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食管癌术后复发患者调强放疗同步化疗(5-Fu+奈达铂)的Ⅱ期临床研究[J]. 肿瘤防治研究, 2012, 39(10): 1261-1264. DOI: 10.3971/j.issn.1000-8578.2012.10.026
引用本文: 食管癌术后复发患者调强放疗同步化疗(5-Fu+奈达铂)的Ⅱ期临床研究[J]. 肿瘤防治研究, 2012, 39(10): 1261-1264. DOI: 10.3971/j.issn.1000-8578.2012.10.026
Phase Ⅱ Study of Intensity-Modulated Radiotherapy Combined with 5-Fluorouracil and Nedaplatin Chemotherapy in Recurrent Esophageal Carcinoma after Curative Operation[J]. Cancer Research on Prevention and Treatment, 2012, 39(10): 1261-1264. DOI: 10.3971/j.issn.1000-8578.2012.10.026
Citation: Phase Ⅱ Study of Intensity-Modulated Radiotherapy Combined with 5-Fluorouracil and Nedaplatin Chemotherapy in Recurrent Esophageal Carcinoma after Curative Operation[J]. Cancer Research on Prevention and Treatment, 2012, 39(10): 1261-1264. DOI: 10.3971/j.issn.1000-8578.2012.10.026

食管癌术后复发患者调强放疗同步化疗(5-Fu+奈达铂)的Ⅱ期临床研究

Phase Ⅱ Study of Intensity-Modulated Radiotherapy Combined with 5-Fluorouracil and Nedaplatin Chemotherapy in Recurrent Esophageal Carcinoma after Curative Operation

  • 摘要: 目的 评价食管癌根治术后复发患者调强放疗同步化疗(5-Fu+奈达铂)的近期疗效和不良反应。方法选取2009年6月—2010年6月44例符合入组条件的食管癌术后复发患者,均采用调强放疗同步化疗(5-Fu+奈达铂)方案进行治疗。调强放疗:GTV给量60 Gy/30 f,2.0 Gy/f;CTV给量54 Gy/30 f,1.8 Gy/f。同步化疗在放疗的第1周和第4周进行,具体为:5-Fu 750 mg/(m2·d),d1~5,奈达铂80 mg/(m2·d),d1。主要观察终点是1年生存率,次要观察终点是不良反应。结果全组总有效率为86%(38/44)。1年和2年总生存率分别为72.7%和60%。1年和2年无进展生存率分别为63.6%和36.6%。放化疗期间出现Ⅰ、Ⅱ和Ⅲ度骨髓抑制的患者分别为16%(7/44)、50%(22/44)和34%(15/44);出现Ⅰ度和Ⅱ度胃肠道反应的患者分别为45%(20/44)、55%(24/44);出现Ⅰ度和Ⅱ度肝/肾功能生化指标异常的患者分别为77%(34/44)、23%(10/44),未发现Ⅲ度及以上胃肠道及肝/肾功能生化指标异常者。所有不良反应经对症处理后均好转,全组患者均顺利完成放化疗计划,无疗程中断或延迟者。结论食管癌根治术后复发患者进行调强放疗同步化疗(5-Fu+奈达铂)的近期疗效好,不良反应小,值得进行Ⅲ期临床研究。

     

    Abstract: Objective To analyze the feasibility and safety of postoperative recurrent esophageal carcinoma patients treated by intensity-modulated radiotherapy combined with 5-Fluorouracil(5-Fu) and nedaplatin chemotherapy. Methods Forty-four esophageal carcinoma patients suffered recurrence after their definitive resection in our department from June 2009 to June 2010.Intensity-modulated radiotherapy combined with 5-Fu and nedaplatin chemotherapy was performed in the patients(gross tumor volume,GTV) of IMRT was prescribed to 60 Gy/30f,2.0 Gy/f and 5-Fu and nedaplatin concurrent chemotherapy was used by 5-Fu 750 mg/(m2·d),d1~5,nedaplatin 80 mg/(m2·d),d1 at week 1 and week 4.The primary endpoint was 1-year survival rate and the second endpoint was toxicity related to the treatment. Results The overall response rate (CR+PR) was 86%(38/44).1- and 2-year overall survival rate was 72.7% and 60%,respectively.1- and 2-year progression-free survival rate was 63.6% and 36.6%,respectively.Univariate analysis outcome showed that only recurrent site was related with prognosis (χ2=22.848,P=0.000).All the patients undergone this treatment smoothly.Grade Ⅰ,Ⅱ and Ⅲ leukocytopenia was observed in 16% (7/44),50% (22/44),and 34% (15/44) patients,respectively.Grade I,and II digestive tract toxicity was observed in 45% (20/44),55% (24/44) patients,respectively.Grade Ⅰ,and Ⅱ liver/renal toxicity was observed in 77% (34/44),and 23% (10/44) patients,respectively.Over grade 3 digestive tract and liver/renal toxicity were not found.All the toxicities were gone after corresponding therapy. Conclusion Concurrent chemotherapy with 5-Fu and nedaplatin plus intensity-modulated radiotherapy is an effective and feasible regimen and would be considered as a better option for postoperative recurrent esophageal carcinoma patients,which could be deserved to be applied to phase Ⅲ clinical trial.

     

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