期刊文献+

同步整合加量调强放射治疗原发性食管癌的临床疗效 被引量:4

Clinical efficacy of simultaneous integrated boost intensity-modulated radiation therapy for primary esophageal cancer
下载PDF
导出
摘要 目的:评价同步整合加量调强放射治疗(SIB-IMRT)技术治疗原发性食管癌的近期疗效及不良反应。方法32例原发性食管癌患者均采用5野或7野的 SIB-IMRT 技术进行放射治疗。肿瘤靶区(GTV)220 cGy/F,总剂量6600 cGy/30F;临床靶区(CTV)单次剂量180 cGy,总剂量5400 cGy/30F。结果32例原发性食管癌患者均按计划完成放射治疗。放射治疗结束时有26例患者食管病灶完全缓解,完全缓解率为81%(26/32);4例部分缓解,部分缓解率为13%。右肺 V20为9%-21%,左肺 V20为11%-23%。其中Ⅰ-Ⅱ级放射性食管炎共11例,发生率为34%。Ⅰ-Ⅱ级放射性气管炎6例,发生率为19%,无Ⅲ级以上急性不良反应发生。结论SIB-IMRT 技术治疗原发性食管癌疗效好,不良反应可耐受。 Objective To evaluate the short-term efficacy and adverse events of simultaneous inte-grated boost intensity-modulated radiation therapy (SIB-IMRT)in the treatment of primary esophageal cancer. Methods Thirty-two patients diagnosed with primary esophageal cancer were treated with 5-or 7-field SIB-IM-RT.Gross target volume (GTV)was given at a dose of 220 cGy/F with a total dose of 6 600 cGy/30F.Clini-cal target volume (CTV)was given at a single dose of 180 cGy/F with a total dose of 5 400 cGy/30F.Results All 32 patients successfully completed the chemotherapy.The complete response rate was 81% (26 /32)and partial response rate was 13% (4 /32).The V20 of the left lung ranged from 11% to 23% and 9%-21% for the V20 of the right lung.Eleven patients (34%)presented with grade Ⅰ-Ⅱ radiation esophagitis and 6 (19%)had grade Ⅰ-Ⅱ radiation tracheitis.Conclusions SIB-IMRT is an effective therapy in treating pri-mary esophageal cancer and the adverse events are tolerable.
出处 《新医学》 2015年第1期20-23,共4页 Journal of New Medicine
关键词 食管癌 放射治疗 同步整合加量 调强放射治疗 Esophageal cancer Radiotherapy Simultaneous integrated boost Intensity-modulated radiation therapy
  • 相关文献

参考文献7

二级参考文献62

共引文献373

同被引文献39

  • 1Oyama T. Diagnostic strategies of superficial Barrett e- sophageal cancer for endoscopic submucosal dissection. Dig Endosc, 2013, 25 (Suppl 1) : 7-12.
  • 2Patel V, Burbridge RA. Endoscopic approaches for ear- ly-stage esophageal cancer: current options. Curr Oncol Rep, 2015, 17 (1): 421.
  • 3Kawaguchi G, Sasamoto R, Abe E, Ohta A, Sato H, Tanaka K, Maruyama K, Kaizu M, Ayukawa F, Yama- na N, Liu J, Takeuchi M, Kobayashi M, Aoyama H. The effectiveness of endoscopic submucosal dissection followed by chemoradiotherapy for superficial esophageal cancer. Radiat Oncol, 2015, 10: 31.
  • 4Wong R, Malthaner R. Combined chemotherapy and radiotherapy (without surgery) compared with radiotherapy alone in localized carcinoma of the esophagus[ J ]. Cochrane Database Syst Rev, 2006, ( 1 ) :CD002092.
  • 5Bos LI, Damen EM, de Boer RW, et al. Reduction of rectal dose by integration of the boost in the large-field treatment plan for prostate irradiation[J]. Int J Radiat Oneol Biol Phys, 2002,52 ( 1 ) :254-265.
  • 6Wu Q, Manning M, Schmidt-Ullrieh R, et al. The potential for sparing of parotids and escalation of biologically effective dose with intensity-modulated radiation treatments of head and neck cancers : a treatment design study[J]. Int J Radiat Oncol Biol Phys, 2000, 46( 1 ) : 195-205.
  • 7Welsh J, Palmer MB, Ajani JA, et al. Esophageal cancer dose escalation using a simultaneous integrated boost technique[ J]. Int J Radiat Oncol Biol Phys, 2012,82 ( 1 ) : 468-474. DOI: 10. 1016/j. ijrobp. 2010.10. 023.
  • 8Ramos TC, Figueredo J, Catala M, et al. Treatment of high-grade glioma patients with the humanized anti-epidermal growth factor receptor (EGFR) antibody h-R3 : report from a phase I / lI trial [J]. Cancer Biol Ther, 2006,5(4) :375-379.
  • 9Bebb G, Smith C, Rorke S, et al. Phase clinical trial of the anti-EGFR monoclonal antibody nimotuzumab with concurrent external thoracic radiotherapy in Canadian patients diagnosed with stage Ⅱ b, Ⅲ or 1V non-small cell lung cancer unsuitable for radical therapy[ J]. Cancer Chemother Pharmacol, 2011 ,67 (4) : 837-845. DOI: 10. 1007/s00280-010-1379-9.
  • 10Ramos-Suzarte M, Lorenzo-Luaces P, Lazo NG, et al. Treatment of malignant, non-resectable, epithelial origin esophageal tumours with the humanized anti-epidermal growth factor antibody nimotuzumab combined with radiation therapy and chemotherapy [J]. Cancer Biol Ther, 2012,13(8) :600-605. DOI: 10.4161/ cbt. 19849.

引证文献4

二级引证文献42

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部