中华放射肿瘤学杂志
中華放射腫瘤學雜誌
중화방사종류학잡지
CHINESE JOURNAL OF RADIATION ONCOLOGY
2012年
6期
518-521
,共4页
贺春语%卜珊珊%张景伟%刘劲松%王雯%高华%陈永顺%吴小源%王建华
賀春語%蔔珊珊%張景偉%劉勁鬆%王雯%高華%陳永順%吳小源%王建華
하춘어%복산산%장경위%류경송%왕문%고화%진영순%오소원%왕건화
食管肿瘤/调强放射疗法%食管肿瘤/化学疗法%食管肿瘤/靶向疗法%治疗结果
食管腫瘤/調彊放射療法%食管腫瘤/化學療法%食管腫瘤/靶嚮療法%治療結果
식관종류/조강방사요법%식관종류/화학요법%식관종류/파향요법%치료결과
Cetuximab%Esophageal carcinoma/Squamous cell carcinoma%Esophageal carcinoma/Radiation therapy%Radiation therapy/Intensity modulated radiation therapy%Esophageal carcinoma/Chemotherapy
目的 观察西妥昔单抗联合同期放化疗对食管鳞癌的安全性及近期疗效.方法 19例Ⅰ~Ⅲ期无远处转移的食管鳞癌患者入组,西妥昔单抗静脉滴注1次/周,第1周为400 mg/m2,第2~8周为250 mg/m2,每周联合紫杉醇45 mg/m2和顺铂20 mg/m2.第2~8周调强放疗59.4 Gy分33次.结果 2例患者因严重不良反应出组,17例的有效率为100%,其中完全缓解率为71%(12例).中位随访时间29.3个月,1年总生存率、无复发生存率分别为100%,82%.19例患者主要不良反应为骨髓抑制、黏膜反应、皮疹等,其中≥2级粒细胞减少、放射性食管炎、皮疹发生率分别为89%、84%、58%.2例局部复发,1例后颈部淋巴结及肺转移.结论 西妥昔单抗联合同期放化疗对食管鳞癌安全有效,值得扩大样本量进行进一步临床研究.
目的 觀察西妥昔單抗聯閤同期放化療對食管鱗癌的安全性及近期療效.方法 19例Ⅰ~Ⅲ期無遠處轉移的食管鱗癌患者入組,西妥昔單抗靜脈滴註1次/週,第1週為400 mg/m2,第2~8週為250 mg/m2,每週聯閤紫杉醇45 mg/m2和順鉑20 mg/m2.第2~8週調彊放療59.4 Gy分33次.結果 2例患者因嚴重不良反應齣組,17例的有效率為100%,其中完全緩解率為71%(12例).中位隨訪時間29.3箇月,1年總生存率、無複髮生存率分彆為100%,82%.19例患者主要不良反應為骨髓抑製、黏膜反應、皮疹等,其中≥2級粒細胞減少、放射性食管炎、皮疹髮生率分彆為89%、84%、58%.2例跼部複髮,1例後頸部淋巴結及肺轉移.結論 西妥昔單抗聯閤同期放化療對食管鱗癌安全有效,值得擴大樣本量進行進一步臨床研究.
목적 관찰서타석단항연합동기방화료대식관린암적안전성급근기료효.방법 19례Ⅰ~Ⅲ기무원처전이적식관린암환자입조,서타석단항정맥적주1차/주,제1주위400 mg/m2,제2~8주위250 mg/m2,매주연합자삼순45 mg/m2화순박20 mg/m2.제2~8주조강방료59.4 Gy분33차.결과 2례환자인엄중불량반응출조,17례적유효솔위100%,기중완전완해솔위71%(12례).중위수방시간29.3개월,1년총생존솔、무복발생존솔분별위100%,82%.19례환자주요불량반응위골수억제、점막반응、피진등,기중≥2급립세포감소、방사성식관염、피진발생솔분별위89%、84%、58%.2례국부복발,1례후경부림파결급폐전이.결론 서타석단항연합동기방화료대식관린암안전유효,치득확대양본량진행진일보림상연구.
Objective To determine the feasibility and toxicity of the addition of cetuximab to paclitaxel,cisplatin,and concurrent intensity modulated radiation therapy (IMRT) for patients with esophageal squamous cell carcinoma (ESCC).Methods Nineteen patients with stage Ⅰ to Ⅲ ESCC,without distant organ metastases,were eligible.All patients received cetuximab,an initial dose of 400 mg/m2 in the first week followed by weekly injection of 250 mg/m2,paclitaxel 45 mg/m2 and cisplatin 20 mg/m2 weekly for 7 weeks with IMRT of 59.4 Gy/33 fractions.Results Two patients discontinued because of severe adverse events.Seventeen patients completed the planned treatment protocol.Of whom,12 patients achieved completeremission.The objective response rate was 100%.A median follow-up time was 29.3 months.The 1-year overall survival and recurrence-free survival rate was 100% and 82%,respectively.Main toxicities including myelosuppression,esophagitis and skin rash happened in 19 patients.Grade ≥2 neutropenia,esophagitis and skin toxicity noted rates was 89%,84% and 58%,respectively.Local recurrence was found in two patients.Neck lymph node and lung metastasis found in one patient.Conclusions Cetuximab,when combined with paclitaxel,cisplatin and IMRT,is efficient and safe for esophageal squamous cell carcinoma,Further clinical study is needed.