肿瘤研究与临床
腫瘤研究與臨床
종류연구여림상
CANCER RESEARCH AND CLINIC
2014年
8期
514-517,522
,共5页
师颖瑞%王晖%杨敬儒%杨锫%欧阳淑玉%胡炳强%席许平%吴湘玮%朱苏雨
師穎瑞%王暉%楊敬儒%楊锫%歐暘淑玉%鬍炳彊%席許平%吳湘瑋%硃囌雨
사영서%왕휘%양경유%양부%구양숙옥%호병강%석허평%오상위%주소우
食管肿瘤%放疗疗法%尼妥珠单抗%不良反应%预后
食管腫瘤%放療療法%尼妥珠單抗%不良反應%預後
식관종류%방료요법%니타주단항%불량반응%예후
Esophageal carcinoma%Radiotherapy%Nimotuzumab%Side effects%Prognosis
目的 比较食管癌后程加速超分割调强适形放疗和后程加速超分割调强适形放疗联用尼妥珠单抗的疗效与毒性.方法 64例无远处转移的初治、评估认为无法耐受同步放化疗的食管鳞状细胞癌患者随机分组,32例行后程加速超分割调强适形放疗(后超调强组):先行放疗41.4 Gy/23次,共5周,后行放疗27 Gy/18次,共2周;32例行后程加速超分割调强适形联合尼妥珠单抗治疗(联合组):放射治疗方法同后超调强组,在放射治疗的开始时同期均加用6~8周的尼妥珠单抗(200 mg,静脉滴注,1次/周,共6~8周),从放疗第1天起执行.观察指标主要包括食管和肺的近期急性反应和后期放射损伤、过敏等不良反应以及临床受益率、1~3年局控率、无瘤生存率、总体生存率等.结果 后超调强组和联合组患者在放射性食管炎、放射性肺炎、骨髓抑制、消化道反应、皮疹、过敏等不良反应的发生方面差异无统计学意义(P>0.05).晚期并发症主要表现为食管狭窄和肺纤维化,两组比较差异无统计学意义(P>0.05).联合组有1例患者出现过敏性休克后放弃治疗.后超调强组和联合组患者临床受益率分别为75.0%(24/32)、93.7%(30/32),两组差异有统计学意义(P<0.05).联合组总生存率和无瘤生存率均高于后超调强组,但差异无统计学意义(P>0.05).结论 后程加速超分割调强适形放疗联合尼妥珠单抗治疗食管癌临床受益率明显高于后超调强组,但无瘤生存率和总体生存率的差别无统计学意义;后程加速超分割调强适形放疗联合尼妥珠单抗治疗食管癌未明显增加不良反应,部分可能出现过敏反应,应注意预防和加强处理.
目的 比較食管癌後程加速超分割調彊適形放療和後程加速超分割調彊適形放療聯用尼妥珠單抗的療效與毒性.方法 64例無遠處轉移的初治、評估認為無法耐受同步放化療的食管鱗狀細胞癌患者隨機分組,32例行後程加速超分割調彊適形放療(後超調彊組):先行放療41.4 Gy/23次,共5週,後行放療27 Gy/18次,共2週;32例行後程加速超分割調彊適形聯閤尼妥珠單抗治療(聯閤組):放射治療方法同後超調彊組,在放射治療的開始時同期均加用6~8週的尼妥珠單抗(200 mg,靜脈滴註,1次/週,共6~8週),從放療第1天起執行.觀察指標主要包括食管和肺的近期急性反應和後期放射損傷、過敏等不良反應以及臨床受益率、1~3年跼控率、無瘤生存率、總體生存率等.結果 後超調彊組和聯閤組患者在放射性食管炎、放射性肺炎、骨髓抑製、消化道反應、皮疹、過敏等不良反應的髮生方麵差異無統計學意義(P>0.05).晚期併髮癥主要錶現為食管狹窄和肺纖維化,兩組比較差異無統計學意義(P>0.05).聯閤組有1例患者齣現過敏性休剋後放棄治療.後超調彊組和聯閤組患者臨床受益率分彆為75.0%(24/32)、93.7%(30/32),兩組差異有統計學意義(P<0.05).聯閤組總生存率和無瘤生存率均高于後超調彊組,但差異無統計學意義(P>0.05).結論 後程加速超分割調彊適形放療聯閤尼妥珠單抗治療食管癌臨床受益率明顯高于後超調彊組,但無瘤生存率和總體生存率的差彆無統計學意義;後程加速超分割調彊適形放療聯閤尼妥珠單抗治療食管癌未明顯增加不良反應,部分可能齣現過敏反應,應註意預防和加彊處理.
