解放军医学院学报
解放軍醫學院學報
해방군의학원학보
Academic Journal of Chinese Pla Medical School
2013年
10期
1013-1015,1035
,共4页
蓝玉玲%冯林春%蔡博宁%杨咏强%陈静
藍玉玲%馮林春%蔡博寧%楊詠彊%陳靜
람옥령%풍림춘%채박저%양영강%진정
放疗%食管癌%表皮生长因子受体%尼妥珠单克隆抗体
放療%食管癌%錶皮生長因子受體%尼妥珠單剋隆抗體
방료%식관암%표피생장인자수체%니타주단극륭항체
radiotherapy%esophageal cancer%epidermal growth factor receptor%nimotuzumab
目的:探讨放疗联合尼妥珠单抗治疗食管癌的近期疗效,生存率以及不良反应。方法回顾性分析我院2009-2012年经病理证实的34例食管鳞癌患者,其中根治性放疗24例,术后放疗10例,采用三维适形放疗(three dimensional conformal radiotherapy,3DCRT)或调强放射治疗(intensity madulated radiation therapy,IMRT),放疗剂量60~70 Gy,30~35次,5次/周。放疗同步联合尼妥珠单抗静脉滴注200 mg/次,1次/周,放疗前给药。采用RTOG/EROTC标准评价正常组织放射反应。结果根治性放疗组生存期满1年13例,2年5例,中位生存期15个月,近期疗效评价完全缓解(CR)8/24,部分缓解(PR)10/24,无缓解(NR)6/24,中位生存期分别为38个月,15个月,9个月(χ2=9.55,P=0.008)。术后放疗组生存期满1年6例,2年3例,平均生存期37个月。尼妥珠单抗联合放疗未引起过敏、皮疹、腹泻等药物反应。结论放疗联合尼妥珠单抗治疗食管癌安全有效。
目的:探討放療聯閤尼妥珠單抗治療食管癌的近期療效,生存率以及不良反應。方法迴顧性分析我院2009-2012年經病理證實的34例食管鱗癌患者,其中根治性放療24例,術後放療10例,採用三維適形放療(three dimensional conformal radiotherapy,3DCRT)或調彊放射治療(intensity madulated radiation therapy,IMRT),放療劑量60~70 Gy,30~35次,5次/週。放療同步聯閤尼妥珠單抗靜脈滴註200 mg/次,1次/週,放療前給藥。採用RTOG/EROTC標準評價正常組織放射反應。結果根治性放療組生存期滿1年13例,2年5例,中位生存期15箇月,近期療效評價完全緩解(CR)8/24,部分緩解(PR)10/24,無緩解(NR)6/24,中位生存期分彆為38箇月,15箇月,9箇月(χ2=9.55,P=0.008)。術後放療組生存期滿1年6例,2年3例,平均生存期37箇月。尼妥珠單抗聯閤放療未引起過敏、皮疹、腹瀉等藥物反應。結論放療聯閤尼妥珠單抗治療食管癌安全有效。
목적:탐토방료연합니타주단항치료식관암적근기료효,생존솔이급불량반응。방법회고성분석아원2009-2012년경병리증실적34례식관린암환자,기중근치성방료24례,술후방료10례,채용삼유괄형방료(three dimensional conformal radiotherapy,3DCRT)혹조강방사치료(intensity madulated radiation therapy,IMRT),방료제량60~70 Gy,30~35차,5차/주。방료동보연합니타주단항정맥적주200 mg/차,1차/주,방료전급약。채용RTOG/EROTC표준평개정상조직방사반응。결과근치성방료조생존기만1년13례,2년5례,중위생존기15개월,근기료효평개완전완해(CR)8/24,부분완해(PR)10/24,무완해(NR)6/24,중위생존기분별위38개월,15개월,9개월(χ2=9.55,P=0.008)。술후방료조생존기만1년6례,2년3례,평균생존기37개월。니타주단항연합방료미인기과민、피진、복사등약물반응。결론방료연합니타주단항치료식관암안전유효。
Objective To study the short-term curative effect, survival rate and adverse reactions in patients with esophageal cancer after radiotherapy combined with nimotuzumab. Methods The clinical data about 34 patients with pathology-confirmed esophageal squamous cancer admitted to our hospital from 2009 to 2012 were retrospectively analyzed. The patients were divided into radical radiotherapy group (n=24) and postoperative radiotherapy group (n=10). The patients received 3DCRT or IMRT at the dose of 60-70 Gy, 5 times a week for 30-35 times. Nimotuzumab was given by intravenous drip at the dose of 200 mg, once a week before radiotherapy. Radio-reactions of normal tissues were assessed according to the RTOG/EORTC criteria. Results Of the 24 patients in radical radiotherapy group, 13 survived 1 year and 5 survived 2 years with a mean survival time of 15 months. Short-term effect assessment showed that the curative, partial and no effect were achieved in 8, 10 and 6 out of the 24 patients, respectively, with mean survival time of 38, 15 and 9 months (χ2=9.55, P=0.008). Of the 10 patients in postoperative radiotherapy group, 6 survived 1 year and 3 survived 2 years with mean survival time of 37 months. No adverse reactions, such as allergic reaction, skin rush and diarrhea occurred after radiotherapy combined with nimotuzumab. Conclusion Radiotherapy combined with nimotuzumab is safe and effective modality for esophageal cancer.