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重组人血管内皮抑素联合同步放化治疗局部晚期非小细胞肺癌
引用本文:丁颖,王希成,杨帆,林丽珠,刘亦敏,杨曙,刘晓清,彭苗,陈斯泽.重组人血管内皮抑素联合同步放化治疗局部晚期非小细胞肺癌[J].广东药学院学报,2011,27(2):202-206.
作者姓名:丁颖  王希成  杨帆  林丽珠  刘亦敏  杨曙  刘晓清  彭苗  陈斯泽
作者单位:1. 广东药学院附属第一医院肿瘤科,广东,广州,510080
2. 广州中医药大学附属医院肿瘤科,广东,广州,510160
3. 中山大学附属第二医院放疗科,广东,广州,510120
基金项目:广东省医学科学技术研究基金
摘    要:目的 评估重组人血管内皮抑素(恩度)联合多西紫杉醇与顺铂同步放化治疗局部晚期非小细胞肺癌的近期疗效及不良反应.方法 28例经组织学确诊符合入组条件的ⅢA或ⅢB非小细胞肺癌患者随机分成试验组和对照组,每组14例.试验组采用恩度联合同步放化疗,对照组采用同步放化疗,观察两组的疗效及不良反应.结果 试验组、对照组放后的缓解率...

关 键 词:非小细胞肺癌  血管内皮抑素/恩度  同步放化疗  多西紫杉醇  顺铂  不良反应

Recombinant human endostatin combined with concurrent chemoradiotherapy in treatment of locally advanced non-small cell lung cancer
DING Ying,WANG Xi-cheng,YANG Fan,LIN Li-zhu,LIU Yi-min,YANG Shu,LIU Xiao-qing,PENG Miao,CHEN Si-ze.Recombinant human endostatin combined with concurrent chemoradiotherapy in treatment of locally advanced non-small cell lung cancer[J].Academic Journal of Guangdong College of Pharmacy,2011,27(2):202-206.
Authors:DING Ying  WANG Xi-cheng  YANG Fan  LIN Li-zhu  LIU Yi-min  YANG Shu  LIU Xiao-qing  PENG Miao  CHEN Si-ze
Institution:1(1.Department of Oncology,The First Affiliated Hospital of Guangdong Pharmaceutical College,Guangzhou,Guangdong 510080,China;2.Department of Oncology,Guangzhou University of Chinese Medicine,Guangzhou,Guangdong 510160,China;3.Department of Radiation Oncology,The Second Affiliated Hospital of Sun Yat-sen University,Guangzhou,Guangdong 510120,China)
Abstract:Objective To evaluate the efficacy and safety of docetaxel and cisplatin (DP) concurrent chemoradiotherapy combined with recombinant human endostatin (endostar) in patients with inoperable locally advanced non-small-cell lung cancer (LANSCLC). Methods A total of 28 patients diagnosed with inoperable LANSCLC (ⅢA or Ⅲ B) were randomly divided into two groups . Patients of the experimental group(n = 14) were treated with endostar combined DP chemotherapy (docetaxel 75 mg/m2 on day 1, cisplatin 20 mg/m2 on day 1 -4 and endostar 15 mg/d on day 1 - 14 ,repeated every 3 -4 weeks and with 3 to 4 cycles) and concurrent thoracic radiotherapy while the patients of the control group( n = 14) were treated with DP concurrent chemoradiotherapy only. The primary tumors and involved lymph nodes wereadministrated three-dimensional conformal radiotherapy (3DCRT) at a total dose of 50 to 60 Gy (200 cGy! fraction ,51Yweek, completed in 5 to 6 weeks) to all patients. After 4 -6 weeks patients with residual tumor lesions received additional stereotactic body radiotherapy(SBRT) at the doses of 18 -27 Gy (300 cGy/ fraction, every other day) not beyond the tolerated doses of surrounding important normal organs. The efficacy was evaluated according to RECIST criteria. The adverse reactions were evaluated according to NCI CTC3.0 criteria and RTOG/EORT radiation reaction criteria. Results The response rate ( CR + PR) was 71.4% in the experimental group and 64.3% in control group after 3DCRT(P 〉 O. 05). Though the overall response rate raised after SBRT in both groups (85.71% vs 78.57% ), the diversities were not significant(P 〉 0. 05 ). Till last follow-up day, time to progression (TIP) and 1-year progression free survival rate and 1-year overall survival rate and median survival time (MST) in experimental group myelosuppression and control group were 13.0 m vs 11.8 m,64.3% vs 57.1% ,78.6% vs 85.7% and 21.1 m vsl9.8 m respectively without significant difference (P 〉 0.05 ). The main adverse reactions of both groups include , nausea and vomiting, grade 1 to 2 acute radiation pneumonitis and acute radiation esophagitis ( P 〉 0. 05 ). Though the experimental group patients were observed with more transient cardiovascular adverse reactions ,the diversities were not significant( P 〉 0.05 ). All the adverse reactions could be relieved and tolerated after appropriate treatment. Both group patients were not observed with hemorrhage,grade g hematoblast depression, grade 3 to 4 acute radiation pneumonitis and acute radiation esophagitis. Conclusion The concurrent chemoradiotherapy (based on 3DCRT) of docetaxel and cisplatin combined with recombinant human endostatin (endostar) can be considered as an effective and feasible approach for the treatment of chosen inoperable LANSCLC.
Keywords:non-small cell lung cancer  NSCLC  endostatin  endostar  concurrent chemoradiotherapy  docetaxel  cisplatin  adverse reaction
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