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局限期SCLC超分割或大分割放疗同步化疗预后比较
引用本文:胡晓,夏冰,包勇,徐裕金,王谨,马红莲,金莹,方敏,唐华容,陈梦圆,董百强,傅小龙,陈明.局限期SCLC超分割或大分割放疗同步化疗预后比较[J].中华放射肿瘤学杂志,2017,26(9):1000-1005.
作者姓名:胡晓  夏冰  包勇  徐裕金  王谨  马红莲  金莹  方敏  唐华容  陈梦圆  董百强  傅小龙  陈明
作者单位:310022 杭州,浙江省肿瘤医院放疗科浙江省放射肿瘤学重点实验室(胡晓、徐裕金、王谨、马红莲、方敏、唐华容、陈梦圆、董百强、陈明),化疗科(金莹);杭州市肿瘤医院放疗科,复旦大学附属肿瘤医院放疗科(夏冰);510060 广州,中山大学肿瘤防治中心放疗科(包勇);200030 上海交通大学附属胸科医院放疗科,复旦大学附属肿瘤医院放疗科(傅小龙)胡晓与夏冰贡献相同
基金项目:国家自然科学基金(81402540、81401911、81672972),国家卫生计生委科学研究基金-浙江省医药卫生重大科技计划(省部共建计划)项目(WKJ-ZJ-1701)National Natural Science Foundation of China(81402540
摘    要:目的 比较超分割或大分割放疗同步化疗对局限期SCLC的生存影响。方法 超分割和大分割组分别入组患者92、96例。超分割组采用45 Gy分30次,2 次/d。大分割组采用55 Gy分22次,1 次/d。采用Kaplan-Meier法计算生存率,Cox模型多因素预后分析。结果 超分割和大分割组患者1、2、5年PFS率分别为82%、61%、59%和85%、69%、69%(P=0.27),OS率分别为85%、41%、27%和77%、34%、27%(P=0.37)。多因素分析显示化疗开始到放疗开始时间≤43 d是PFS的有利因素(P=0.005),化疗开始到放疗结束时间≤63 d、PCI是OS有利因素(P=0.044、0.000)。超分割组和大分割组2、3级急性放射性食管炎发生率分别为28%、9%和16%、2%(P=0.009)。结论 采用加速超分割或大分割方案联合同步化疗的PFS及OS均显著提高。控制化疗开始至放疗开始、结束时间≤43 d、≤63 d有利于提高PFS和OS。但2、3级急性放射性食管炎的发生率超分割组显著高于大分割组。

关 键 词:肺肿瘤/放射疗法  放射疗法  调强  放射疗法  超分割  放射疗法  大分割  肺肿瘤/化学疗法  预后  
收稿时间:2017-02-22

Effects of hyperfractionated radiotherapy versus hypofractionated radiotherapy combined with concurrent chemotherapy on prognosis of limited-stage small-cell lung cancer
Hu Xiao,Xia Bing,Bao Yong,Xu Yujin,Wang Jin,Ma Honglian,Jin Ying,Fang Min,Tang Huarong,Chen Mengyuan,Dong Baiqiang,Fu Xiaolong,Chen Ming.Effects of hyperfractionated radiotherapy versus hypofractionated radiotherapy combined with concurrent chemotherapy on prognosis of limited-stage small-cell lung cancer[J].Chinese Journal of Radiation Oncology,2017,26(9):1000-1005.
Authors:Hu Xiao  Xia Bing  Bao Yong  Xu Yujin  Wang Jin  Ma Honglian  Jin Ying  Fang Min  Tang Huarong  Chen Mengyuan  Dong Baiqiang  Fu Xiaolong  Chen Ming
Abstract:Objective To investigate the effects of hyperfractionated radiotherapy versus hypofractionated radiotherapy combined with concurrent chemotherapy on the prognosis of limited-stage small-cell lung cancer (SCLC).Methods A total of 188 patients with limited-stage SCLC were enrolled in this study and divided into hyperfractionated group (n=92) and hypofractionated group (n=96).The hyperfractionated group received thoracic radiotherapy at 45 Gy in 30 fractions twice a day, while the hypofractionated group received 55 Gy in 22 fractions once a day.The Kaplan-Meier method was used to calculate survival rates, and the Cox model was used for multivariate prognostic analysis.Results There were not significant differences in 1-, 2-, and 5-year progression-free survival (PFS) rates and 1-, 2-, and 5-year overall survival (OS) rates between the hyperfractionated group and the hypofractionated group (82% vs.85%, 61% vs.69%, 59% vs.69%, P=0.27;85% vs.77%, 41% vs.34%, 27% vs.27%, P=0.37).The multivariate analysis showed that the time from the initiation of chemotherapy to the initiation of thoracic radiotherapy ≤43 days was favorable prognostic factor for PFS (P=0.005).The time from the initiation of chemotherapy to the end of thoracic radiotherapy ≤63 days and prophylactic cranial irradiation were favorable prognostic factors for OS (P=0.044;P=0.000).There were significant differences in incidence rates of grade 2 and 3 acute radiation esophagitis between the two groups (28% vs.16%, 9% vs.2%, P=0.009).Conclusions Both hyperfractionated radiotherapy and hypofractionated radiotherapy combined with chemotherapy can improve the PFS and OS of patients with limited-stage SCLC.The time from the initiation of chemotherapy to the initiation of thoracic radiotherapy ≤43 days and the time from the initiation of chemotherapy to the end of thoracic radiotherapy ≤63 days are favorable prognostic factors for PFS and OS, respectively.However, the hyperfractionated group has significantly higher incidence rates of grade 2 and 3 acute radiation esophagitis than the hypofractionated group.
Keywords:Lung neoplasms/radiotherapy  Radiotherapy  intensity-modulated  Radiotherapy  hyperfractionation  Radiotherapy  large fractionation  Lung neoplasms/chemotherapy  Prognosis
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