郝俊芳, 董伟, 徐瑾, 杨新华, 钱明, 于水, 姚春萍, 刘兰平. 后程超分割调强放疗联合化疗治疗中晚期鼻咽癌的临床研究[J]. 中国肿瘤临床, 2011, 38(7): 400-404 . DOI: 10.3969/j.issn.1000-8179.2011.07.010
引用本文: 郝俊芳, 董伟, 徐瑾, 杨新华, 钱明, 于水, 姚春萍, 刘兰平. 后程超分割调强放疗联合化疗治疗中晚期鼻咽癌的临床研究[J]. 中国肿瘤临床, 2011, 38(7): 400-404 . DOI: 10.3969/j.issn.1000-8179.2011.07.010

后程超分割调强放疗联合化疗治疗中晚期鼻咽癌的临床研究

  • 摘要: 目的:评价后程超分割放疗联合化疗治疗Ⅲ~Ⅳa期鼻咽癌的疗效。方法: 60例Ⅲ~Ⅳa期鼻咽癌采用随机分组为常规组、 后程超分割同步化疗组。均先采用面颈联合野常规分割对穿照射40 Gy, 20次4周完成。后超组缩野后改用后程超分割调强放疗, 1.2 Gy/次, 2次/天, 共14~15天完成。鼻咽病灶总DT 73.6~76 Gy/7周。且在放疗同时给予PF方案治疗。对照组缩野后给予常规照射2 Gy/次, 鼻咽病灶DT 70~74 Gy/35~37次/7~7.5周。结果: 后程超分割调强放疗同步化疗组与常规组肿瘤消退率分别为96.6% (29/30)、 93.3% (28/30)(P>0.05), 1、 3年肿瘤局部控制率分别为93.1%、 89.6%和82.1%、 67.8%。1、 3年生存率分别为96.5%、 93.1%和92.8%、 71.4% (P<0.05)。后程超分割调强放疗同步化疗组的急性放疗反应显著高于常规分割放疗组。远期不良反应如口干及颈部软组织纤维化低于常规分割放疗组。结论: 后程超分割调强放疗可提高局部晚期鼻咽癌的局控率及生存率,放化疗结合可降低远处转移率, 毒副反应可耐受。

     

    Abstract: Treatment of Stage Ⅲ-Ⅳa Nasopharyngeal Carcinoma with Combined Late CourseAccelerated Hyperfractionation Radiotherapy and ChemotherapyJunfang HAO,Wei DONG, Jin XU, Xinhua YANG, Ming QIAN, Shui YU, Chunping YAO, Lanping LIUCorrespondence to: Lanping LIU, E-mail: 29294521@qq.comThe Third Department of Radiotherapy, Shandong Provincial Tumor Hospital, Ji’ nan 250117, ChinaAbstract Objective: To evaluate the clinical effects of the combined late course accelerated hyperfractionation radiotherapy(LCAHR) and chemotherapy on stageⅢ-Ⅳa nasopharyngeal carcinoma (NPC). Methods: A total of 60 NPC patients with stageⅢ-Ⅳadisease were randomly divided into the conventional control group (group A) treated with traditional fractionated radiotherapy, and thestudy group (group B) treated with LCAHR combined with chemotherapy. A traditional irradiation of 40 Gy at the two opposing fa-cial-cervical anterior-posterior fields (AP-PA) was conducted in both groups, with 20 fractions completed within 4 weeks. After reduc-tion of the irradiated field, LCAHR was performed in group B with a dose of 1.2Gy/f, 2 fractions a day at a 4-6 hour interval, for 14-15days. The total dose for NPC was 73.6Gy~76Gy in 7 weeks. Chemotherapeutic PF regimen was administered concurrently with radio-therapy. Group A received conventional radiotherapy with a total dose of 70Gy~74Gy for 7 - 7.5 weeks. Results: The rate of completeregression of NPC was 96.6% (29/30) in group B and 93.3% (28/30) in group A at the end of the course (P>0.05). The 1- and 3-year lo-cal control rates in group B and group A were 93.1% and 89.6%, and 82.1% and 67.8%, respectively . The 1- and 3- year survival rateswere 96.5% (28/29) and 93.1% (27/29) in group B, and 92.8% (26/28) and 71.4% (20/28) in group A (P< 0.05). The incidence of acuteradiation response was obviously higher in group B than in group A. The incidences of long-term adverse reactions, such as dry mouthand fibrosis of the soft tissues of the neck, were lower in group B than in group A. Conclusion: LCAHR can improve the local controlrate and the survival rate of NPC patients. Combining LCAHR with chemotherapy can reduce distant metastasis of NPC, with tolerableadverse reactions.Keywords Nasopharyngeal carcinoma; Late course accelerated hyperfractionated radiotherapy; Chemotherapy

     

/

返回文章
返回