...
首页> 外文期刊>Annals of surgical oncology >Concurrent Selective Lymph Node Radiotherapy and S-1 Plus Cisplatin for Esophageal Squamous Cell Carcinoma: A Phase II Study
【24h】

Concurrent Selective Lymph Node Radiotherapy and S-1 Plus Cisplatin for Esophageal Squamous Cell Carcinoma: A Phase II Study

机译:同时选择性淋巴结放射治疗和S-1加上食管鳞状细胞癌的顺铂:II期研究

获取原文
获取原文并翻译 | 示例

摘要

BackgroundThe efficacy, toxicity, and patterns of failure of esophageal squamous cell carcinoma (ESCC) treated with selective lymph node (SLN) conventional fraction radiotherapy (CFRT) and S-1 plus cisplatin (CDDP) were evaluated.Patients and Methods67 Patients with clinical stage II-IVa ESCC were enrolled. The total dose of SLN CFRT was 60Gy in 30 fractions over 6weeks. The first course of radiation covered the primary and metastatic regional tumors and high-risk lymph nodal regions, given at 2Gy/fraction for a dose of 40Gy. In the second course, CFRT was delivered to the boost volume for an additional 20Gy in 10days, using 2Gy/fraction. Two cycles of chemotherapy were given at the beginning of radiotherapy. CDDP at 25mg/m(2)/day was given on days 1-3 and days 22-24, and S-1 at 80mg/m(2)/day on days 1-14 and days 22-35. Patients achieving objective response after concurrent chemoradiotherapy underwent two additional cycles of chemotherapy.ResultsThe objective response rate (ORR) was 82.5%. Grade 3 or 4 toxicities included leukopenia (23.8%), neutropenia (14.3%), thrombocytopenia (14.3%), hemoglobin (4.8%), gastrointestinal (12.7%), skin (1.6%), and esophagus fistula (1.6%). One patient died of severe pneumonia, and two died of late toxicity because of esophagus fistula. With median follow-up of 32months, the overall survival (OS) and progression-free survival (PFS) at 1year and 2years were 81.0% and 73.0%, and 63.5% and 49.2%, respectively.ConclusionsSLN RT concurrent with S-1 plus CDDP may represent a better strategy for treatment of ESCC patients.
机译:背景技术用选择性淋巴结(SLN)常规分数放射治疗(CFRT)和S-1加顺铂(CDDP)处理的食管鳞状细胞癌(ESCC)失败的疗效,毒性和模式进行评估。患者和方法67临床阶段患者II-IVA ESCC注册。 SLN CFRT的总剂量为30码,30级以上超过6周。第一种辐射过程覆盖了主要和转移性区域肿瘤和高风险淋巴结区域,在2Gy /级分中给予了一剂40Gy。在第二课程中,使用2Gy /分数,在10天内将CFRT递送至升压体积,以便在10天内额外20Gy。在放疗开始时给出了两个化疗的两个循环。在25mg / m(2)/日为25mg / m(2)/天的CDDP在第1-3天和第22-24天,并且S-1在80mg / m(2)/天/天1-14和22-35天。同时化疗后达到客观反应的患者进行了两次额外的化疗循环。物理反应率(ORR)为82.5%。 3级或4级毒性包括白细胞减少(23.8%),中性粒细胞蛋白(14.3%),血小板减少(14.3%),血红蛋白(4.8%),胃肠道(12.7%),皮肤(1.6%)和食道瘘(1.6%)。一名患者死于严重的肺炎,由于食道瘘,两次死于晚期毒性。中位后32个月的后续随访,1年和2年的整体存活率(OS)和无进展生存(PFS)分别为81.0%和73.0%,分别为63.5%和49.2%。与S-1加上同时连接。 CDDP可以代表ESCC患者治疗更好的策略。

著录项

  • 来源
    《Annals of surgical oncology 》 |2019年第6期| 共7页
  • 作者单位

    Shandong Univ Dept Radiat Oncol Shandong Canc Hosp Jinan Shandong Peoples R China;

    Shandong Univ Dept Radiat Oncol Shandong Canc Hosp Jinan Shandong Peoples R China;

    JiMo Peoples Hosp Dept Thorac Surg Qingdao Shandong Peoples R China;

    Qingdao Hiser Med Ctr Dept Gastroenterol Qingdao Shandong Peoples R China;

    Shandong Univ Dept Radiat Oncol Shandong Canc Hosp Jinan Shandong Peoples R China;

    Shandong Univ Dept Radiat Oncol Shandong Canc Hosp Jinan Shandong Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 外科学 ;
  • 关键词

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