w,and then in 6 mg/kg,q3w each week until continual improvement.The control group was treated solely with chemotherapy for six cycles.The clinical efficacy and toxic and adverse effects of both groups were observed.Results The ORR of the observation group was 50.0%,the median survival time was 12.8 months,and the median was TFP8.2 months.The ORR of the control group was 37.5%,the median survival time was 9.2 months,and the median was TTP5.6 months.The ORR and median survival time of the observation group were both significantly better than those of the control group(P< 0.05).There was no significant difference between both groups in toxic and adverse effects and the incidence(P > 0.05).Conclusions Together with chemotherapy,trastuzumab combination can improve the clinical efficacy of HER-2 positive advanced gastric cancer with safety and reliability.So now it serves as one of the alternative treatment options.