목적 비교식관암후정가속초분할조강괄형방료화후정가속초분할조강괄형방료련용니타주단항적료효여독성.방법 64례무원처전이적초치、평고인위무법내수동보방화료적식관린상세포암환자수궤분조,32례행후정가속초분할조강괄형방료(후초조강조):선행방료41.4 Gy/23차,공5주,후행방료27 Gy/18차,공2주;32례행후정가속초분할조강괄형연합니타주단항치료(연합조):방사치료방법동후초조강조,재방사치료적개시시동기균가용6~8주적니타주단항(200 mg,정맥적주,1차/주,공6~8주),종방료제1천기집행.관찰지표주요포괄식관화폐적근기급성반응화후기방사손상、과민등불량반응이급림상수익솔、1~3년국공솔、무류생존솔、총체생존솔등.결과 후초조강조화연합조환자재방사성식관염、방사성폐염、골수억제、소화도반응、피진、과민등불량반응적발생방면차이무통계학의의(P>0.05).만기병발증주요표현위식관협착화폐섬유화,량조비교차이무통계학의의(P>0.05).연합조유1례환자출현과민성휴극후방기치료.후초조강조화연합조환자림상수익솔분별위75.0%(24/32)、93.7%(30/32),량조차이유통계학의의(P<0.05).연합조총생존솔화무류생존솔균고우후초조강조,단차이무통계학의의(P>0.05).결론 후정가속초분할조강괄형방료연합니타주단항치료식관암림상수익솔명현고우후초조강조,단무류생존솔화총체생존솔적차별무통계학의의;후정가속초분할조강괄형방료연합니타주단항치료식관암미명현증가불량반응,부분가능출현과민반응,응주의예방화가강처리.
Objective To compare the treatment result and the toxicity between the late course accelerated hyperfractionated intensity modulated radiation therapy (LCAF) and LCAF plus nimotuzumab for esophageal carcinoma.Methods 64 patients with esophageal squamous cell carcinoma without distance relapse and cannot tolerate the concurrent chemoradiotherapy were randomized into two groups.32 patients in group of LCAF received the first stage of radiation with a dose of 41.4 Gy/23 f/5 weeks,and then received the second stage of radiation with a dose of 27 Gy/18 f/2 weeks.32 patients in group of combination were treated by the same way plus nimotuzumab.The toxicity,the late reaction,the response rate,local control rate,distant-metastasis-free survivalrate and total survivalrate were compared between the two groups.Results The incidence of toxicity including radiation esophagitis,radiation pneumonitis,myelosuppression,gastrointestinal reaction,tetter and allergy showed no significant difference between group LCAF and group combination (P > 0.05).The incidence of late complications as esophagostenosis and lung fibrosis have no significance between group LCAF and group combination (P > 0.05).One patient in group of combination appeared anaphylactic shock and gave up the treatment.The response rate in group of combination was significant improved compared with group of LCAF (75.0 % vs 93.7 %,P < 0.05).The over survival rate and the distant-metastasis-fiee survival rate in group of combination were higher than those in group of LCAF,but showed no statistical significance (P > 0.05).Conclusions Most patients of esophageal carcinoma have good tolerance of LCAF plus nimotuzumab.Anaphylactic reaction maybe appear while accepting nimotuzumab which need be mentioned.The over survival rate and the distant-metastasis-free survival rate of LCAF plus nimotuzumab are advantage,but has no statistical significance,LCAF combined with nimotuzmab has a higher clinical benefit.