首页> 外文期刊>Radiation oncology >Comparison of efficacy and safety between simultaneous integrated boost intensity-modulated radiotherapy and conventional intensity-modulated radiotherapy in locally advanced non-small-cell lung cancer: a retrospective study
【24h】

Comparison of efficacy and safety between simultaneous integrated boost intensity-modulated radiotherapy and conventional intensity-modulated radiotherapy in locally advanced non-small-cell lung cancer: a retrospective study

机译:局部晚期非小细胞肺癌同时联合加强免疫强度调制放射治疗与常规强度调制放射治疗的疗效和安全性比较:一项回顾性研究

获取原文
           

摘要

Consistent results are lacking as regards the comparative effectiveness of simultaneous integrated boost intensity-modulated radiotherapy (SIB-IMRT) versus conventional intensity-modulated radiotherapy in patients with locally advanced non-small-cell lung cancer (LA-NSCLC). Therefore, we conducted a retrospective analysis to demonstrate the role of SIB-IMRT for patients. Patients who had histologically confirmed NSCLC, stage III disease and received thoracic IMRT between 2014 and 2016 were retrospectively reviewed. The survival, toxicities and dose to organs at risk (OAR) were compared among patients irradiated with different techniques. The SIB-IMRT plans were designed to deliver 45–59.4Gy (median: 50.4Gy) to PTV while simultaneously delivering 50-70Gy (median: 59.92Gy) to PGTV. As for conventional IMRT plans, a total dose of 50-70Gy (median: 60Gy) was delivered to PTV. 426 patients with stage III NSCLC were eligible for analysis, including 128 with SIB-IMRT and 298 with conventional IMRT. The SIB-IMRT group had more stage IIIB disease (69.5% vs. 53%, P?=?0.002), larger planning treatment volumes (median: 504?ml vs. 402?ml, P0.001), and a larger planning treatment volume/volume of lung ratio (median, 0.18 vs. 0.12, P0.001). The median OS of the SIB-IMRT and conventional IMRT groups were 34.5 and 31.7?months, with the 2-year rate of 60.4 and 59%, respectively (P?=?0.797). No difference in PFS, LRFS or DMFS was observed between the two techniques. Patients treated with SIB-IMRT got similar lung and esophageal toxicities versus those with conventional IMRT. SIB-IMRT may be an effective and safe option for patients with locally advanced NSCLC, especially for those with large mass or wide lymph node metastasis.
机译:关于在局部晚期非小细胞肺癌(LA-NSCLC)患者中同时进行的联合加强调强放疗(SIB-IMRT)与常规调强放疗的比较效果,尚缺乏一致的结果。因此,我们进行了回顾性分析,以证明SIB-IMRT对患者的作用。回顾性分析2014年至2016年经组织学证实为NSCLC,III期疾病并接受胸腔IMRT的患者。比较了接受不同技术照射的患者的存活率,毒性和对危险器官的剂量(OAR)。 SIB-IMRT计划旨在向PTV交付45-59.4Gy(中位数:50.4Gy),同时向PGTV交付50-70Gy(中位数:59.92Gy)。至于常规的IMRT计划,总剂量为50-70Gy(中位数:60Gy)已交付给PTV。 426例III期NSCLC患者符合分析条件,包括128例SIB-IMRT和298例常规IMRT。 SIB-IMRT组的IIIB期患病率更高(69.5%vs. 53%,P≥0.002),较大的计划治疗量(中位数:504?ml与402?ml,P <0.001),以及较大的计划治疗体积/肺体积比(中位数,0.18对0.12,P <0.001)。 SIB-IMRT组和常规IMRT组的中位OS分别为34.5和31.7?months,两年率分别为60.4和59%(P≥0.797)。两种技术之间未观察到PFS,LRFS或DMFS的差异。与传统IMRT相比,接受SIB-IMRT治疗的患者的肺和食道毒性相似。对于患有局部晚期NSCLC的患者,特别是对于具有大量或广泛淋巴结转移的患者,SIB-IMRT可能是一种有效且安全的选择。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号